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Exposure to Animal Feces and Human Health: A Systematic Review and Proposed Research Priorities
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Exposure to Animal Feces and Human Health: A Systematic Review and Proposed Research Priorities
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Department of Environmental Health, Emory University, Atlanta, Georgia 30322 United States
*Phone: (404) 712-8767; e-mail: [email protected]
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Environmental Science & Technology

Cite this: Environ. Sci. Technol. 2017, 51, 20, 11537–11552
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https://doi.org/10.1021/acs.est.7b02811
Published September 19, 2017

Copyright © 2017 American Chemical Society. This publication is licensed under CC-BY.

Abstract

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Humans can be exposed to pathogens from poorly managed animal feces, particularly in communities where animals live in close proximity to humans. This systematic review of peer-reviewed and gray literature examines the human health impacts of exposure to poorly managed animal feces transmitted via water, sanitation, and hygiene (WASH)-related pathways in low- and middle-income countries, where household livestock, small-scale animal operations, and free-roaming animals are common. We identify routes of contamination by animal feces, control measures to reduce human exposure, and propose research priorities for further inquiry. Exposure to animal feces has been associated with diarrhea, soil-transmitted helminth infection, trachoma, environmental enteric dysfunction, and growth faltering. Few studies have evaluated control measures, but interventions include reducing cohabitation with animals, provision of animal feces scoops, controlling animal movement, creating safe child spaces, improving veterinary care, and hygiene promotion. Future research should evaluate: behaviors related to points of contact with animal feces; animal fecal contamination of food; cultural behaviors of animal fecal management; acute and chronic health risks associated with exposure to animal feces; and factors influencing concentrations and shedding rates of pathogens originating from animal feces.

Copyright © 2017 American Chemical Society

Introduction

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Nearly two-thirds of human pathogens and three-quarters of emerging pathogens are zoonotic in origin. (1, 2) While research has focused on zoonotic transmission of respiratory and vector-borne pathogens, such as Ebola and West Nile Virus, less attention has been given to pathogens found in animal feces that are transmitted via water, sanitation, and/or hygiene (WASH)-related pathways, as illustrated by the classic “F-diagram” (Figure 1). (3) According to the Food and Agricultural Organization (FAO), “domestic animals such as poultry, cattle, sheep, and pigs generate 85% of the world’s animal faecal waste, proportionally a far greater amount than the contribution by the human population”; the fecal production rate can total to 2.62 × 1013 kg/year. (4) Insufficient separation of animal feces from human domestic environments, common in low-income countries, can lead to fecal-oral transmission of zoonotic pathogens through direct contact with humans and/or fecal contamination of fingers, food, and water sources.

Figure 1

Figure 1. Traditional F-Diagram showing potential fecal-oral transmission pathways. Adapted from Wagner, E.; Lanoix, J., Excreta disposal for rural areas and small communities. Monograph Series World Health Organization.1958, 39, 182. Copyright 1958, World Health Organization.

Several pathogens of zoonotic origin are associated with acute gastrointestinal symptoms that can arise from contact with animal feces. (5) Children may experience long-term growth shortfalls after exposure to these pathogens, and pregnant women and the immunocompromised may also experience severe and/or long-term adverse health effects after infection with pathogens carried in animal feces. (6-9) Approximately one-third of deaths among children under five years due to diarrhea in the Global Burden of Disease 2015 report are attributed to pathogens that can be found in animal feces. (10) While some studies seek to identify a relationship between animal contact and diarrhea, not all etiologies of diarrhea are transmitted through animal feces. While many important viral enteropathogens (e.g., rotavirus) have limited zoonotic transmission, animal feces may play an important role in the transmission of some important etiologies of childhood diarrhea, such as Cryptosporidium, which substantially contributes to the childhood burden of diarrheal disease and has been associated with severe acute and long-term clinical manifestations, including child growth faltering. (11) Unlike rotavirus, there is currently no vaccine for Cryptosporidium and treatment options are limited and often unavailable in developing countries. Thus, preventive measures for such zoonotic pathogens are important for reducing disease burden. Though the total contribution of zoonotic transmission is unknown, it may be substantial, and it may vary by the virulence and animal host(s) of the specific etiologic agent, geographic and cultural context, and environmental conditions. (12)
Recent reviews, predominantly using observational data, suggest that improved WASH conditions are associated with better children’s health outcomes. (13-15) Yet randomized controlled trials in low-income rural settings have demonstrated mixed effects of such interventions on diarrhea, soil-transmitted helminth (STH) infection, trachoma, and stunting. (16-23) Even comprehensive WASH interventions may be insufficient to prevent growth faltering in rural settings. (24) One possible reason for the lack of health effects is suboptimal program fidelity and adherence, yielding less than universal coverage and use. (25) An alternative explanation is that because sanitation interventions have focused primarily on containment of human excrement, the lack of evidence for health effects in large intervention trials could be due to persistent exposure to fecal pathogens of animal origin among the study populations. (5, 26, 27) A recent systematic review and meta-analysis noted that domestic poultry and livestock exposure are associated with diarrheal illness in humans; (5) we expand on this review by exploring the risk of animal exposure on diarrhea, child growth outcomes, environmental enteric dysfunction (EED), pathogenic infection, trachoma, and STH infection.
Human exposure to animal feces is more common in developing countries where domestic animals and their animal feces may not be properly contained or separated from domestic environments. Though children and adults in high-income countries (HIC) can also be exposed to animals and/or their feces, potentially causing bacterial, helminth, and/or protozoan infections, (28-33) the risk may be greater in low- and middle-income countries (LMIC), where domestic animal ownership and middle- and small-scale animal production is more common in both rural and urban households (34) compared to households in HIC.
The primary objective of this systematic review was to examine what is known about human health impacts of exposure to poorly managed animal feces transmitted via WASH-related pathways in LMIC. We identified and synthesized existing literature to assess the extent to which exposure to poorly managed animal feces could affect health outcomes in humans. We modified the traditional “F-diagram” to focus on animal feces exposure in households and small-scale animal operations, in households with pets, and in communities with synanthropic rodents; through this lens we propose research priorities to better understand human exposure to poorly managed animal feces. We identified interventions that have been used to control human exposure to animal feces and summarized what is known about their effectiveness in reducing the presence of animal feces in the environment, preventing human exposure to animal feces, and/or limiting negative human health outcomes. Based on this review, we identified a set of priority research areas to improve our understanding of the human health burden associated with exposure to animal feces, with the ultimate goal of identifying potential control measures to reduce this burden in LMIC.

Materials and Methods

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Search Strategy

To assess the impacts of animal feces on human health, we searched for papers with terms for “animals, feces, exposure, and humans” (Supporting Information (SI) 1, p. 2). The search was limited to English- and Spanish-language studies and included papers published before October 3, 2016. We searched in the following databases: PubMed, Web of Science, Cochrane Library, EMBASE, and CAB Direct. We also included a partial search of the Environmental Sciences and Pollution Management (ESPM) database, but due to host database server challenges at the time of the search, 26% of full search results from this database could not be downloaded. We conducted a search of gray literature in International Food Policy Research Institute (IFPRI), Consultative Group on International Agricultural Research (CGIAR), International Livestock Research Institute (ILRI), Food and Agriculture Organization of the United Nations (FAO), U.S. Centers for Disease Control and Prevention (CDC), and the World Health Organization (WHO). We also included papers from personal libraries and literature collections, including a limited number of highly relevant studies that were published between October 2016 and September 2017. We included experimental and observational study designs. All study settings and populations were eligible for inclusion.

Selection of Studies

Search results were cataloged and organized in EndNote X7 (Clarivate Analytics, Boston, MA). Four researchers (GP, JS, LM, BW) examined every publication’s title and abstract to assess if the publication met one or more of the following inclusion criteria: (a) human exposure to poorly managed animal feces; (b) negative human health outcomes from exposure to animal feces (e.g., diarrhea, gastroenteritis, EED, trachoma, STH infections, child growth (anthropometric) outcomes, and infection by zoonotic pathogens); and (c) animal feces contamination of the environment (e.g., water or fields). First, the four researchers all independently reviewed an initial 150 publications to ensure consistency among the study team when determining if papers met the above inclusion criteria. Afterward, the remaining search results were divided equally among the four researchers who independently reviewed the title and abstract of their designated search results. We define poorly managed feces as animal feces that are not contained or separated from human domestic and public environments. We define exposure to animal feces as behaviors related to handling animal feces (e.g., spreading manure on fields or removing domesticated cat feces from litter) and human activity conducted in close proximity to animals and their feces (e.g., children playing on the ground where chickens also roam). While identifying publications that met the inclusion criteria, we simultaneously identified papers that discussed animal husbandry practices and animal feces/manure management, and we identified papers that discussed control measures for reducing human exposure to animal waste. If researchers were unable to make a decision about including or excluding a publication during the title and abstract review process, the publication’s features were discussed among the four researchers and a decision was made.
We excluded publications that discussed one or more of the following: no exposure to animals or animal feces, exposure to animal or animal feces in occupational or industrial settings (e.g., commercial farms), exposure to animal urine, animal health outcomes, human respiratory health outcomes, and diseases related to exposure to insect feces (e.g., Chagas Disease). We excluded papers from HIC because piped sanitation and piped water infrastructure are prevalent, and we wanted to explore how humans are exposed to animal feces in LMIC where sanitation and water infrastructure may be limited or nonexistent.
Two researchers (GP, JS) reviewed the full-text of publications that met the inclusion criteria to confirm the publication met the inclusion criteria as well as one of the following: (a) risk factors, such as exposure to or contact with animals or animal feces, associated with zoonotic infection; (b) animal husbandry practices/behaviors and information about animal feces management; or (c) control measures or interventions aimed at reducing human exposure to animal waste. Other areas of potential interest that were beyond the scope of this review include papers that focused on the epidemiology and etiology, antibiotic resistance, or animal shedding of zoonotic fecal pathogens. No publications from the gray literature met our inclusion criteria for this review.

Data Extraction and Synthesis

Data from papers deemed to meet the inclusion criteria were extracted into a prepiloted extraction form, which included research objectives, key findings, descriptions of study populations, descriptions of health outcomes, and descriptions of exposures to animals and/or their feces (SI Table S1). During synthesis, data were classified by health outcomes, pathogens of concern, exposures to common domestic animals, and regions in which the studies were conducted. Health outcomes, such as diarrhea and trachoma, were assessed by individual studies in a variety of methods including recall, health professional diagnosis, and/or testing. Publications that discussed control measures to remove or reduce the presence of animal feces were identified and classified according to control approach. We did not conduct a meta-analysis or a risk of bias assessment because of the heterogeneity of methods, exposures, and outcomes used across the studies included in the review. We conducted the systematic review according the evidence-based minimum requirements identified by the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) checklist (SI Table S2). (35)

Results & Discussion

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Our search yielded 12 425 unique results, of which the full texts of 329 articles were reviewed. A total of 62 publications met the inclusion criteria (SI Figure S1). Characteristics of publications included in this review are summarized in Table 1 (regions, health outcomes, and animals) and Table 2 (pathogens).
Table 1. Summary of Characteristics of Studies (n = 62)a Included in Review of Potential Health Impacts from Exposure to Animal Feces
Regionn (%)
Africa 
North Africa1 (2%)
Sub-Saharan Africa19 (31%)
Asia 
Middle East1 (2%)
South Asia19 (31%)
Southeast Asia9 (15%)
East Asia1 (2%)
South America12 (19%)
Oceania1 (2%)
Global1 (2%)
Health Outcomesn (%)
Diarrhea18 (29%)
Environmental Enteric Dysfunction2 (3%)
Helminth Seropositivity5 (8%)
Mortality1 (2%)
Nutrition and Growth Outcomes8 (13%)
Pathogens Found in Stool17 (27%)
Trachoma3 (5%)
Hookworm-Related Cutaneous Larva Migrans1 (2%)
Other: human behaviors/practices5 (8%)
No Health Outcomes Specified14 (23%)
Animaln (%)
Livestock 
Buffalo5 (8%)
Cattle25 (40%)
Goats19 (30%)
Sheep14 (22%)
Pigs9 (14%)
Poultry (chickens, ducks, geese, quail)29 (46%)
Synanthropic Rodents3 (5%)
Pets/Free-Roaming 
Cats11 (17%)
Dogs14 (22%)
Other (horses, guinea pigs, rabbits)2 (3%)
Not Specified13 (21%)
a

A total of 62 unique publications were reviewed. The total N for Regions, Health, Outcomes, and Animals is greater than 62 because publications that assessed multiple regions, health outcomes, or animals in their study were counted for each unique region, health outcome, or animal.

Table 2. Summary of Pathogen Characteristics of Studies (n = 62)a Included in Review of Potential Health Impacts from Exposure to Animal Feces
Pathogensn (%)
Bacteria 
Aeromonas hydrophila1 (2%)
Bacteriodales spp.1 (2%)
Campylobacter spp.9 (15%)
Chlamydia trachomatis3 (5%)
Escherichia coli11 (17%)
Klebsiella spp.1 (2%)
Salmonella spp.5 (8%)
Shigella spp.5 (8%)
Vibrio spp.4 (7%)
Yersinia spp.2 (3%)
Helminths 
Ascaridia spp.1 (2%)
Ascaris spp.4 (7%)
Clonorchis spp.1 (2%)
Echinococcus spp.2 (3%)
Enterobius spp.1 (2%)
Hookworm (Ancylostoma spp.)7 (11%)
Hymenolepis spp.1 (2%)
Schistosoma spp.3 (5%)
Spirometra spp.1 (2%)
Strongyloides spp.3 (5%)
Taenia spp.1 (2%)
Toxocara spp.6 (10%)
Trichuris spp.6 (10%)
Microsporidia 
Enterocytozoon bieneusi1 (2%)
Protozoa 
Blastocystis hominis1 (2%)
Cryptosporidium spp.10 (16%)
Cyclospora cayetanensis2 (3%)
Entamoeba spp.6 (10%)
Giardia spp.15 (24%)
Isospora belli2 (3%)
Toxoplasma spp.1 (2%)
Trichomonas hominis1 (2%)
Viruses 
Adenovirus2 (3%)
Astrovirus1 (2%)
Hepatitis E virus1 (2%)
Rotavirus5 (8%)
a

A total of 62 unique publications were reviewed. The total N for all pathogens is greater than 62 because publications that assessed multiple pathogens were counted for each unique pathogen.

Most of the studies we identified for this review were cross-sectional studies (n = 42); other study designs included case-control (n = 3), experimental and quasi-experimental (n = 2), longitudinal (n = 2), cohort (n = 4), and qualitative studies (n = 1). The remaining publications, reported on secondary data analyses (n = 1), a conceptual model (n = 1), or systematic review/meta-analysis (n = 1). Study populations included children, adults, animals, and environmental samples (e.g. stool, blood, water). Most of the studies were conducted in Asia (n = 30), but this review also includes studies conducted in Africa (n = 20), South America (n = 12), and Oceania (n = 1) as well; one literature review included papers from around the globe. Relevant characteristics of the publications included in this review are presented in SI Table S3.

Impact of Exposure to Animals and/or Animal Feces on Human Health

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Most studies assessed exposure to animal feces based on contact with or presence of animals in the environment. Few (n = 9) measured direct human contact with animal feces per se. We illustrate the role of exposure to animal feces and/or contact with or presence of animals and its impact on WASH-related health outcomes in Figure 2. Below we synthesize findings for each of the health outcomes considered, including diarrhea, child growth, EED, pathogen isolation in human stool (bacterial, protozoan, microsporidian, viral), trachoma, and STH infections.

Figure 2

Figure 2. Impact of exposure to animal feces and/or contact with animals to human health.

Diarrhea

Heterogeneous effects of exposure to animals and animal feces on human diarrheal illness were observed among the 18 studies examining diarrhea in this review. A systematic review and meta-analysis found consistent evidence of a positive association between domestic poultry and livestock exposure and diarrheal illness. (5) Animals housed in living quarters increased the risk of diarrhea and/or infection by enteric pathogens in several studies and increased the risk of longer durations of diarrhea. (36-41) Living with chickens infected by zoonotic enteric pathogens increased the risk of diarrhea among children in Lima, Peru. (39)
No associations were found between the presence of animals or animal feces and diarrhea or enteric infection in urban Accra, Ghana and rural Odisha, India. (42, 43) An assessment of Demographic Health Surveys (DHS) from 30 sub-Saharan African countries found an inconsistent relationship across contexts between childhood diarrhea and household livestock ownership; 13 countries indicated livestock ownership as a risk factor but 10 countries exhibited a protective association likely due to confounding with socio-economic status and varied access to improved water and sanitation infrastructure. (26) Cattle ownership in Madagascar was found to be protective against severe diarrhea. (44)

Child Growth

Exposure to fecal pathogens of animal origin may impair child growth, although these effects are not consistently found in the literature (n = 8). For most studies, child growth was measured using anthropometric measurements to calculate standardized age- and sex-specific height-for-age Z-scores (HAZ), weight-for-age Z-scores (WAZ), and weight-for-height Z-scores (WHZ) to classify levels of stunting, being underweight, and wasting, respectfully. In a study in rural Ethiopia, poultry ownership was positively associated with child HAZ, but corralling poultry indoors at night was negatively associated with child HAZ; no association was found between corralling animals indoors at night and child HAZ for other animal species (cattle, goats, sheep, pack animals). (45, 46) Several studies found no association between livestock ownership and child HAZ and WAZ, though livestock diseases might be related to lower child HAZ and WHZ in some groups in rural Kenya. (43, 47) The presence of animal feces in household compounds was negatively associated with child HAZ in rural Bangladesh and Ethiopia. (40)
A recent analysis of agricultural, nutritional, and interview data, along with anthropometric measurements from sub-Saharan Africa, revealed inconsistent evidence for the effects of animal ownership and consumption of animal-sourced foods on child growth. Children in households that consumed animal-sourced foods in Rwanda, Uganda, and Malawi had better anthropometric scores (WHZ and HAZ) than those that did not consume animal-sourced foods; however, children who consumed animal-sourced foods in Ghana and Senegal had lower relative anthropometric scores (WHZ (Ghana only) and HAZ). (46) The analysis of DHS from 30 sub-Saharan African countries similarly found inconsistent results, but data revealed a slight protective effect of the number of animals owned on child stunting. (26)
Child growth effects may be mediated by animal containment and housing practices. Children in households that kept poultry outside the home had significantly better HAZ compared to those in households that kept poultry inside the home in rural Ethiopia. (45) Similarly, in rural Bangladesh the odds of being stunted were higher among children in households with animals corralled in sleeping quarters versus households where animals were not corralled in sleeping quarters. (48)

Environmental Enteric Dysfunction (EED)

Two studies in this review suggest that exposure to animals and animal feces might increase the risk of EED, also referred to as environmental enteropathy, an impairment of intestinal function evident in many young children in low-resource settings that leads to growth faltering and cognitive impairment. (49-54) Children sleeping in households with animal corrals in the sleeping quarters had significantly higher EED scores (calculated from fecal biomarker measurements) than those without animals in the sleeping quarters in rural Bangladesh. (48) Among rural Malawian children, animals sleeping in the same room as the children, combined with use of potentially contaminated water sources and the absence of household pit latrines, was positively associated with EED. (55)

Pathogen Isolation in Human Stool

Several studies examined associations between exposure to animals and/or their feces to subsequent isolation of pathogens in human stool.
Among bacteria, Campylobacter spp. infection was common among children living with domesticated animals, especially poultry, compared to children not living with animals, because children were likely to be in direct contact with chicken feces. (5, 41, 56, 57) A study in peri-urban Peru noted that chickens, dogs, and cats were commonly infected with C. jejuni. (36) Genetic analysis of animal and child stool samples in semirural Ecuador found that C. jejuni sequence types were identical between children and chickens, dogs, guinea pigs, and rabbits; atypical enteropathogenic Escherichia coli (aEPEC) sequence types were identical between children and pigs, dogs, and chickens. (58)
Among protozoal pathogens, Cryptosporidium spp., Giardia spp., and Entamoeba spp. have been associated with exposure to animals. Cryptosporidium spp. identification in child stool was associated with the presence of chickens in the household in Cambodia. (59) In urban Kenya, a study among HIV/AIDS patients found that cryptosporidiosis was associated with contact with animals, (60) and in urban Democratic Republic of the Congo, exposure to farm pigs increased the odds of Cryptosporidium infection among HIV/AIDS patients. (61) Individuals with household pets were 2.6 times more likely to be infected with G. duodenalis assemblage A compared to those without pets in Malaysia. (62) A study of outpatient stool samples from an urban hospital in Yemen found that contact with animals increased the risk of any intestinal protozoan infection (G. duodenalis, E. histolytica, E. dispar) and single infection with Entamoeba spp.; single infection of G. duodenalis was not associated with contact with animals. (63) A study in rural China among individuals with pulmonary tuberculosis found that those raising chickens, ducks, or pigs, and working farmlands barefoot to be significantly associated with protozoan (Blastocystis hominis, Entamoeba spp., Trichomonas hominis) and helminthic infections (hookworm, Trichuris trichiura, Ascaris lumbricoides, Clonorchis sinensis), respectively. (64)
Immunocompromised populations are particularly susceptible to infection by microsporidia, specifically Enterocytozoon bieneusi. A study of microsporidiosis in HIV patients in hospitals in Lima, Peru found that contact with duck or chicken fecal droppings was a risk factor for infection with the E. bieneusi genotype, Peru-1, as were lack of running water, flush toilets, or garbage collection. (65) Among HIV/AIDS patients in Kinshasa, Democratic Republic of the Congo, exposure to farm pigs was associated with higher odds of infection with E. bieneusi or Cryptosporidium spp. (61) In urban India, a study among HIV-positive individuals found that contact with pets and other animals increased the odds of infection with enteric pathogens, including bacterial, protozoan, helminthic, and microsporidian species. (66)
Several studies reported no association between presence of or contact with domestic animals or rodents and their feces and pathogenic infection with certain species of bacteria, (42, 67, 68) protozoans, (59, 63) and viruses. (69)

Trachoma

Exposure to animals and animal feces might increase the risk of trachoma, an infection by the bacterium Chlamydia trachomatis, by potentially providing breeding sites for flies that propagate the infection. The studies in this review do not assess if flies carrying C. trachomatis actually bred on animal feces; the presence of human feces in or near study sites may be a confounding factor. In rural Nigerian households, the presence of animal feces in household compounds was a risk factor for trachomatous inflammation-follicular (TF), a precursor condition to blinding trachoma. (70) In rural Ethiopian households, active trachoma, measured by TF and trachomatous inflammation (TI), was more common in children in families who specifically housed their cattle in their sleeping quarters, though cattle ownership was not associated with trachoma risk. (71) Another study in rural Ethiopia also noted that the presence of animal feces near the house was associated with active trachoma in at least one child in the study households. (72)

Soil-Transmitted Helminth (STH) Infection

Evidence suggests that exposure to animals and animal feces, particularly those of cats and dogs, leads to an increased risk of STH infections. Individuals in urban, low-income households in Brazil were more likely to be diagnosed with hookworm-related cutaneous larva migrans (HrCLM), a parasitic skin disease caused by feline or canine hookworms, if animal feces were present in the compound. (73) Dog owners in Chile and Argentina displayed positive human seropositivity to Echinococcus granulosus and Toxocara canis, respectively. (74, 75) Similarly, the presence of dogs and their feces significantly contributed to children being seropositive for toxocariasis in Sri Lanka. (76) Pregnant women in Bali exposed to oocyst-positive cat feces in their environment were more likely to be serologically positive for Toxoplasma gondii than pregnant women who were not exposed to oocyst-positive cat feces. (77)

Pathways of Exposure to Animal Feces

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The means of characterizing exposure to animals and animal feces varied considerably in the literature we reviewed. Researchers assessed presence of or contact with animals, presence of or contact with animal feces, animal ownership, environmental contamination of public and domestic spaces, and risky husbandry practices (e.g., using cow dung as cooking fuel and slaughtering practices) through structured observations and semistructured interviews. Most publications assessed impacts of raising poultry (chickens, duck, geese, quail) and cattle; studies also assessed impacts of exposure to goats, dogs, sheep, cats, pigs, buffalo, synanthropic rodents (mice, rats), and less commonly, horses, guinea pigs, and rabbits.
We reviewed the literature to identify the extent of human-animal contact with attention to regional, cultural, and urban-rural contextual differences. The evidence of human-animal contact between regional and cultural contexts revealed anecdotal study site-specific information, but did not provide a sufficiently generalizable set of behaviors. The comparative risk of exposure to animal feces in urban compared to rural areas is therefore difficult to determine.
Figure 3 illustrates the pathways for human exposure to zoonotic fecal pathogens using a modified F-diagram. We distinguished transmission pathways dependent on animal species and behaviors versus pathways dependent on human behaviors and practices; the pathways corresponding to human behaviors are independent of the animal species that is the source of the fecal exposure. Below we present the evidence around each of the exposure pathways highlighted in Figure 3; the numbers correspond to the pathways in Figure 3.

Figure 3

Figure 3. Modified F-diagram showing transmission routes of animal feces to humans. Adapted from Wagner, E.; Lanoix, J., Excreta disposal for rural areas and small communities. Monograph Series World Health Organization.1958, 39, 182. Copyright 1958, World Health Organization.

Pathway 1: Contamination of Water Sources

Contamination of both source and stored drinking waters is an important human exposure to animal feces. Several studies demonstrated that open ponds and surface waters are more susceptible to contamination by animal feces, though significant contamination has been observed in public and private tube wells also. (27, 78, 79) In rural India, higher sheep populations in villages increased the odds of detecting higher concentrations of Cryptosporidium spp. in public ponds. (80) Humans sharing water sources with livestock represents a particularly risky behavior in low-income settings. (78, 81-83)

Pathway 2: Contamination of Soil

Many of the pathways for exposure to animal feces occur directly in and around the domestic environment. We found consistent evidence of animals contaminating fields and soil by indiscriminate defecation. Positive associations were found between seropositivity for helminths and soil contaminated by dog and cat feces in households and public settings (e.g., parks, playgrounds). (74, 76) Stray, free-roaming cats and dogs contaminated domestic and public environments with Toxoplasma spp. and helminth eggs in rural and urban communities in LMIC. (29, 30, 84, 85)
Ruminant fecal markers were observed in soil and hand rinse samples from households that did and did not own ruminant species in Bangladesh. (86, 87) Widespread chicken feces contamination has been observed in household kitchens and backyards; (88) chickens might therefore be of particular concern in household environments, because children (up to five years old) have been observed to have contact with chicken feces an average of 2.9 times in a 12 hour span. (57)
Soil was contaminated during the use and disposal of manure on agricultural or residential areas as fertilizer. (83, 89, 90) Manure effluents may also be discharged from cattle storage, potentially contaminating surrounding land. (81)

Pathway 3: Contamination of Food

In the United States and other HIC, where human waste is arguably well-controlled, the burden of enteric disease is largely related to foodborne or animal-associated outbreaks. Most of the important bacterial pathogens of foodborne illness in the United States are transmitted by animals. (91) Even in the case of sophisticated human waste containment, pathogens from poorly managed animal feces can directly contaminate food during the food production process, particularly related to slaughter. As such, foodborne exposure to animal feces in LMIC is likely an important pathway that warrants further research.
Our search, however, uncovered few studies (n = 2) that reported on the contamination of food from animal feces. Campylobacter spp. contamination was found in 34.6% of samples of various types of goat meat collected in the Democratic Republic of Congo. (92) Fresh produce collected from a suburban market in Vietnam was widely contaminated with parasite ova excreted by both humans and animals. (90)

Pathway 4: Contamination via Flies

Flies, potential vectors of fecal contamination, may be associated with negative health outcomes. Three studies specifically examined flies as vectors for trachoma infection (70, 72) and diarrheal illness. (38) In rural Ethiopia and Nigeria, the presence of flies in the home (due to presence of cows, waste disposed near the home, and defecation near the home) (72) and on the face (70) was positively associated with trachoma. In rural India, higher fly densities were associated with longer durations of diarrhea. (38) Also, the absence of animals in or near the home was protective against high fly densities. An additional study in rural Indian households assessing the presence of cowsheds and the presence of flies noted that fly counts were higher in households owning cowsheds versus those without cowsheds. (43)

Pathway 5: Contamination of Human Hands

Cohabitation of animals and humans is a common practice in LMIC and is one of the primary risk factors we identified in this review. Though most studies did not explicitly observe human-to-animal contact, we used animal ownership and the presence of animals in and around households as a proxy for direct contact with animals, a pathway important for exposure to animal feces. In many domestic settings, livestock, including cattle and poultry, were housed in the family’s sleeping quarters, (45, 48, 63, 89) increasing the potential for contamination in the household environment. Households kept livestock in sleeping quarters at night to protect them from thieves or from being hunted by other animals. (89) Poultry were generally allowed to scavenge for food inside and outside living quarters in rural villages in Bangladesh. (89) Household members directly contacted animal feces when handling manure, sometimes handling cow manure from E. coli-positive and negative herds with bare hands. (81, 83, 93)
Multiple studies in rural and urban settings found positive associations between high levels of contact with animals and/or animal feces and negative health outcomes. (33, 62, 69, 74, 94, 95) The presence of animal feces in household compounds has been associated with diarrhea, lower HAZ, and HrCLM. (37, 40, 73) Contact with manure has also been associated with the presence of antibodies to C. jejuni and pathogenic E. coli. (28)

Pathway 6: Contamination of Fomites

Other sources of direct or indirect contamination by animal feces include fomites, such as cooking and infant feeding utensils and toys. Two studies in South Asia evaluated environmental fecal contamination in rural households using toys which may be more likely to come into direct contact with animal feces as they are used for play. In rural India, the average fecal contamination of toys increased as the number of animal fecal piles observed in the household or within the compound increased. (96) The authors suggest that the fecal contamination detected on the toys is likely from both human and animal feces. In rural Bangladesh, fewer toys were contaminated with E. coli (used as a fecal indicator bacteria) in households in villages with more than 50% latrine coverage, no open defecation, handwashing facilities with soap, protected source water in dwellings, safe disposal of child feces, and no animals present in the household but used plaster floors with cow dung. (97) In this study, the households’ substantial WASH infrastructure used to limit human fecal contamination likely played a role in minimizing fecal contamination in the household, but the absence of animals is also noteworthy. Interestingly, the study noted that households with floors of soil or mud surfaces in the living and entrance areas had statistically lower amounts of bacteria on toys compared to households with cement floors, but there was no difference in contamination levels of the toys between households that plastered with cow dung versus households that did not plaster with cow dung. (97)
Two studies in this review examined fecal contamination on cooking and feeding utensils. In a peri-urban community in Lima, Peru, a study of environmental contamination of household objects, including infant bottle nipples, feeding bottles, spoons, and can openers, found that 35% of the objects (n = 80) were positive for E. coli cultures. (36) Another household-level study found that infants’ cups and spoons yielded E. coli cultures in 23% of households (n = 5). (88) In these studies, indirect contamination of fomites likely occurred when the fomites dropped onto contaminated floors or were handled by contaminated fingers; direct exposures of fomites to animal feces were not addressed in these studies. (36, 88)

Interventions Limiting Exposure to Animal Feces

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We adapted the traditional F-diagram to show pathways of human exposure to animal feces and assessed potential interventions along those pathways (Figure 4). While “secondary” barriers to block transmission of animal feces to humans are capable of controlling both human and animal feces, “primary” barriers are specific to controlling exposure to animal feces. These primary barriers have largely not been considered in traditional WASH interventions designed to limit exposure to human feces, and few studies have evaluated their potential in reducing the burden of animal feces on human health. Our review uncovered only seven intervention studies specifically aimed at controlling this primary barrier of exposure to animal feces. The control measures that have been evaluated and/or suggested as potential interventions in the studies included in this review are described below; Table 3 summarizes these intervention studies.

Figure 4

Figure 4. Modified F-diagram including interventions that can block human exposure to animal feces. Adapted from Wagner, E.; Lanoix, J., Excreta disposal for rural areas and small communities. Monograph Series World Health Organization.1958, 39, 182. Copyright 1958, World Health Organization.

Table 3. Summary of Trials Evaluating Potential Interventions Limiting Exposure to Animal Feces
interventioninterrupted fecal-oral pathwayreferencedescription of interventionstudy contexteffectiveness of intervention
separating chickens from human living quartersfeces → fluids, food, fingersHarvey et al. (2003)provided wooden corrals with commercial fish netting walls and fiberglass roofsperi-urban Peruuptake was low among households that did not corral their poultry before the study
 separated poultry by age, sex, and/or species corralling did not eliminate child exposure to poultry
Oberhelman et al. (2006)provided corrals sized based on number of chickens in household and the size of available areas on the property outside living quartersperi-urban Peruchicken feces from corralled chickens was colonized with Campylobacter spp. more often than control group
     corralling might have increased the risk of campylobacteriosis in children
 
providing animal feces scoopsfeces → fluids, fields, fingersBoehm et al. (2016)provided metal scoops for removal of animal feces and safe disposal in a dual-pit latrinerural Bangladeshruminant fecal markers detected more often in stored water of control vs sanitation compounds
 provided concrete ring-based dual-pit latrines with slabs, water seals, and superstructures impossible to disentangle effects of provision of metal scoop from other components
 provided ″potties″ for young children  
Hussain (2013)provided “sani-scoops” for disposal of child and animal fecesrural Bangladeshreported use of the hardware was relatively high
   provide “potties” for young children minimal differences detected in the presence of human and animal feces in compounds between baseline and follow-up visits
 
creating safe child play spacesfeces → fingers; fields → humanSHINE Trial et al. (2015)provided safe play areas among a package of other WASH interventionsrural Zimbabweongoing trial; results not yet published
 
improving animal veterinary careanimal → fecesHall et al. (2012)increased veterinary care of dairy cattlerural Bangladeshincreased access to health services, human and veterinary, in most villages reduces exposure to emerging infectious disease hazards, as well as removing livestock from one in three households, improving manure management in all villages, and improving water and latrines in all villages
   encouraged behavior change to reduce exposure to manure  
   improved agricultural production  

Separating Chickens from Human Living Quarters

Cohabitation with animals has been associated with negative health outcomes. Animal containment practices can reduce human exposure to animal feces contamination in domestic environments. However, according to two studies that evaluated the effects of separating chickens from human living quarters in peri-urban areas of Lima, Peru, corralling chickens did not eliminate child exposure to poultry; it might actually increase the risk of campylobacteriosis potentially due to continued exposure to chickens and/or from increased concentrations of Campylobacter spp. in the corralling area. (41, 98) Harvey et al. evaluated an intervention to contain poultry in wooden corrals with commercial fish netting walls and fiberglass roofs, in addition to separating poultry by age, sex, and/or species. (98) Households that used corrals most of the time before the study consistently used the experimental corrals from the start; households who let their poultry roam before the study intervention housed their poultry in corrals less consistently. Despite efforts to separate children from poultry, some children were still exposed because they helped catch poultry and move them into the corral, climbed on corral walls and doors, poked fingers through the netting, entered corrals to play with the poultry, or helped with daily animal care. In another area of peri-urban Lima, researchers installed chicken corrals in intervention households. (41) They found that chicken feces from the control group were colonized with Campylobacter spp. more often than that from the corral group, but both groups were heavily colonized (63.9% and 58.1% of chicken stool samples, respectively). The rate of diarrhea in children was higher in the corral group (2.79 episodes per person per year [epy]) than the group without corrals (2.07 epy; p = 0.017), suggesting that chicken corralling may have increased the risk of Campylobacter-related diarrhea in children from children entering and handling the chickens in the corrals and/or encouraged the children to interact with the chickens due to close proximity of the corrals to the home. In addition, the corrals concentrated chicken feces in a single area that could have contributed to an increased concentration of Campylobacter spp. in the area.

Providing Animal Feces Scoops

Similar to animal containment practices, promotion of animal waste removal from the domestic environment and proper disposal could disrupt the contamination of environmental reservoirs by animal feces. Though sanitation interventions have primarily focused on containing human feces by providing improved latrines, some studies have added components to encourage the safe disposal of animal feces as well. The WASH Benefits trial provided a metal scoop to households for removal of animal feces from the environment and safe disposal in a dual-pit latrine as part of a sanitation intervention in rural Bangladesh. (99) The authors hypothesize that the use of the metal scoops might remove animal feces from sanitation compounds, but might ultimately contaminate the community’s water source downstream of the disposed animal feces. While the intervention group had lower ruminant fecal markers, the scoop was coupled with provision of a household dual-pit latrine as well as potties for young children, so disaggregating the impact of animal feces disposal was not feasible. (86)
In rural Bangladesh, households were provided potties and “sani-scoops”, hoe-like tools for disposal of child and animal feces. Although reported use of the hardware was relatively high, minimal differences were detected between the presence of human and animal feces in compounds at baseline and follow-up visits. (100) Interviews with study participants revealed that liquid feces was hard to remove from uneven or hard surfaces with the sani-scoop, and animal feces was not generally perceived as “disgusting”. Additionally, household members were unlikely to change their habits of sweeping and cleaning courtyards of feces only at certain times during the day, potentially exposing them to fecal contamination at other times of day. (100) To reduce exposure to animal feces, education regarding safe animal feces disposal methods might be necessary as a complement to provision of sanitary scoops designed to remove animal feces.

Reducing Contamination of Environmental Sources by Controlling Animal Movement

Soil is oftentimes a reservoir for animal feces contamination in both public and domestic areas, and animal containment measures may reduce animal fecal contamination. In urban Brazil, fencing around public sandboxes was a significant protective factor against soil contamination of helminths from dog feces because the fences prevented stray dogs from accessing the area. (84)

Creating Safe Child Spaces

Rather than corralling animals, protective and hygienic barriers may prevent humans, specifically children, from coming into contact with animal feces. Since there are constant opportunities for young children to put contaminated fingers in their mouths or ingest feces-contaminated soil, creating spaces for children separate from livestock could reduce exposure to animal feces. The Sanitation, Hygiene, and Infant Nutrition Efficacy (SHINE) trial in Zimbabwe is testing this approach by providing households with safe play areas for children in addition to a package of other water and sanitation interventions. (101) The trial is ongoing, and results have not yet been published.

Improving Animal Veterinary Care

Veterinary care may reduce the spread of zoonotic fecal pathogens from livestock and domestic animals by reducing pathogen carriage in animals. In Bangladesh, exposure to emerging infectious disease hazards were significantly reduced by removing livestock from one in three households, improving manure management in all villages, improving water and latrines in all villages, and increasing access to health services–human and veterinary–in most villages. (102) The intervention also increased income from animal agriculture.

Promoting Handwashing and Domestic Environment Hygiene

Handwashing and domestic hygiene have been recommended by several studies finding positive associations between animal exposure, raw vegetable consumption, geophagy, or lack of handwashing before meals and zoonotic pathogenic infection. (36, 56, 62, 74, 103) Unlike the animal feces “sanitation” interventions, handwashing and domestic hygiene are designed to protect humans from exposure to both animal and human feces. Lack of handwashing might be a generalizable and important behavior to target; another study found that handwashing by mothers was infrequent and children placed their hands in their mouths 38 times in 130 h on average. (88) However, we did not find any studies that explicitly examined the effects of handwashing after contact with animals.

Limitations

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We included all studies that meet the inclusion criteria regardless of methodological rigor. A majority of the publications are cross-sectional studies, making it difficult to assess the causal attribution of exposure to animal feces on human health. Due to the lack of in-home observations, most studies we reviewed used surveys and interviews assessing animal ownership or contact with animals as proxies for exposure to animal feces. Such exposure measures might be poor indicators of true exposure to animal feces, and in fact, could measure behaviors associated with potential health benefits to households. For example, a study in rural Ethiopia carefully looked at the benefits of poultry ownership on egg consumption versus the risks posed by corralling poultry inside the home, (45) but few studies empirically address these competing risks and benefits. There is also limited research on specific exposure pathways to animal feces and important confounding variables are not well understood or quantified. Due to the use of household interviews, studies were subject to recall bias when participants were asked to self-report past bouts of diarrhea. The use of convenience sampling methods, instead of random sampling methods, may have led to selection bias. Many of the studies included in this review had small sample sizes, thus preventing them from achieving sufficient power to detect many of the health outcomes examined in this review.

Future Research

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Our review highlights the scarcity of information available on the human health impacts of exposure to poorly managed animal feces transmitted via WASH-related pathways. To accurately capture human exposure to animal feces, future research could prioritize longitudinal studies with in-home observation methodologies. In addition, data to inform a rigorous assessment of the contribution of poorly managed animal feces to the global burden of disease is not available. Yet many associations between some measure of animal or animal feces exposure and health effects have been explored, and interventions designed to control human fecal waste will likely lead to suboptimal health gains in the absence of efforts to control animal feces in the same environment. Understanding the true burden of disease from poorly managed animal feces given the current infrastructure and behavioral contexts would provide important guidance for policy and programs.
It would be of considerable value to categorize and measure exposure to animal feces and to develop and evaluate interventions to mitigate that risk. Using direct observations and interviews/discussion with domestic animal owners, household members including women and children, veterinarians, and community leaders, more data are needed to
  • understand the key behaviors and contexts associated with exposure to animal feces;

  • identify key points (“hot spots”) of human contact with animals and/or their feces in different contexts (e.g., domestic, community);

  • understand the factors associated with direct contamination of food from poorly managed animal feces, particularly in food markets and noncommercial agricultural/meat production facilities; and

  • identify cultural behaviors that influence animal husbandry and animal feces management practices.

Understanding the various pathways and behaviors that expose humans to animal feces could allow researchers develop innovative interventions limiting such exposures in LMIC. Behavioral approaches to WASH should be evaluated further to understand their potential for controlling human exposure to animal feces. Our review demonstrates that many people did not feel disgust toward animal feces (100) and exposure to poorly managed animal feces might occur at the community-level rather than just the household-level. An evaluation of a community-led total sanitation (CLTS) program in rural Mali found that households that participated in the CLTS program were less likely to have observable animal feces in their compound courtyard; (20) CLTS programs integrating animal feces management could therefore be considered as potential control measures. Interventions executed in HIC, such as building bridges across streams to reduce point source contamination of waterways by livestock, could be also adapted for LMIC. (104)
Once the various pathways of human exposure to animal feces are explored and understood, it would be possible to calculate specific health risks associated with exposure to animal feces, including both acute infectious diseases and chronic sequelae, such as EED and growth faltering, by conducting intervention trials. These intervention trials can measure before-and-after health outcomes among study populations who are provided interventions to limit or eliminate exposure to animal feces across multiple pathways compared to health outcomes in similar study populations who are not provided interventions to limit or eliminate exposure to animal feces. In addition to understanding the human behaviors and possible health outcomes associated with exposure to animal feces, future laboratory and field-based research must also consider pathogen biology by
  • quantifying the concentration and shedding rates of pathogens in the feces of animal hosts and understanding the factors that determine variability in these parameters;

  • quantifying die-off rates of pathogens outside of animal hosts and the factors that determine them;

  • understanding the factors controlling the fate and transport processes of pathogens outside of the animal host, under varying environmental conditions; and

  • understanding how antibiotic usage in humans and animals may be contributing to antibiotic resistance of zoonotic pathogens.

These types of data will be critical for parametrizing quantitative microbial risk assessment models and transmission models that can provide important insights on zoonotic transmission of pathogens from animal feces to humans. Studies could also take advantage of new molecular techniques that provide insights into transmission processes, such as microbial source tracking, (105) strain typing, multiplex enteropathogen assays, (106, 107) and metagenomics. (108)
In addition, work is needed to understand the role of exposure to animal feces on negative human health outcomes in various rural, urban, and peri-urban contexts, from human host and pathogen biology to overarching public policy. This is illustrated in Figure 5, a diagram showing priority research gaps in assessing the role of contact with animal feces on human health, which we adapted from the socio-ecological model. (109) The potential for acute and chronic human health impacts to manifest from exposure to animal feces is dependent on biology within the human host (i.e., intestinal microbiome), including age- and sex-dependent susceptibilities to different zoonotic fecal pathogens and potential immunities developed from low-level exposures to animals and their feces. To understand the health risks associated with exposure to animal feces, it is crucial to understand the microbiology of pathogens found in animal feces, including their shedding and die-off rates and their transport processes. Human behaviors and practices are additional vital elements to assessing human health outcomes from exposure to animal feces. At the individual level, it is important to understand knowledge around risks and preventions of exposure to animal feces. In LMIC, gender and age divisions in responsibility for care, decisions, and the control of livestock production are common. (93, 110) Gender and age divisions in labor should be explored further to understand how these variables influence risk of exposure to animal feces. Future research could characterize human behaviors in the household that result in exposure to animal feces, such as animal housing and containment practices or animal feces management. Our review points to the probable importance of community-level animal feces contamination on the human health burden, particularly in regards to food contamination in markets, soil contamination in the public environment from free-roaming animals, and contamination of community water sources; as such future research should investigate traditional husbandry practices in different regions and contexts. At the policy level, it would be valuable to monitor and evaluate the effect of national policies and regulations aimed at promoting animal health (e.g., immunization, feed standards), veterinary care (e.g., neutering/spaying policies), and safe management of animal manure and feces.

Figure 5

Figure 5. Priority research gaps in assessing human health impacts from exposure to poorly managed animal feces. This figure, an adaption from the socio-ecological model, represents how the “spheres of influence,” from human host and zoonotic pathogen biology to national policies, influence the health of the human host. Example items for future research within each sphere are provided.

One particularly interesting line of inquiry would be to evaluate the trade-off between the nutritional benefits of livestock ownership with the health risks associated with exposure to animals. Many development projects promote animal husbandry as a way to improve nutrition and livelihoods, yet this review highlights the ways that contact between animal feces and humans may potentially be deleterious to health, especially in children. This trade-off was highlighted by several of the articles in this review. (26, 44) Once more information is available on the magnitude of the health risk posed by animal feces exposure, knowledge around animal feces management, and key points of contact between humans and animals, culturally appropriate intervention strategies can be developed and rigorously evaluated.

Conclusions

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As envisioned by the Sustainable Development Goals, the world will achieve universal access to safe water, coverage of safely managed sanitation, and handwashing with soap by 2030. (111) However, even if these ambitious targets are met, effectively eliminating direct and indirect exposure to human feces, risks associated with exposure to animal feces will remain. The literature in this review suggests that exposure to animals and animal feces has mixed effects on diarrhea and child growth, potentially increases risks of EED, STH infection, and trachoma, and has mixed effects on isolation of zoonotic pathogens in human stool. There is some evidence for the WASH-related pathways by which humans are exposed to animals and animal feces, but more research on pathogen transmission parameters, animal husbandry practices, and cultural/social influences is warranted. Furthermore, few studies have tested interventions that control the transmission of pathogens in animal feces and limit human exposure to animal feces. As we increasingly understand the contribution of poorly managed animal feces to the overall global burden of disease, it is important to gain insights into the routes by which humans are exposed to animal feces to design efforts to interrupt these pathways and reduce subsequent human health impacts.

Supporting Information

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The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acs.est.7b02811.

  • Further details about methods including full search string and databases used, global PRISMA chart, data extraction form, PRISMA checklist, and table of study characteristics (PDF)

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Most electronic Supporting Information files are available without a subscription to ACS Web Editions. Such files may be downloaded by article for research use (if there is a public use license linked to the relevant article, that license may permit other uses). Permission may be obtained from ACS for other uses through requests via the RightsLink permission system: http://pubs.acs.org/page/copyright/permissions.html.

Author Information

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  • Corresponding Author
  • Authors
    • Gauthami Penakalapati - Department of Environmental Health, Emory University, Atlanta, Georgia 30322 United StatesOrcidhttp://orcid.org/0000-0003-2119-7431
    • Jenna Swarthout - Department of Environmental Health, Emory University, Atlanta, Georgia 30322 United States
    • Miranda J. Delahoy - Department of Environmental Health, Emory University, Atlanta, Georgia 30322 United States
    • Lydia McAliley - Department of Environmental Health, Emory University, Atlanta, Georgia 30322 United States
    • Breanna Wodnik - Department of Environmental Health, Emory University, Atlanta, Georgia 30322 United States
    • Karen Levy - Department of Environmental Health, Emory University, Atlanta, Georgia 30322 United States
  • Notes
    The authors declare no competing financial interest.

Acknowledgment

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This work was supported by the Bill & Melinda Gates Foundation (grant OPP1157522 to Emory University). K.L. is supported by the National Institute for Allergy and Infectious Diseases, NIH (grant 1K01AI103544). The content is solely the responsibility of the authors and does not necessarily represent the official views of the funders.

References

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This article references 111 other publications.

  1. 1
    Jones, K. E.; Patel, N. G.; Levy, M. A.; Storeygard, A.; Balk, D.; Gittleman, J. L.; Daszak, P. Global trends in emerging infectious diseases Nature 2008, 451 (7181) 990 993 DOI: 10.1038/nature06536
  2. 2
    World Health Organization. The Control of Neglected Zoonotic Diseases: A Route to Poverty Alleviation: Report of a Joint WHO/DFID-AHP Meeting; WHO: Geneva, Switzerland, 2006.
  3. 3
    Wagner, E.; Lanoix, J. Excreta disposal for rural areas and small communities Monogr Ser. World Health Org. 1958, 39, 182
  4. 4
    Food and Agricultural Organization FAOSTAT. http://www.fao.org/faostat/en/#home (accessed 7 February 2017) .
  5. 5
    Zambrano, L. D.; Levy, K.; Menezes, N. P.; Freeman, M. C. Human diarrhea infections associated with domestic animal husbandry: a systematic review and meta-analysis Trans. R. Soc. Trop. Med. Hyg. 2014, 108 (6) 313 325 DOI: 10.1093/trstmh/tru056
  6. 6
    Batz, M. B.; Henke, E.; Kowalcyk, B. Long-term consequences of foodborne infections Infectious disease clinics of North America. 2013, 27 (3) 599 616 DOI: 10.1016/j.idc.2013.05.003
  7. 7
    Moore, S. R.; Lima, N. L.; Soares, A. M.; Oriá, R. B.; Pinkerton, R. C.; Barrett, L. J.; Guerrant, R. L.; Lima, A. A. Prolonged episodes of acute diarrhea reduce growth and increase risk of persistent diarrhea in children Gastroenterology 2010, 139 (4) 1156 1164 DOI: 10.1053/j.gastro.2010.05.076
  8. 8
    Lorntz, B.; Soares, A. M.; Moore, S. R.; Pinkerton, R.; Gansneder, B.; Bovbjerg, V. E.; Guyatt, H.; Lima, A. M.; Guerrant, R. L. Early childhood diarrhea predicts impaired school performance Pediatric infectious disease journal 2006, 25 (6) 513 520 DOI: 10.1097/01.inf.0000219524.64448.90
  9. 9
    Robert-Gangneux, F.; Dardé, M.-L. Epidemiology of and diagnostic strategies for toxoplasmosis Clin. Microbiol. Rev. 2012, 25 (2) 264 296 DOI: 10.1128/CMR.05013-11
  10. 10
    Wang, H.; Naghavi, M.; Allen, C.; Barber, R. M.; Bhutta, Z. A.; Carter, A.; Casey, D. C.; Charlson, F. J.; Chen, A. Z.; Coates, M. M.; al, e. Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death: a systematic analysis for the Global Burden of Disease Study Lancet. 2015, 388 (10053) 1459 1544
  11. 11
    Kotloff, K. L.; Nataro, J. P.; Blackwelder, W. C.; Nasrin, D.; Farag, T. H.; Panchalingam, S.; Wu, Y.; Sow, S. O.; Sur, D.; Breiman, R. F.; Faruque, A. S. G.; Zaidi, A. K. M.; Saha, D.; Alonso, P. L.; Tamboura, B.; Sanogo, D.; Onwuchekwa, U.; Manna, B.; Ramamurthy, T.; Kanungo, S.; Ochieng, J. B.; Omore, R.; Oundo, J. O.; Hossain, A.; Das, S. K.; Ahmed, S.; Qureshi, S.; Quadri, F.; Adegbola, R. A.; Antonio, M.; Hossain, M. J.; Akinsola, A.; Mandomando, I.; Nhampossa, T.; Acácio, S.; Biswas, K.; O’Reilly, C. E.; Mintz, E. D.; Berkeley, L. Y.; Muhsen, K.; Sommerfelt, H.; Robins-Browne, R. M.; Levine, M. M. Burden and aetiology of diarrhoeal disease in infants and young children in developing countries (the Global Enteric Multicenter Study, GEMS): a prospective, case-control study Lancet 2013, 382 (9888) 209 222 DOI: 10.1016/S0140-6736(13)60844-2
  12. 12
    Dufour, A.; Bartram, J.; Bos, R.; Gannon, V. Animal Waste, Water Quality and Human Health; IWA Publishing: London, UK, 2012, 6 130.
  13. 13
    Clasen, T. F.; Bostoen, K.; Schmidt, W.-P.; Boisson, S.; Fung, I. C. H.; Jenkins, M. W.; Scott, B.; Sugden, S.; Cairncross, S., Interventions to improve disposal of human excreta for preventing diarrhoea. Cochrane Database of Systematic Reviews 2010, (6). doi:  DOI: 10.1002/14651858.CD007180.pub2 .
  14. 14
    Stocks, M. E.; Ogden, S.; Haddad, D.; Addiss, D. G.; McGuire, C.; Freeman, M. C. Effect of Water, Sanitation, and Hygiene on the Prevention of Trachoma: A Systematic Review and Meta-Analysis PLoS Medicine. 2014, 11 (2) e1001605 DOI: 10.1371/journal.pmed.1001605
  15. 15
    Strunz, E. C.; Addiss, D. G.; Stocks, M. E.; Ogden, S.; Utzinger, J.; Freeman, M. C. Water, Sanitation, Hygiene, and Soil-Transmitted Helminth Infection: A Systematic Review and Meta-Analysis PLoS Medicine. 2014, 11 (3) e1001620 DOI: 10.1371/journal.pmed.1001620
  16. 16
    Barreto, M. L.; Genser, B.; Strina, A.; Assis, A. M. O.; Rego, R. F.; Teles, C. A.; Prado, M. S.; Matos, S. M. A.; Santos, D. N.; dos Santos, L. A.; Cairncross, S.; Teixeira, M. G. Effect of city-wide sanitation programme on reduction in rate of childhood diarrhoea in northeast Brazil: assessment by two cohort studies Lancet 2007, 370 (9599) 1622 1628 DOI: 10.1016/S0140-6736(07)61638-9
  17. 17
    Clasen, T.; Boisson, S.; Routray, P.; Torondel, B.; Bell, M.; Cumming, O.; Ensink, J.; Freeman, M.; Jenkins, M.; Odagiri, M.; Ray, S.; Sinha, A.; Suar, M.; Schmidt, W.-P. Effectiveness of a rural sanitation programme on diarrhoea, soil-transmitted helminth infection, and child malnutrition in Odisha, India: a cluster-randomised trial Lancet Global Health 2014, 2 (11) e645 e653 DOI: 10.1016/S2214-109X(14)70307-9
  18. 18
    Emerson, P. M.; Lindsay, S. W.; Alexander, N.; Bah, M.; Dibba, S.-M.; Faal, H. B.; Lowe, K.; McAdam, K. P. W. J.; Ratcliffe, A. A.; Walraven, G. E. L.; Bailey, R. L. Role of flies and provision of latrines in trachoma control: cluster-randomised controlled trial Lancet 2004, 363 (9415) 1093 1098 DOI: 10.1016/S0140-6736(04)15891-1
  19. 19
    Patil, S. R.; Arnold, B. F.; Salvatore, A. L.; Briceno, B.; Ganguly, S.; Colford, J. M., Jr.; Gertler, P. J. The Effect of India’s Total Sanitation Campaign on Defecation Behaviors and Child Health in Rural Madhya Pradesh: A Cluster Randomized Controlled Trial PLOS Medicine. 2014, 11 (8) e1001709 DOI: 10.1371/journal.pmed.1001709
  20. 20
    Pickering, A. J.; Djebbari, H.; Lopez, C.; Coulibaly, M.; Alzua, M. L. Effect of a community-led sanitation intervention on child diarrhoea and child growth in rural Mali: a cluster-randomised controlled trial Lancet Global Health 2015, 3 (11) e701 e711 DOI: 10.1016/S2214-109X(15)00144-8
  21. 21
    Gyorkos, T. W.; Maheu-Giroux, M.; Blouin, B.; Casapia, M. Impact of Health Education on Soil-Transmitted Helminth Infections in Schoolchildren of the Peruvian Amazon: A Cluster-Randomized Controlled Trial PLoS Neglected Trop. Dis. 2013, 7 (9) e2397 DOI: 10.1371/journal.pntd.0002397
  22. 22
    West, S.; Muñoz, B.; Lynch, M.; Kayongoya, A.; Chilangwa, Z.; Mmbaga, B. B. O.; Taylor, H. R. Impact of face-washing on trachoma in Kongwa, Tanzania Lancet 1995, 345 (8943) 155 158 DOI: 10.1016/S0140-6736(95)90167-1
  23. 23
    Freeman, M. C.; Clasen, T.; Brooker, S. J.; Akoko, D. O.; Rheingans, R. The Impact of a School-Based Hygiene, Water Quality and Sanitation Intervention on Soil-Transmitted Helminth Reinfection: A Cluster-Randomized Trial Am. J. Trop. Med. Hyg. 2013, 89 (5) 875 883 DOI: 10.4269/ajtmh.13-0237
  24. 24
    Colford, J. M. J.; Luby, S. P.; Null, C.; Stewart, C. P. In The WASH Benefits Study: Cluster-Randomized Trials in Bangladesh and Kenya to Measure the Effects of Individual and Combined Water Quality, Sanitation, Handwashing and Nutrition Interventions on Child Growth and Diarrhea ASTHM, Atlanta, GA, 2016; Atlanta, GA, 2016.
  25. 25
    Garn, J. V.; Sclar, G. D.; Freeman, M. C.; Penakalapati, G.; Alexander, K. T.; Brooks, P.; Rehfuess, E. A.; Boisson, S.; Medlicott, K. O.; Clasen, T. F. The impact of sanitation interventions on latrine coverage and latrine use: A systematic review and meta-analysis Int. J. Hyg. Environ. Health 2017, 220 (2, Part B) 329 340 DOI: 10.1016/j.ijheh.2016.10.001
  26. 26
    Kaur, M.; Graham, J.; Eisenberg, J. N. S. Livestock Ownership among Rural Households and Child Morbidity and Mortality: An Analysis of Demographic Health Survey Data from 30 Sub-Saharan African Countries (2005–2015) Am. J. Trop. Med. Hyg. 2017, 96 (3) 741 748 DOI: 10.4269/ajtmh.16-0664
  27. 27
    Odagiri, M.; Schriewer, A.; Daniels, M. E.; Wuertz, S.; Smith, W. A.; Clasen, T.; Schmidt, W.-P.; Jin, Y.; Torondel, B.; Misra, P. R.; Panigrahi, P.; Jenkins, M. W. Human fecal and pathogen exposure pathways in rural Indian villages and the effect of increased latrine coverage Water Res. 2016, 100, 232 244 DOI: 10.1016/j.watres.2016.05.015
  28. 28
    Belongia, E. A.; Chyou, P. H.; Greenlee, R. T.; Perez-Perez, G.; Bibb, W. F.; DeVries, E. O. Diarrhea Incidence and Farm-Related Risk Factors for Escherichia coli O157:H7 and Campylobacter jejuni Antibodies among Rural Children J. Infect. Dis. 2003, 187 (9) 1460 1468 DOI: 10.1086/374622
  29. 29
    Cinquepalmi, V.; Monno, R.; Fumarola, L.; Ventrella, G.; Calia, C.; Greco, M. F.; de Vito, D.; Soleo, L. Environmental Contamination by Dog’s Faeces: A Public Health Problem? Int. J. Environ. Res. Public Health 2013, 10 (1) 72 DOI: 10.3390/ijerph10010072
  30. 30
    Jung, B. K.; Lee, S. E.; Lim, H.; Cho, J.; Kim, D. G.; Song, H.; Kim, M. J.; Shin, E. H.; Chai, J. Y. Toxoplasma gondii B1 gene detection in feces of stray cats around Seoul, Korea and genotype analysis of two laboratory-passaged isolates Korean J. Parasitol. 2015, 53 (3) 259 263 DOI: 10.3347/kjp.2015.53.3.259
  31. 31
    Tobin, M. R.; Goldshear, J. L.; Price, L. B.; Graham, J. P.; Leibler, J. H. A Framework to Reduce Infectious Disease Risk from Urban Poultry in the United States Public Health Rep. 2015, 130 (4) 380 391 DOI: 10.1177/003335491513000417
  32. 32
    Williams, S.; Patel, M.; Markey, P.; Muller, R.; Benedict, S.; Ross, I.; Heuzenroeder, M.; Davos, D.; Cameron, S.; Krause, V. Salmonella in the tropical household environment - Everyday, everywhere J. Infect. 2015, 71 (6) 642 648 DOI: 10.1016/j.jinf.2015.09.011
  33. 33
    Williams, S.; Markey, P.; Harlock, M.; Binns, P.; Gaggin, J.; Patel, M. Individual and household-level risk factors for sporadic salmonellosis in children J. Infect. 2016, 72 (1) 36 44 DOI: 10.1016/j.jinf.2015.09.014
  34. 34
    Headey, D.Newsflash: Chickens don’t use toilets - Why global WASH efforst should start focusing on animal feces. http://www.ifpri.org/blog/newsflash-chickens-dont-use-toilets (accessed 7 February 2017) .
  35. 35
    Moher, D.; Liberati, A.; Tetzlaff, J.; Altman, D. G. The, P. G., Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement PLOS Medicine. 2009, 6 (7) e1000097 DOI: 10.1371/journal.pmed.1000097
  36. 36
    Black, R. E.; Lopez de Romaña, G.; Brown, K. H.; Bravo, N.; Bazalar, O. G.; Kanashiro, H. C. Incidence and etiology of infantile diarrhea and major routes of transmission in Huascar, Peru Am. J. Epidemiol. 1989, 129 (4) 785 799 DOI: 10.1093/oxfordjournals.aje.a115193
  37. 37
    Bukenya, G. B.; Nwokolo, N. Compound hygiene, presence of standpipe and the risk of childhood diarrhoea in an urban settlement of Papua New Guinea International Journal of Epidemiology 1991, 20 (2) 534 539 DOI: 10.1093/ije/20.2.534
  38. 38
    Collinet-Adler, S.; Babji, S.; Sarkar, R.; Kattula, D.; Mohan, V.; Ward, H.; Kang, G.; Balraj, V.; Naumova, E. Environmental indicators of diarrhea in Vellore, India Am. J. Trop. Med. Hyg. 2011, 85 (6) 175
  39. 39
    Grados, O.; Bravo, N.; Black, R. E.; Butzler, J. P. Paediatric campylobacter diarrhoea from household exposure to live chickens in Lima, Peru Bull. World Health Org. 1988, 66 (3) 369 374
  40. 40
    Headey, D.; Nguyen, P.; Kim, S.; Rawat, R.; Ruel, M.; Menon, P. Is Exposure to Animal Feces Harmful to Child Nutrition and Health Outcomes? A Multicountry Observational Analysis Am. J. Trop. Med. Hyg. 2017, 96 (4) 961 969 DOI: 10.4269/ajtmh.16-0270
  41. 41
    Oberhelman, R. A.; Gilman, R. H.; Sheen, P.; Cordova, J.; Zimic, M.; Cabrera, L.; Meza, R.; Perez, J. An Intervention-Control Study of Corraling of Free-Ranging Chickens to Control Campylobacter Infections Among Children in a Peruvian Periurban Shantytown Am. J. Trop. Med. Hyg. 2006, 74 (6) 6
  42. 42
    Adjei, A. A.; Armah, H.; Rodrigues, O.; Renner, L.; Borketey, P.; Ayeh-Kumi, P.; Adiku, T.; Sifah, E.; Lartey, M. Cryptosporidium spp., a frequent cause of diarrhea among children at the Korle-Bu Teaching Hospital, Accra, Ghana Jpn. J. Infect. Dis. 2004, 57 (5) 216 219
  43. 43
    Schmidt, W. P.; Boisson, S.; Routray, P.; Bell, M.; Cameron, M.; Torondel, B.; Clasen, T. Exposure to cows is not associated with diarrhoea or impaired child growth in rural Odisha, India: a cohort study Epidemiol. Infect. 2016, 144 (1) 53 63 DOI: 10.1017/S0950268815001090
  44. 44
    Randremanana, R. V.; Razafindratsimandresy, R.; Andriatahina, T.; Randriamanantena, A.; Ravelomanana, L.; Randrianirina, F.; Richard, V. Etiologies, Risk Factors and Impact of Severe Diarrhea in the Under-Fives in Moramanga and Antananarivo, Madagascar PLoS One 2016, 11 (7) e0158862 DOI: 10.1371/journal.pone.0158862
  45. 45
    Headey, D.; Hirvonen, K. Is Exposure to Poultry Harmful to Child Nutrition? An Observational Analysis for Rural Ethiopia PLoS One 2016, 11 (8) e0160590 DOI: 10.1371/journal.pone.0160590
  46. 46
    Hetherington, J. B.; Wiethoelter, A. K.; Negin, J.; Mor, S. M. Livestock ownership, animal source foods and child nutritional outcomes in seven rural village clusters in Sub-Saharan Africa Agriculture and Food Security 2017, 6 (1) 9 DOI: 10.1186/s40066-016-0079-z
  47. 47
    Mosites, E.; Thumbi, S. M.; Otiang, E.; McElwain, T. F.; Njenga, M. K.; Rabinowitz, P. M.; Rowhani-Rahbar, A.; Neuhouser, M. L.; May, S.; Palmer, G. H.; Walson, J. L. Relations between Household Livestock Ownership, Livestock Disease, and Young Child Growth J. Nutr. 2016, 146 (5) 1118 1124 DOI: 10.3945/jn.115.225961
  48. 48
    George, C. M.; Oldja, L.; Biswas, S. K.; Perin, J.; Lee, G. O.; Ahmed, S.; Haque, R.; Sack, R. B.; Parvin, T.; Azmi, I. J.; Bhuyian, S. I.; Talukder, K. A.; Faruque, A. G. Fecal Markers of Environmental Enteropathy are Associated with Animal Exposure and Caregiver Hygiene in Bangladesh Am. J. Trop. Med. Hyg. 2015, 93 (2) 269 275 DOI: 10.4269/ajtmh.14-0694
  49. 49
    Campbell, D.; Elia, M.; Lunn, P. Growth faltering in rural Gambian infants is associated with impaired small intestinal barrier function, leading to endotoxemia and systematic inflammation J. Nutr. 2003, 133 (5) 1332 1338
  50. 50
    Goto, R.; Mascie-Taylor, C. G. N.; Lunn, P. G. Impact of intestinal permeability, inflammation status and parasitic infections on infant growth faltering in rural Bangladesh Br. J. Nutr. 2009, 101 (10) 1509 1516 DOI: 10.1017/S0007114508083554
  51. 51
    Guerrant, R. L.; Oriá, R. B.; Moore, S. R.; Oriá, M. O. B.; Lima, A. A. M. Malnutrition as an enteric infectious disease with long-term effects on child development Nutr. Rev. 2008, 66 (9) 487 505 DOI: 10.1111/j.1753-4887.2008.00082.x
  52. 52
    Humphrey, J. H. Child undernutrition, tropical enteropathy, toilets, and handwashing Lancet 2009, 374 (9694) 1032 1035 DOI: 10.1016/S0140-6736(09)60950-8
  53. 53
    Lunn, P. G.; Northrop-Clewes, C. A.; Downes, R. M. Intestinal permeability, mucosal injury, and growth faltering in Gambian infants Lancet 1991, 338 (8772) 907 910 DOI: 10.1016/0140-6736(91)91772-M
  54. 54
    Lunn, P. G. Growth retardation and stunting of children in developing countries Br. J. Nutr. 2002, 88 (2) 109 110 DOI: 10.1079/BJN2002652
  55. 55
    Ordiz, M. I.; Shaikh, N.; Trehan, I.; Maleta, K.; Stauber, J.; Shulman, R.; Devaraj, S.; Tarr, P. I.; Manary, M. J. Environmental Enteric Dysfunction is Associated with Poor Linear Growth and Can be Identified by Host Fecal mRNAs J. Pediatr. Gastroenterol. Nutr. 2016, 63 (5) 453 DOI: 10.1097/MPG.0000000000001315
  56. 56
    El-Tras, W. F.; Holt, H. R.; Tayel, A. A.; El-Kady, N. N. Campylobacter infections in children exposed to infected backyard poultry in Egypt Epidemiol. Infect. 2015, 143 (2) 308 315 DOI: 10.1017/S095026881400096X
  57. 57
    Marquis, G. S.; Ventura, G.; Gilman, R. H.; Porras, E.; Miranda, E.; Carbajal, L.; Pentafiel, M. Am. J. Public Health 1990, 80 (2) 146 149 DOI: 10.2105/AJPH.80.2.146
  58. 58
    Vasco, K.; Graham, J. P.; Trueba, G. Detection of Zoonotic Enteropathogens in Children and Domestic Animals in a Semirural Community in Ecuador Appl. Environ. Microbiol. 2016, 82 (14) 4218 4224 DOI: 10.1128/AEM.00795-16
  59. 59
    Moore, C. E.; Elwin, K.; Phot, N.; Seng, C.; Mao, S.; Suy, K.; Kumar, V.; Nader, J.; Bousfield, R.; Perera, S.; Bailey, J. W.; Beeching, N. J.; Day, N. P. J.; Parry, C. M.; Chalmers, R. M. Molecular Characterization of Cryptosporidium Species and Giardia duodenalis from Symptomatic Cambodian Children PLoS Neglected Trop. Dis. 2016, 10 (7) e0004822 DOI: 10.1371/journal.pntd.0004822
  60. 60
    Wanyiri, J. W.; Kanyi, H.; Maina, S.; Wang, D. E.; Steen, A.; Ngugi, P.; Kamau, T.; Waithera, T.; O’Connor, R.; Gachuhi, K.; Wamae, C. N.; Mwamburi, M.; Ward, H. D. Cryptosporidiosis in HIV/AIDS Patients in Kenya: Clinical Features, Epidemiology, Molecular Characterization and Antibody Responses Am. J. Trop. Med. Hyg. 2014, 91 (2) 319 328 DOI: 10.4269/ajtmh.13-0254
  61. 61
    Wumba, R.; Longo-Mbenza, B.; Menotti, J.; Mandina, M.; Kintoki, F.; Situakibanza, N. H.; Kakicha, M. K.; Zanga, J.; Mbanzulu-Makola, K.; Nseka, T.; Mukendi, J. P.; Kendjo, E.; Sala, J.; Thellier, M. Epidemiology, clinical, immune, and molecular profiles of microsporidiosis and cryptosporidiosis among HIV/AIDS patients Int. J. Gen. Med. 2012, 5, 603 611
  62. 62
    Anuar, T. S.; Azreen, S. N.; Salleh, F. M.; Moktar, N. Molecular epidemiology of giardiasis among Orang Asli in Malaysia: application of the triosephosphate isomerase gene BMC Infect. Dis. 2014, 14 (1) 78 DOI: 10.1186/1471-2334-14-78
  63. 63
    Alyousefi, N. A.; Mahdy, M. A.; Mahmud, R.; Lim, Y. A. Factors associated with high prevalence of intestinal protozoan infections among patients in Sana’a City, Yemen PLoS One 2011, 6 (7) e22044 DOI: 10.1371/journal.pone.0022044
  64. 64
    Li, X.-X.; Chen, J.-X.; Wang, L.-X.; Tian, L.-G.; Zhang, Y.-P.; Dong, S.-P.; Hu, X.-G.; Liu, J.; Wang, F.-F.; Wang, Y.; Yin, X.-M.; He, L.-J.; Yan, Q.-Y.; Zhang, H.-W.; Xu, B.-L.; Zhou, X.-N. Prevalence and risk factors of intestinal protozoan and helminth infections among pulmonary tuberculosis patients without HIV infection in a rural county in P. R. China Acta Trop. 2015, 149, 19 26 DOI: 10.1016/j.actatropica.2015.05.001
  65. 65
    Bern, C.; Kawai, V.; Vargas, D.; Rabke-Verani, J.; Williamson, J.; Chavez-Valdez, R.; Xiao, L.; Sulaiman, I.; Vivar, A.; Ticona, E.; Ñavincopa, M.; Cama, V.; Moura, H.; Secor, W.; Visvesvara, G.; Gilman, R. H. The Epidemiology of Intestinal Microsporidiosis in Patients with HIV/AIDS in Lima, Peru J. Infect. Dis. 2005, 191 (10) 1658 1664 DOI: 10.1086/429674
  66. 66
    Dwivedi, K. K.; Prasad, G.; Saini, S.; Mahajan, S.; Lal, S.; Baveja, U. K. Enteric Opportunistic Parasites among HIV Infected Individuals: Associated Risk Factors and Immune Status Jpn. J. Infect. Dis. 2007, 60, 76 81
  67. 67
    Bublitz, D. C.; Wright, P. C.; Bodager, J. R.; Rasambainarivo, F. T.; Bliska, J. B.; Gillespie, T. R. Epidemiology of Pathogenic Enterobacteria in Humans, Livestock, and Peridomestic Rodents in Rural Madagascar PLoS One 2014, 9 (7) e101456 DOI: 10.1371/journal.pone.0101456
  68. 68
    Leung, D.; Das, S.; Malek, M.; Ahmed, D.; Khanam, F.; Qadri, F.; Faruque, A.; Ryan, E. Non-typhoidal Salmonella gastroenteritis at a diarrheal hospital in Dhaka, Bangladesh, 1996–2011 Am. J. Trop. Med. Hyg. 2013, 88 (4) 661 669 DOI: 10.4269/ajtmh.12-0672
  69. 69
    Labrique, A. B.; Zaman, K.; Hossain, Z.; Saha, P.; Yunus, M.; Hossain, A.; Ticehurst, J.; Kmush, B.; Nelson, K. E. An Exploratory Case Control Study of Risk Factors for Hepatitis E in Rural Bangladesh PLoS One 2013, 8 (5) e61351 DOI: 10.1371/journal.pone.0061351
  70. 70
    Mpyet, C.; Lass, B. D.; Yahaya, H. B.; Solomon, A. W. Prevalence of and Risk Factors for Trachoma in Kano State, Nigeria PLoS One 2012, 7 (7) e40421 DOI: 10.1371/journal.pone.0040421
  71. 71
    Nigusie, A.; Berhe, R.; Gedefaw, M. Prevalence and associated factors of active trachoma among childeren aged 1–9 years in rural communities of Gonji Kolella district, West Gojjam zone, North West Ethiopia BMC Res. Notes 2015, 8 (1) 641 DOI: 10.1186/s13104-015-1529-6
  72. 72
    Cumberland, P.; Hailu, G.; Todd, J. Active trachoma in children aged three to nine years in rural communities in Ethiopia: prevalence, indicators and risk factors Trans. R. Soc. Trop. Med. Hyg. 2005, 99 (2) 120 127 DOI: 10.1016/j.trstmh.2004.03.011
  73. 73
    Reichert, F.; Pilger, D.; Schuster, A.; Lesshafft, H.; Guedes de Oliveira, S.; Ignatius, R.; Feldmeier, H. Prevalence and Risk Factors of Hookworm-Related Cutaneous Larva Migrans (HrCLM) in a Resource-Poor Community in Manaus, Brazil PLoS Neglected Trop. Dis. 2016, 10 (3) e0004514 DOI: 10.1371/journal.pntd.0004514
  74. 74
    Acosta-Jamett, G.; Weitzel, T.; Boufana, B.; Adones, C.; Bahamonde, A.; Abarca, K.; Craig, P. S.; Reiter-Owona, I. Prevalence and risk factors for echinococcal infection in a rural area of northern Chile: A household-based cross-sectional study PLoS Neglected Trop. Dis. 2014, 8 (8) 1 9 DOI: 10.1371/journal.pntd.0003090
  75. 75
    Chiodo, P.; Basualdo, J.; Ciarmela, L.; Pezzani, B.; Apezteguía, M.; Minvielle, M. Related factors to human toxocariasis in a rural community of Argentina Memorias do Instituto Oswaldo Cruz. 2006, 101 (4) 397 400 DOI: 10.1590/S0074-02762006000400009
  76. 76
    Fernando, S.; Wickramasinghe, V.; Kapilananda, G.; Devasurendra, R.; Amarasooriya, J.; Dayaratne, H. Epidemiological aspects and risk factors of Toxocariasis in pediatric population in Sri Lanka Southeast Asian J. Trop. Med. Public Health 2007, 38 (6) 983 990
  77. 77
    Subrata, I. M.; Suryadhi, N. T.; Mantik-Astawa, N.; Damriyasa, I. M. Epidemiological and molecular analysis of Taxoplasa gondii in faecal samples of house cats obtained from house of maternal in Bali Bali Medical Journal 2015, 4 (2) 68 75 DOI: 10.15562/bmj.v4i2.122
  78. 78
    Daniels, M. E.; Shrivastava, A.; Smith, W. A.; Sahu, P.; Odagiri, M.; Misra, P. R.; Panigrahi, P.; Suar, M.; Clasen, T.; Jenkins, M. W. Cryptosporidium and giardia in humans, domestic animals, and village water sources in rural India Am. J. Trop. Med. Hyg. 2015, 93 (3) 596 600 DOI: 10.4269/ajtmh.15-0111
  79. 79
    Schriewer, A.; Odagiri, M.; Wuertz, S.; Misra, P. R.; Panigrahi, P.; Clasen, T.; Jenkins, M. W. Human and animal fecal contamination of community water sources, stored drinking water and hands in rural India measured with validated microbial source tracking assays Am. J. Trop. Med. Hyg. 2015, 93 (3) 509 516 DOI: 10.4269/ajtmh.14-0824
  80. 80
    Daniels, M. E.; Smith, W. A.; Schmidt, W. P.; Clasen, T.; Jenkins, M. W. Modeling Cryptosporidium and Giardia in Ground and Surface Water Sources in Rural India: Associations with Latrines, Livestock, Damaged Wells, and Rainfall Patterns Environ. Sci. Technol. 2016, 50 (14) 7498 7507 DOI: 10.1021/acs.est.5b05797
  81. 81
    Lupindu, A. M.; Olsen, J. E.; Ngowi, H. A.; Msoffe, P. L. M.; Mtambo, M. M.; Scheutz, F.; Dalsgaard, A. Occurrence and characterization of Shiga toxin-producing Escherichia coli O157:H7 and other non-sorbitol-fermenting E. coli in cattle and humans in urban areas of Morogoro, Tanzania Vector-Borne and Zoonotic Diseases. 2014, 14 (7) 503 510 DOI: 10.1089/vbz.2013.1502
  82. 82
    Nyariki, D. M.; Mwang’ombe, A. W.; Thompson, D. M. Land-use change and livestock production challenges in an integrated system: the Masai-Mara ecosystem, Kenya J. Hum. Ecol. 2009, 26 (3) 11
  83. 83
    Wolking, D. J.; Clifford, D. L.; Kelly, T. R.; Kamani, E.; Smith, W. A.; Kazwala, R. R.; Mazet, J. A. K. Boma to banda - a disease sentinel concept for reduction of diarrhoea Pastoralism: Research, Policy and Practice 2016, 6 (1) 13 DOI: 10.1186/s13570-016-0059-8
  84. 84
    Sprenger, L. K.; Green, K. T.; Molento, M. B. Geohelminth contamination of public areas and epidemiological risk factors in Curitiba, Brazil Rev. Bras. Parasitol. Vet. 2014, 23 (1) 69 73 DOI: 10.1590/S1984-29612014009
  85. 85
    Tun, S.; Ithoi, I.; Mahmud, R.; Samsudin, N. I.; Heng, C. K.; Ling, L. Y. Detection of Helminth Eggs and Identification of Hookworm Species in Stray Cats, Dogs and Soil from Klang Valley, Malaysia PLoS One 2015, 10 (12) e0142231 DOI: 10.1371/journal.pone.0142231
  86. 86
    Boehm, A. B.; Wang, D.; Ercumen, A.; Shea, M.; Harris, A. R.; Shanks, O. C.; Kelty, C.; Ahmed, A.; Mahmud, Z. H.; Arnold, B. F.; Chase, C.; Kullmann, C.; Colford, J. M.; Luby, S. P.; Pickering, A. J. Occurrence of Host-Associated Fecal Markers on Child Hands, Household Soil, and Drinking Water in Rural Bangladeshi Households Environ. Sci. Technol. Lett. 2016, 3 (11) 393 398 DOI: 10.1021/acs.estlett.6b00382
  87. 87
    Harris, A. R.; Pickering, A. J.; Harris, M.; Doza, S.; Islam, M. S.; Unicomb, L.; Luby, S.; Davis, J.; Boehm, A. B. Ruminants Contribute Fecal Contamination to the Urban Household Environment in Dhaka, Bangladesh Environ. Sci. Technol. 2016, 50 (9) 4642 DOI: 10.1021/acs.est.5b06282
  88. 88
    Ngure, F. M.; Humphrey, J. H.; Mbuya, M. N. N.; Majo, F.; Mutasa, K.; Govha, M.; Mazarura, E.; Chasekwa, B.; Prendergast, A. J.; Curtis, V.; Boor, K. J.; Stoltzfus, R. J. Formative Research on Hygiene Behaviors and Geophagy among Infants and Young Children and Implications of Exposure to Fecal Bacteria Am. J. Trop. Med. Hyg. 2013, 89 (4) 709 716 DOI: 10.4269/ajtmh.12-0568
  89. 89
    Sultana, R.; Nahar, N.; Rimi, N. A.; Azad, S.; Islam, M. S.; Gurley, E. S.; Luby, S. P. Backyard poultry raising in Bangladesh: a valued resource for the villagers and a setting for zoonotic transmission of avian influenza. A qualitative study Rural and Remote Health 2012, 12 (1927) 1 14
  90. 90
    Uga, S.; Hoa, N. T.; Noda, S.; Moji, K.; Cong, L.; Aoki, Y.; Rai, S. K.; Fujimaki, Y. Parasite egg contamination of vegetables from a suburban market in Hanoi, Vietnam Nepal Med. College J. 2009, 11 (2) 75 78
  91. 91
    Scallan, E.; Hoekstra, R. M.; Angulo, F. J.; Tauxe, R. V.; Widdowson, M.-A.; Roy, S. L.; Jones, J. L.; Griffin, P. M. Foodborne Illness Acquired in the United States—Major Pathogens Emerging Infect. Dis. 2011, 17 (1) 7 15 DOI: 10.3201/eid1701.P11101
  92. 92
    a Mpalang, R. K.; Boreux, R.; Melin, P.; Akir Ni Bitiang, K.; Daube, G.; De Mol, P. Prevalence of Campylobacter among goats and retail goat meat in Congo J. Infect. Dev. Countries 2014, 8 (2) 168 175 DOI: 10.3855/jidc.3199
  93. 93
    Osbjer, K.; Boqvist, S.; Sokerya, S.; Kannarath, C.; San, S.; Davun, H.; Magnusson, U. Household practices related to disease transmission between animals and humans in rural Cambodia BMC Public Health 2015, 15 (1) 476 DOI: 10.1186/s12889-015-1811-5
  94. 94
    Anuar, T. S.; Sarhan Al-Mekhlafi, H. M.; Abdul Ghani, M. K.; Moktar, N. Prevalence and risk factors associated with Entamoeba histolytica/Entamoeba dispar/Entamoeba moshkovskii complex infection among different tribes of Malaysian aborigines Int. J. Infect. Dis. 2012, 16, e175 e176 DOI: 10.1016/j.ijid.2012.05.725
  95. 95
    Suwannarong, K.; Chapman, R. S. Characteristics associated with contact with rodents in, around, and outside homes in Khon Kaen Province, Thailand Am. J. Trop. Med. Hyg. 2015, 92 (4) 784 790 DOI: 10.4269/ajtmh.14-0195
  96. 96
    Vujcic, J.; Ram, P. K.; Hussain, F.; Unicomb, L.; Gope, P. S.; Abedin, J.; Mahmud, Z. H.; Sirajul Islam, M.; Luby, S. P. Toys and toilets: cross-sectional study using children’s toys to evaluate environmental faecal contamination in rural Bangladeshi households with different sanitation facilities and practices Trop. Med. Int. Health 2014, 19 (5) 528 536 DOI: 10.1111/tmi.12292
  97. 97
    Torondel, B.; Gyekye-Aboagye, Y.; Routray, P.; Boisson, S.; Schimdt, W.; Clasen, T. Laboratory development and field testing of sentinel toys to assess environmental faecal exposure of young children in rural India Trans. R. Soc. Trop. Med. Hyg. 2015, 109 (6) 386 392 DOI: 10.1093/trstmh/trv023
  98. 98
    Harvey, S. A.; Winch, P. J.; Leontsini, E.; Torres Gayoso, C.; López Romero, S.; Gilman, R. H.; Oberhelman, R. A. Domestic poultry-raising practices in a Peruvian shantytown: implications for control of Campylobacter jejuni-associated diarrhea Acta Trop. 2003, 86 (1) 41 54 DOI: 10.1016/S0001-706X(03)00006-8
  99. 99
    Arnold, B. F.; Null, C.; Luby, S. P.; Unicomb, L.; Stewart, C. P.; Dewey, K. G.; Ahmed, T.; Ashraf, S.; Christensen, G.; Clasen, T.; Dentz, H. N.; Fernald, L. C. H.; Haque, R.; Hubbard, A. E.; Kariger, P.; Leontsini, E.; Lin, A.; Njenga, S. M.; Pickering, A. J.; Ram, P. K.; Tofail, F.; Winch, P. J.; Colford, J. M. Cluster-randomised controlled trials of individual and combined water, sanitation, hygiene and nutritional interventions in rural Bangladesh and Kenya: the WASH Benefits study design and rationale BMJ. Open 2013, 3 (8) e003476 DOI: 10.1136/bmjopen-2013-003476
  100. 100
    Hussain, F. Continued household faecal contamination following a sanitation intervention in rural Bangladesh. Health Sci. Bull. 2013, 11 (1), 9–14 (En), 9–14 (Bengali).
  101. 101

    Sanitation Hygiene Infant Nutrition Efficacy

    Trial, T.; Humphrey, J. H.; Jones, A. D.; Manges, A.; Mangwadu, G.; Maluccio, J. A.; Mbuya, M. N.; Moulton, L. H.; Ntozini, R.; Prendergast, A. J.; Stoltzfus, R. J.; Tielsch, J. M. The Sanitation Hygiene Infant Nutrition Efficacy (SHINE) Trial: Rationale, Design, and Methods Clin. Infect. Dis. 2015, 61 (Suppl 7) S685 702
  102. 102
    Hall, D.; Alam, M. G. S.; Raha, S. K. Reducing risk of emerging infectious diseases in Bangladesh through ecohealth Int. J. Infect. Dis. 2012, 16, e38 DOI: 10.1016/j.ijid.2012.05.096
  103. 103
    Cassenote, A. J. F.; de Abreu Lima, A. R.; Pinto Neto, J. M.; Rubinsky-Elefant, G. Seroprevalence and Modifiable Risk Factors for Toxocara spp. in Brazilian Schoolchildren PLoS Neglected Trop. Dis. 2014, 8 (5) e2830 DOI: 10.1371/journal.pntd.0002830
  104. 104
    Smolders, A.; Rolls, R. J.; Ryder, D.; Watkinson, A.; Mackenzie, M. Cattle-derived microbial input to source water catchments: An experimental assessment of stream crossing modification J. Environ. Manage. 2015, 156, 143 149 DOI: 10.1016/j.jenvman.2015.03.052
  105. 105
    Harwood, V. J.; Staley, C.; Badgley, B. D.; Borges, K.; Korajkic, A. Microbial source tracking markers for detection of fecal contamination in environmental waters: relationships between pathogens and human health outcomes FEMS Microbiology Reviews. 2014, 38 (1) 1 40 DOI: 10.1111/1574-6976.12031
  106. 106
    Liu, J.; Gratz, J.; Amour, C.; Kibiki, G.; Becker, S.; Janaki, L.; Verweij, J. J.; Taniuchi, M.; Sobuz, S. U.; Haque, R.; Haverstick, D. M.; Houpt, E. R. A Laboratory-Developed TaqMan Array Card for Simultaneous Detection of 19 Enteropathogens Journal of Clinical Microbiology 2013, 51 (2) 472 480 DOI: 10.1128/JCM.02658-12
  107. 107
    Platts-Mills, J. A.; Babji, S.; Bodhidatta, L.; Gratz, J.; Haque, R.; Havt, A.; McCormick, B. J. J.; McGrath, M.; Olortegui, M. P.; Samie, A.; Shakoor, S.; Mondal, D.; Lima, I. F. N.; Hariraju, D.; Rayamajhi, B. B.; Qureshi, S.; Kabir, F.; Yori, P. P.; Mufamadi, B.; Amour, C.; Carreon, J. D.; Richard, S. A.; Lang, D.; Bessong, P.; Mduma, E.; Ahmed, T.; Lima, A. A. A. M.; Mason, C. J.; Zaidi, A. K. M.; Bhutta, Z. A.; Kosek, M.; Guerrant, R. L.; Gottlieb, M.; Miller, M.; Kang, G.; Houpt, E. R. Pathogen-specific burdens of community diarrhoea in developing countries: a multisite birth cohort study (MAL-ED) Lancet Global Health 2015, 3 (9) e564 e575 DOI: 10.1016/S2214-109X(15)00151-5
  108. 108
    McLellan, S. L.; Eren, A. M. Discovering new indicators of fecal pollution Trends Microbiol. 2014, 22 (12) 697 706 DOI: 10.1016/j.tim.2014.08.002
  109. 109
    McLeroy, K. R.; Bibeau, D.; Steckler, A.; Glanz, K. An Ecological Perspective on Health Promotion Programs Health Education Quarterly. 1988, 15 (4) 351 377 DOI: 10.1177/109019818801500401
  110. 110
    Mupawaenda, A. C.; Chawatama, S.; Muvavarirwa, P. Gender issues in livestock production: a case study of Zimbabwe Trop. Anim. Health Prod. 2009, 41 (7) 1017 DOI: 10.1007/s11250-008-9268-5
  111. 111
    WHO; UNICEF. WASH Post-2015: Proposed indicatorsfor drinkingwater, sanitation, and hygiene. WHO/UNICEF Joint Monitoring Programmefor Water Supply and Sanitation, Geneca. (2015.

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  14. Drew Capone, Aaron Bivins, Jackie Knee, Oliver Cumming, Rassul Nalá, Joe Brown. Quantitative Microbial Risk Assessment of Pediatric Infections Attributable to Ingestion of Fecally Contaminated Domestic Soils in Low-Income Urban Maputo, Mozambique. Environmental Science & Technology 2021, 55 (3) , 1941-1952. https://doi.org/10.1021/acs.est.0c06972
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  16. Erica R. Fuhrmeister, Ayse Ercumen, Amy J. Pickering, Kaitlyn M. Jeanis, Yoshika Crider, Mahaa Ahmed, Sara Brown, Mahfuja Alam, Debashis Sen, Sharmin Islam, Mir Himayet Kabir, Mahfuza Islam, Mahbubur Rahman, Laura H. Kwong, Benjamin F. Arnold, Stephen P. Luby, John M. Colford, Jr., Kara L. Nelson. Effect of Sanitation Improvements on Pathogens and Microbial Source Tracking Markers in the Rural Bangladeshi Household Environment. Environmental Science & Technology 2020, 54 (7) , 4316-4326. https://doi.org/10.1021/acs.est.9b04835
  17. Erica R. Fuhrmeister, Ayse Ercumen, Amy J. Pickering, Kaitlyn M. Jeanis, Mahaa Ahmed, Sara Brown, Benjamin F. Arnold, Alan E. Hubbard, Mahfuja Alam, Debashis Sen, Sharmin Islam, Mir Himayet Kabir, Laura H. Kwong, Mahfuza Islam, Leanne Unicomb, Mahbubur Rahman, Alexandria B. Boehm, Stephen P. Luby, John M. Colford, Jr., Kara L. Nelson. Predictors of Enteric Pathogens in the Domestic Environment from Human and Animal Sources in Rural Bangladesh. Environmental Science & Technology 2019, 53 (17) , 10023-10033. https://doi.org/10.1021/acs.est.8b07192
  18. Kelly K. Baker, Reid Senesac, Daniel Sewell, Ananya Sen Gupta, Oliver Cumming, Jane Mumma. Fecal Fingerprints of Enteric Pathogen Contamination in Public Environments of Kisumu, Kenya, Associated with Human Sanitation Conditions and Domestic Animals. Environmental Science & Technology 2018, 52 (18) , 10263-10274. https://doi.org/10.1021/acs.est.8b01528
  19. Deneke Wolde, Girmay Medhin, Haile Alemayehu, Genet Asfaw Tilahun, Kehabtimer Shiferaw Kotiso, Woinshet Hailu, Adane Mihret, Feyissa Regassa Senbato, Aklilu Feleke Haile, Tadesse Eguale. Determinants of diarrheal diseases among patients attending public health centers in Addis Ababa and Hossana, Ethiopia: a matched case–control study. Tropical Medicine and Health 2025, 53 (1) https://doi.org/10.1186/s41182-024-00675-4
  20. Abdul-Ganiyu Adams, Helene Akpene Garti, Humphrey Kwesi Garti. Drivers of inappropriate complementary feeding among children 6–23 months in Nalerigu municipality, North East Region, Ghana. Nutrire 2025, 50 (1) https://doi.org/10.1186/s41110-025-00326-6
  21. Zachary Butzin-Dozier, Yunwen Ji, Jeremy Coyle, Ivana Malenica, Elizabeth T. Rogawski McQuade, Jessica Anne Grembi, James A. Platts-Mills, Eric R. Houpt, Jay P. Graham, Shahjahan Ali, Md Ziaur Rahman, Mohammad Alauddin, Syeda L. Famida, Salma Akther, Md. Saheen Hossen, Palash Mutsuddi, Abul K. Shoab, Mahbubur Rahman, Md. Ohedul Islam, Rana Miah, Mami Taniuchi, Jie Liu, Sarah T. Alauddin, Christine P. Stewart, Stephen P. Luby, John M. Colford Jr., Alan E. Hubbard, Andrew N. Mertens, Audrie Lin, . Treatment heterogeneity of water, sanitation, hygiene, and nutrition interventions on child growth by environmental enteric dysfunction and pathogen status for young children in Bangladesh. PLOS Neglected Tropical Diseases 2025, 19 (2) , e0012881. https://doi.org/10.1371/journal.pntd.0012881
  22. Loïc Deblais, Belisa Usmael Ahmedo, Amanda Ojeda, Bahar Mummed, Yuke Wang, Yitagele Terefe Mekonnen, Yenenesh Demisie Weldesenbet, Kedir A. Hassen, Mussie Brhane, Sarah McKune, Arie H. Havelaar, Song Liang, Gireesh Rajashekara. Assessing fecal contamination from human and environmental sources using Escherichia coli as an indicator in rural eastern Ethiopian households—a cross-sectional study from the EXCAM project. Frontiers in Public Health 2025, 12 https://doi.org/10.3389/fpubh.2024.1484808
  23. Katie Allen, Effie Papargyropoulou, Ruth Wade, Barbara Evans. Evaluating the performance of humanure as a potting mix for lettuce ( Lactuca sativa ) seedlings. Urban Agriculture & Regional Food Systems 2025, 10 (1) https://doi.org/10.1002/uar2.70010
  24. Omololu Ebenezer Fagunwa, Thobile Mthiyane, Ayokunle Fagunwa, Kassim Idowu Olayemi, Alaoma Alozie, Helen Onyeaka, Adenike Akinsemolu, Adegbola Ojo. Priority regions for eliminating open defecation in Africa: implications for antimicrobial resistance. Environment, Development and Sustainability 2025, 27 (1) , 2675-2699. https://doi.org/10.1007/s10668-023-03992-6
  25. D. O. Oduori, P. M. Kitala, T. M. Wachira, E. Mulinge, T. Irungu, E. Zeyhle, R. Ofwete, S. Gabriël, P. B. Gathura, . Assessment of Human Taeniasis and Other Intestinal Parasites in Narok County, Kenya. Veterinary Medicine International 2025, 2025 (1) https://doi.org/10.1155/vmi/9226601
  26. Noor Mahmood Sultan, Abeer Abbas Ali, Hayder Jaleel Mardan. Isolation and Identification of the Types of Bacteria that Cause Irritable Bowel Syndrome. Medical Journal of Babylon 2025, 22 (1) , 17-22. https://doi.org/10.4103/MJBL.MJBL_185_22
  27. Nicholas Cowan, Will Brownlie, Samuel Tomlinson, Edward Carnell, Julia Drewer, Ulrike Dragosits, Peter Levy, Bryan M. Spears. A global assessment of nitrogen and phosphorus generated in the waste streams of domesticated cats and dogs. Sustainable Environment 2024, 10 (1) https://doi.org/10.1080/27658511.2024.2415181
  28. Eric Gbenatey Nartey, Ruben Sakrabani, Sean Tyrrel, Olufunke Cofie. Storage duration and temperature affect pathogen load, heavy metals, and nutrient levels in faecal derived fertiliser. Environmental Technology 2024, 45 (27) , 5827-5837. https://doi.org/10.1080/09593330.2024.2309479
  29. Laingshun Huoy, Sireyvathanak Vuth, Sophanith Hoeng, Chilean Chheang, Phalla Yi, Chenda San, Panha Chhim, Sopacphear Thorn, Bunsopheana Ouch, Dengrachda Put, Lyna Aong, Kongkea Phan, Leila Nasirzadeh, Siteng Tieng, Erik Bongcam-Rudloff, Susanna Sternberg-Lewerin, Sofia Boqvist. Prevalence of Salmonella spp. in meat, seafood, and leafy green vegetables from local markets and vegetable farms in Phnom Penh, Cambodia. Food Microbiology 2024, 124 , 104614. https://doi.org/10.1016/j.fm.2024.104614
  30. Atalay Getachew, Mesafint Molla, Amha Admasie, Muluken Azage Yenesew. Association between domestic animal exposure and diarrhea prevalence in under- five children in low- and middle-income countries: a systematic review and meta-analysis. BMC Pediatrics 2024, 24 (1) https://doi.org/10.1186/s12887-024-05084-4
  31. Jitendra Gautam, Rajendra Prasad Parajuli, Kishor Pandey. Prevalence and associated factors of intestinal parasitic infections in the Badi indigenous communities of Western Nepal. Journal of Health, Population and Nutrition 2024, 43 (1) https://doi.org/10.1186/s41043-024-00694-1
  32. Andrew F. Brouwer, Mondal H. Zahid, Marisa C. Eisenberg, Benjamin F. Arnold, Sania Ashraf, Jade Benjamin-Chung, John M. Colford, Ayse Ercumen, Stephen P. Luby, Amy J. Pickering, Mahbubur Rahman, Alicia N.M. Kraay, Joseph N.S. Eisenberg, Matthew C. Freeman. Understanding the Effectiveness of Water, Sanitation, and Hygiene Interventions: A Counterfactual Simulation Approach to Generalizing the Outcomes of Intervention Trials. Environmental Health Perspectives 2024, 132 (12) https://doi.org/10.1289/EHP15200
  33. Felipe Zampieri Vieira Batista, Igor Domingos de Souza, Diego Azevedo Zoccal Garcia, Daniela Granja Arakaki, Cláudia Stela de Araújo Medeiros, Marta Aratuza Pereira Ancel, Elaine Silva de Pádua Melo, Valter Aragão do Nascimento. Faeces of Capybara (Hydrochoerus hydrochaeris) as a Bioindicator of Contamination in Urban Environments in Central-West Brazil. Urban Science 2024, 8 (4) , 151. https://doi.org/10.3390/urbansci8040151
  34. Jonny Crocker, Emily Ogutu, Jedidiah S. Snyder, Antoinette Kome, Ben Tidwell, Jan Willem Rosenboom, Jesse Shapiro, Jessy Samuyachi Mahongo, Kelly T. Alexander, Michael E. Gnilo, Om Prasad Gautam, Sara Hoffman, Sovattha Neou, Matthew C. Freeman. TIDieR-WASH: A Guideline for Reporting Implementation of Water, Sanitation, and Hygiene Interventions. Environmental Health Perspectives 2024, 132 (11) https://doi.org/10.1289/EHP14780
  35. Sheetal Negi, Sarika Sharma. Ready to Eat Food: A Reason for Enhancement in Multidrug Resistance in Humans. Advanced Pharmaceutical Bulletin 2024, 14 (3) , 504-512. https://doi.org/10.34172/apb.2024.023
  36. Stephanie A. Houser, Daniel K. Sewell, Danielle N. Medgyesi, John M. Brogan, Jean Philippe Creve-Coeur, Kelly K. Baker, . A multi-pathogen behavioral exposure model for young children playing in public spaces in developing communities. PLOS Neglected Tropical Diseases 2024, 18 (10) , e0012564. https://doi.org/10.1371/journal.pntd.0012564
  37. Arun Sharma, Himansh Goel, Saurabh Sharma, Hanumant Singh Rathore, Imlitoshi Jamir, Abhishek Kumar, Shivasharana Chandrabanda Thimmappa, Kavindra Kumar Kesari, Brijendra Kumar Kashyap. Cutting edge technology for wastewater treatment using smart nanomaterials: recent trends and futuristic advancements. Environmental Science and Pollution Research 2024, 31 (48) , 58263-58293. https://doi.org/10.1007/s11356-024-34977-1
  38. Shengao Yi, Xiaojiang Li, Ruoyu Wang, Ziyi Guo, Xinyu Dong, Yixuan Liu, Qian Xu. Interpretable spatial machine learning insights into urban sanitation challenges: A case study of human feces distribution in San Francisco. Sustainable Cities and Society 2024, 113 , 105695. https://doi.org/10.1016/j.scs.2024.105695
  39. Sara de Wit, Euphrasia Luseka, David Bradley, Joe Brown, Jayant Bhagwan, Barbara Evans, Matthew C Freeman, Guy Howard, Isha Ray, Ian Ross, Sheillah Simiyu, Oliver Cumming, Clare I R Chandler. Water, sanitation and hygiene (WASH): the evolution of a global health and development sector. BMJ Global Health 2024, 9 (10) , e015367. https://doi.org/10.1136/bmjgh-2024-015367
  40. April M. Ballard, Regine Haardörfer, Betty Corozo Angulo, Matthew C. Freeman, Joseph N. S. Eisenberg, Gwenyth O. Lee, Karen Levy, Bethany A. Caruso, . The development and validation of a survey to measure fecal-oral child exposure to zoonotic enteropathogens: The FECEZ Enteropathogens Index. PLOS Global Public Health 2024, 4 (9) , e0002690. https://doi.org/10.1371/journal.pgph.0002690
  41. Jingjing Ding, Xinyuan Cui, Xuan Wang, Feifei Zhai, Lei Wang, Lifeng Zhu. Multi-omics analysis of gut microbiota and metabolites reveals contrasting profiles in domestic pigs and wild boars across urban environments. Frontiers in Microbiology 2024, 15 https://doi.org/10.3389/fmicb.2024.1450306
  42. Xinyuan Feng, Xianghua Xu, Xuewen Yao, Yujing Zhao, Yali Tang, Zhen Zhao, Yaqian Wei, Tariq Mehmood, Xiao-San Luo. Sources, compositions, spatio-temporal distributions, and human health risks of bioaerosols: A review. Atmospheric Research 2024, 305 , 107453. https://doi.org/10.1016/j.atmosres.2024.107453
  43. Siyuan Yang, Xiangqun Zheng, Jiaqi Hou, Bing Geng, Liangguo Luo, Changxiong Zhu, Liyuan Liu, Jie Zhu. Rural revival: Navigating environmental engineering and technology. Environmental Research 2024, 254 , 119164. https://doi.org/10.1016/j.envres.2024.119164
  44. Blessing Mberu, Sheillah Simiyu, Fanta D Gutema, Daniel Sewell, Phylis J Busienei, Innocent K Tumwebaze, Kelly K Baker. Landscape analysis of the Kenyan policy on the treatment and prevention of diarrheal disease among under-5 children. BMJ Open 2024, 14 (8) , e081906. https://doi.org/10.1136/bmjopen-2023-081906
  45. Meshack Achore. Understanding the seasonal variations in access to improved water sources in Ghana: A call to action for policymakers. AQUA — Water Infrastructure, Ecosystems and Society 2024, 73 (8) , 1754-1765. https://doi.org/10.2166/aqua.2024.201
  46. Alasdair Cohen, Md Rasheduzzaman, Bethesda O'Connell, Teresa Brown, Mami Taniuchi, Leigh-Anne Krometis, Alan Hubbard, Phillip Scheuerman, Marc Edwards, Amanda Darling, Blaine Pennala, Sarah Price, Breanna Lytton, Erin Wettstone, Suporn Pholwat, Honorine Ward, Daniel R. Hallinger, Steven O. Simmons, Shannon M. Griffin, Jason Kobylanski, Andrey I. Egorov, Timothy J. Wade. Drinking water sources, quality, and associated health outcomes in Appalachian Virginia: A risk characterization study in two counties. International Journal of Hygiene and Environmental Health 2024, 260 , 114390. https://doi.org/10.1016/j.ijheh.2024.114390
  47. Krity Rai, Anil Kumar Misra, Rakesh Kumar Ranjan, Nishchal Wanjari, Rajeev Rajak, Shailesh Kumar Yadav, Richard Rai, Md. Abdullah Khan. Assessment of Heavy Metal and E. coli Contamination in Water Sources of the East and South Districts, Sikkim Himalaya, India. Water Conservation Science and Engineering 2024, 9 (1) https://doi.org/10.1007/s41101-024-00257-9
  48. Jim Wright, Mawuli Dzodzomenyo, Allan G. Hill, Lorna G. Okotto, Mair L.H. Thomas-Possee, Peter J. Shaw, Joseph Okotto-Okotto. Integrating urban household solid waste management with WASH: Implications from case studies of monitoring in sub-Saharan Africa. Environmental Development 2024, 50 , 100990. https://doi.org/10.1016/j.envdev.2024.100990
  49. M. Khairuzzaman, Md Mehedi Hasan, Mohammad Tuhin Ali, Abdullah Al Mamun, Sheuly Akter, Papia Nasrin, Md Khirul Islam, Akhlak Un Nahar, Dipto Kumer Sarker, Omer Abdalla Ahmed Hamdi, Shaikh Jamal Uddin, Veronique Seidel, Jamil A. Shilpi. Anthelmintic screening of Bangladeshi medicinal plants and related phytochemicals using in vitro and in silico methods: An ethnobotanical perspective. Journal of Ethnopharmacology 2024, 328 , 118132. https://doi.org/10.1016/j.jep.2024.118132
  50. Donald Fejfar, Wren Tracy, Emma Kelly, Michelle Moffa, Robert Bain, Jamie Bartram, Darcy Anderson, Ryan Cronk. Identifying predictors of E. coli in rural household water in sub-Saharan Africa using elimination regression. Environmental Science: Water Research & Technology 2024, 10 (5) , 1147-1159. https://doi.org/10.1039/D3EW00915G
  51. Aly El Riz, Armelle Tchoumi Neree, Leila Mousavifar, René Roy, Younes Chorfi, Mircea Alexandru Mateescu. Metallo-Glycodendrimeric Materials against Enterotoxigenic Escherichia coli. Microorganisms 2024, 12 (5) , 966. https://doi.org/10.3390/microorganisms12050966
  52. Olutayo Israel Falodun, Akeem Ganiyu Rabiu, Abidemi Joseph Marcus, Rotimi Ayodeji Dada, Mobolaji Christianah Afolabi. Characterization of virulent Escherichia coli in healthy pet dog feces: Implications for public health. Journal of Istanbul Veterinary Sciences 2024, 8 (1) , 5-12. https://doi.org/10.30704/http-www-jivs-net.1407165
  53. Michael J. Ormsby, Luke Woodford, Richard S. Quilliam. Can plastic pollution drive the emergence and dissemination of novel zoonotic diseases?. Environmental Research 2024, 246 , 118172. https://doi.org/10.1016/j.envres.2024.118172
  54. Joseph Wells, David Gama Abugo, John Angong, Nancy Grace Lamwaka, Karin Gallandat, Jackson Lwate Hassan, Lino Deng, Dimple Save, Laura Braun, Mesfin Gose, Jacob Amanya, Khamisa Ayoub, Sarah King, Heather Stobaugh, Oliver Cumming, Lauren D'Mello‐Guyett. Risk factors for food contamination among children discharged from community management of acute malnutrition programmes in South Sudan: A cross‐sectional study and hazard analysis critical control point approach. Maternal & Child Nutrition 2024, 20 (2) https://doi.org/10.1111/mcn.13612
  55. Callum Lowe, Haribondhu Sarma, Darren Gray, Matthew Kelly. Perspective: Connecting the dots between domestic livestock ownership and child linear growth in low‐ and middle‐income countries. Maternal & Child Nutrition 2024, 20 (2) https://doi.org/10.1111/mcn.13618
  56. Horthing V. Zimik, Anil Kumar Misra, Rakesh Kr. Ranjan, Nishchal Wanjari, Smriti Basnett, Goshaidas Roy, Anirudra Rai, Khushboo Sharma, Manish Kumar Keshare, Swapan Dolui. Evaluation of heavy metal and microbial contamination in various water resources of West and North Sikkim, India. Environment, Development and Sustainability 2024, 26 (3) , 7947-7972. https://doi.org/10.1007/s10668-023-03044-z
  57. Giulia Granai, Carmen Borrelli, Chiara Mariti, Francesco Di Iacovo. Animals and Cities: A Reflection on Their Potential in Innovating Nature-Based Solutions. Animals 2024, 14 (5) , 680. https://doi.org/10.3390/ani14050680
  58. John J. Hart, Megan N. Jamison, Alexis M. Porter, James N. McNair, David C. Szlag, Richard R. Rediske. Fecal Impairment Framework, A New Conceptual Framework for Assessing Fecal Contamination in Recreational Waters. Environmental Management 2024, 73 (2) , 443-456. https://doi.org/10.1007/s00267-023-01878-x
  59. Paula Dominguez-Salas, Hugh Sharma Waddington, Delia Grace, Caroline Bosire, Arshnee Moodley, Bharati Kulkarni, Teena Dasi, Santosh Kumar Banjara, Ramachandrappa Naveen Kumar, Umi Fahmida, Min Kyaw Htet, Arienta R P Sudibya, Babacar Faye, Roger C Tine, Claire Heffernan, Deepak Saxena, Robert Dreibelbis, B Häsler. Understanding the role of household hygiene practices and foodborne disease risks in child stunting: a UKRI GCRF Action Against Stunting Hub protocol paper. BMJ Paediatrics Open 2024, 8 (Suppl 1) , e001695. https://doi.org/10.1136/bmjpo-2022-001695
  60. Kiran Kumar Vadde, Sina V. Moghadam, Arash Jafarzadeh, Akanksha Matta, Duc C. Phan, Drew Johnson, Vikram Kapoor, . Precipitation impacts the physicochemical water quality and abundance of microbial source tracking markers in urban Texas watersheds. PLOS Water 2024, 3 (2) , e0000209. https://doi.org/10.1371/journal.pwat.0000209
  61. Nur Maizatul Idayu Othman, Aida Soraya Shamsuddin, Norazlina Abu Sari, Zaiton Sapak, Samihah Mustaffha, Sharifah Norkhadijah Syed Ismail, Abdul Rahman Saili. Types and factors of waste accumulation. 2024, 43-80. https://doi.org/10.1016/B978-0-443-13847-8.00002-6
  62. Yiyi Su, Fang Huang, Zihan Dai, Ai-Jie Wang, Shu-Hong Gao. Environmental ecology and health risk assessment of pathogens in the environment. 2024, 99-121. https://doi.org/10.1016/B978-0-443-14170-6.00028-7
  63. Rama Rao Karri, Nabisab Mujawar Mubarak, Suraj Kumar Bhagat, Tiyasha Tiyasha, Lakshmi Prasanna Lingamdinne, Janardhan Reddy Koduru, Gobinath Ravindran, Inderjeet Tyagi, Mohammad Hadi Dehghani. Scientometrics and overview of water, environment, and sustainable development goals. 2024, 3-33. https://doi.org/10.1016/B978-0-443-15354-9.00021-9
  64. V. Sharma, P. Kaur, R.S. Aulakh, R. Sharma, R. Verma, B.B. Singh. Is Brucella excreted in cattle faeces? – Evidence from Punjab, India. Comparative Immunology, Microbiology and Infectious Diseases 2024, 104 , 102099. https://doi.org/10.1016/j.cimid.2023.102099
  65. Fa Shan, Qingda Meng, Fang Wang, Jinfeng Zhao, Huiyan Xu, Nanhao Wang, Yufeng Liu, Sumei Zhang, Guanghui Zhao, Longxian Zhang. Wild sympatric rodents inhabiting pig farm environments may facilitate the spillover of Enterocytozoon bieneusi from pig farms. Parasite 2024, 31 , 59. https://doi.org/10.1051/parasite/2024061
  66. Zemichael Gizaw, Alemayehu Worku Yalew, Bikes Destaw Bitew, Jiyoung Lee, Michael Bisesi. Animal Handling Practice Among Rural Households in Northwest Ethiopia Increases the Risk of Childhood Diarrhea and Exposure to Pathogens From Animal Sources. Environmental Health Insights 2024, 18 https://doi.org/10.1177/11786302241245057
  67. Dikeledi Prudence Mothiba, Colette Mmapenya Khabo-Mmekoa, Renay Ngobeni-Nyambi, Maggy Ndombo Benteke Momba. Assessing the Occurrence of Host-Specific Faecal Indicator Markers in Water Systems as a Function of Water, Sanitation and Hygiene Practices: A Case Study in Rural Communities of Vhembe District Municipality, South Africa. Pathogens 2024, 13 (1) , 16. https://doi.org/10.3390/pathogens13010016
  68. Randi L. Rollins, Matthew C.I. Medeiros, Robert H. Cowie. Stressed snails release Angiostrongylus cantonensis (rat lungworm) larvae in their slime. One Health 2023, 17 , 100658. https://doi.org/10.1016/j.onehlt.2023.100658
  69. Manjari Manisha, Kavita Verma, N. Ramesh, T.P. Anirudha, R.M. Santrupt, Lakshminarayana Rao. Water, sanitation, and hygiene implications of large-scale recycling of treated municipal wastewater in semi-arid regions. Science of The Total Environment 2023, 904 , 166631. https://doi.org/10.1016/j.scitotenv.2023.166631
  70. Anni Juvakoski, Henrik Rantanen, Michela Mulas, Francesco Corona, Riku Vahala, Olli Varis, Ilkka Mellin. Evidence of waste management impacting severe diarrhea prevalence more than WASH: An exhaustive analysis with Brazilian municipal-level data. Water Research 2023, 247 , 120805. https://doi.org/10.1016/j.watres.2023.120805
  71. Taddese Alemu Zerfu, Giang Nguyen, Alan J. Duncan, Isabelle Baltenweck, Fiona Brown, Lora L. Iannotti, Geraldine McNeill. Associations between livestock keeping, morbidity and nutritional status of children and women in low- and middle-income countries: a systematic review. Nutrition Research Reviews 2023, 36 (2) , 526-543. https://doi.org/10.1017/S0954422422000233
  72. Derrick N. Sentamu, Joseph Kungu, Michel Dione, Lian F. Thomas. Prevention of human exposure to livestock faecal waste in the household: a scoping study of interventions conducted in sub-Saharan Africa. BMC Public Health 2023, 23 (1) https://doi.org/10.1186/s12889-023-16567-x
  73. Molly Mills, Seungjun Lee, Barbara A. Piperata, Rebecca Garabed, Boseung Choi, Jiyoung Lee. Household environment and animal fecal contamination are critical modifiers of the gut microbiome and resistome in young children from rural Nicaragua. Microbiome 2023, 11 (1) https://doi.org/10.1186/s40168-023-01636-5
  74. Hugo Legge, Rachel L. Pullan, Benn Sartorius, . Improved household flooring is associated with lower odds of enteric and parasitic infections in low- and middle-income countries: A systematic review and meta-analysis. PLOS Global Public Health 2023, 3 (12) , e0002631. https://doi.org/10.1371/journal.pgph.0002631
  75. Yudith Vega Paramitadevi, Cindy Rianti Priadi, Iftita Rahmatika, Andriansjah Rukmana, Setyo Sarwanto Moersidik. Integration of water, sanitation, and hygiene program with biosecurity: A One Health approach to reduce the prevalence and exposure of antibiotic-resistant bacteria in the livestock community. International Journal of One Health 2023, , 181-193. https://doi.org/10.14202/IJOH.2023.181-193
  76. Drew Capone, Toheedat Bakare, Troy Barker, Amy Hutson Chatham, Ryan Clark, Lauren Copperthwaite, Abeoseh Flemister, Riley Geason, Emery Hoos, Elizabeth Kim, Alka Manoj, Sam Pomper, Christina Samodal, Simrill Smith, Claudette Poole, Joe Brown. Risk Factors for Enteric Pathogen Exposure among Children in Black Belt Region of Alabama, USA. Emerging Infectious Diseases 2023, 29 (12) https://doi.org/10.3201/eid2912.230780
  77. Tanja Zlender, Maja Rupnik. An overview of molecular markers for identification of non-human fecal pollution sources. Frontiers in Microbiology 2023, 14 https://doi.org/10.3389/fmicb.2023.1256174
  78. Peter Kirira, Fiona Oyatsi, Ashley Waudo, Samuel Mbugua. Improving Access to Safe Water in Rural Schools of Kenya: Qualitative Multisectoral Insights. Cureus 2023, 85 https://doi.org/10.7759/cureus.49174
  79. M. Mehrab Bakhtiar, John Hoddinott. Household dairy production, dairy intake, and anthropometric outcomes in rural Bangladesh. Food Policy 2023, 121 , 102567. https://doi.org/10.1016/j.foodpol.2023.102567
  80. Valliappan Muthu, Ritesh Agarwal, Arunaloke Chakrabarti. Cow dung, COVID-19, and mucormycosis … more damned lies. Indian Journal of Medical Microbiology 2023, 46 , 100464. https://doi.org/10.1016/j.ijmmb.2023.100464
  81. Frederica Lamar, Hermógenes N. Mucache, Amelia Mondlane-Milisse, Kelsey J. Jesser, Courtney Victor, José M. Fafetine, Joaquim Ângelo Osvaldo Saíde, Eric M. Fèvre, Bethany A. Caruso, Matthew C. Freeman, Karen Levy. Quantifying Enteropathogen Contamination along Chicken Value Chains in Maputo, Mozambique: A Multidisciplinary and Mixed-Methods Approach to Identifying High Exposure Settings. Environmental Health Perspectives 2023, 131 (11) https://doi.org/10.1289/EHP11761
  82. Heather K. Amato, Fernanda Loayza, Liseth Salinas, Diana Paredes, Daniela Garcia, Soledad Sarzosa, Carlos Saraiva-Garcia, Timothy J. Johnson, Amy J. Pickering, Lee W. Riley, Gabriel Trueba, Jay P. Graham. Risk factors for extended-spectrum beta-lactamase (ESBL)-producing E. coli carriage among children in a food animal-producing region of Ecuador: A repeated measures observational study. PLOS Medicine 2023, 20 (10) , e1004299. https://doi.org/10.1371/journal.pmed.1004299
  83. Valerie L. Flax, Emily A. Ouma, Isabelle Baltenweck, Esther Omosa, Amy Webb Girard, Nathaniel Jensen, Paula Dominguez-Salas. Pathways from livestock to improved human nutrition: lessons learned in East Africa. Food Security 2023, 15 (5) , 1293-1312. https://doi.org/10.1007/s12571-023-01382-4
  84. Aulo Gelli, Anissa Collishaw, Josue Awonon, Elodie Becquey, Ampa Diatta, Loty Diop, Rasmane Ganaba, Derek Headey, Alain Hien, Francis Ngure, Abdoulaye Pedehombga, Marco Santacroce, Laeticia C. Toe, Hans Verhoef, Harold Alderman, Marie T. Ruel. Effects of an integrated poultry value chain, nutrition, gender and WASH intervention (SELEVER) on hygiene and child morbidity and anthropometry in Burkina Faso: A secondary outcome analysis of a cluster randomised trial. Maternal & Child Nutrition 2023, 19 (4) https://doi.org/10.1111/mcn.13528
  85. Anissa Collishaw, Sarah Janzen, Conner Mullally, Hannah Camilli. A review of livestock development interventions’ impacts on household welfare in low- and middle-income countries. Global Food Security 2023, 38 , 100704. https://doi.org/10.1016/j.gfs.2023.100704
  86. Onyenweife Geraldine Ifesinachi, Onyenweife Leonard Chikwado. Evaluation of Water Contamination and Its Health Implications on the Residents of Ayamelum Local Government Area, Anambra State, Nigeria. Asian Journal of Geographical Research 2023, 6 (3) , 1-8. https://doi.org/10.9734/ajgr/2023/v6i3184
  87. Troy Barker, Drew Capone, Heather K. Amato, Ryan Clark, Abigail Henderson, David A. Holcomb, Elizabeth Kim, Jillian Pape, Emily Parker, Thomas VanderYacht, Jay Graham, Joe Brown, . Public toilets have reduced enteric pathogen hazards in San Francisco. PLOS Water 2023, 2 (8) , e0000152. https://doi.org/10.1371/journal.pwat.0000152
  88. Leigh C. Hamlet, Suman Chakrabarti, Jessica Kaminsky. Environmental sanitation and undernutrition among China’s children and adolescents from 1989 to 2011. Nature Water 2023, 1 (8) , 736-749. https://doi.org/10.1038/s44221-023-00112-6
  89. Josphat Muema, Nyamai Mutono, Stevens Kisaka, Brian Ogoti, Julius Oyugi, Zipporah Bukania, Tewoldeberhan Daniel, Joseph Njuguna, Irene Kimani, Anita Makori, Sylvia Omulo, Erin Boyd, Abdal Monium Osman, Luc Gwenaelle, Christine Jost, SM Thumbi. The impact of livestock interventions on nutritional outcomes of children younger than 5 years old and women in Africa: a systematic review and meta-analysis. Frontiers in Nutrition 2023, 10 https://doi.org/10.3389/fnut.2023.1166495
  90. Muhiuddin Haider, Sameen Ahmed, Allysha Choudhary. One Health: Implementation Challenges and Need. 2023https://doi.org/10.5772/intechopen.111933
  91. Melodie Sammarro, Barry Rowlingson, Derek Cocker, Kondwani Chidziwisano, Shevin T Jacob, Henry Kajumbula, Lawrence Mugisha, David Musoke, Rebecca Lester, Tracy Morse, Nicholas Feasey, Chris Jewell. Risk Factors, Temporal Dependence, and Seasonality of Human Extended-Spectrum β-Lactamases-Producing Escherichia coli and Klebsiella pneumoniae Colonization in Malawi: A Longitudinal Model-Based Approach. Clinical Infectious Diseases 2023, 77 (1) , 1-8. https://doi.org/10.1093/cid/ciad117
  92. Kayla C. Lanker, Abdifatah M. Muhummed, Guéladio Cissé, Jakob Zinsstag, Jan Hattendorf, Ramadan Budul Yusuf, Shamil Barsenga Hassen, Rea Tschopp, Pascale Vonaesch, . Prevalence and associated risk factors of intestinal parasitic infections among children in pastoralist and agro-pastoralist communities in the Adadle woreda of the Somali Regional State of Ethiopia. PLOS Neglected Tropical Diseases 2023, 17 (7) , e0011448. https://doi.org/10.1371/journal.pntd.0011448
  93. Marcin Sońta, Justyna Więcek, Ewa Szara, Anna Rekiel, Anna Zalewska, Martyna Batorska. Quantitative and Qualitative Traits of Duckweed (Lemna minor) Produced on Growth Media with Pig Slurry. Agronomy 2023, 13 (7) , 1951. https://doi.org/10.3390/agronomy13071951
  94. Farshad Amiraslani. You Are Not Welcome! A Media Analysis of Risk Factors, Prevalence and Management of Free-Roaming Dogs in Iran. Animals 2023, 13 (14) , 2347. https://doi.org/10.3390/ani13142347
  95. Ali Jahanmahin, Hassan Borji. Unveiling the Zoonotic Significance of Toxocariasis in Humans: The Role of Toxocara canis. Small Animal Advances 2023, 2 (2) , 5-11. https://doi.org/10.58803/saa.v2i2.14
  96. Andrea Dias-Alves, Johan Espunyes, Teresa Ayats, Celsus Sente, Peregrine Sebulime, Jesus Muro, Josephine Tushabe, Caroline Asiimwe, Xavier Fernandez Aguilar, Robert Aruho, Ignasi Marco, Marta Planellas, Jesús Cardells, Oscar Cabezón, Marta Cerdà-Cuéllar. Foodborne Pathogens at the Livestock–Wildlife–Human Interface in Rural Western Uganda. EcoHealth 2023, 20 (2) , 144-149. https://doi.org/10.1007/s10393-023-01639-6
  97. Katharine Conaway, Sarah Lebu, Kylie Heilferty, Aaron Salzberg, Musa Manga. On-site sanitation system emptying practices and influential factors in Asian low- and middle-income countries: A systematic review. Hygiene and Environmental Health Advances 2023, 6 , 100050. https://doi.org/10.1016/j.heha.2023.100050
  98. Arthur Moses, Mónica D Ramírez-Andreotta, Jean E T McLain, Luz Imelda Cortez, Aminata Kilungo. Assessing the impact of rainwater harvesting infrastructure and gardening trends on microbial indicator organism presence in harvested rainwater and garden soils. Journal of Applied Microbiology 2023, 134 (6) https://doi.org/10.1093/jambio/lxad110
  99. Sayan Bhattacharyya, Sri Krishna Vinay Triparagiri, Subhrajeet Chakraborty, Amit Banik, Atul Raj. A study on prevalence of Intestinal worm infestation and a comparative analysis between two floatation methods, for demonstrating intestinal parasites in stool (dung) of cattle. IP International Journal of Medical Microbiology and Tropical Diseases 2023, 9 (1) , 31-35. https://doi.org/10.18231/j.ijmmtd.2023.006
  100. David M Berendes, Kirsten Fagerli, Sunkyung Kim, Dilruba Nasrin, Helen Powell, Irene N Kasumba, Sharon M Tennant, Anna Roose, M Jahangir Hossain, Joquina Chiquita M Jones, Syed M A Zaman, Richard Omore, John B Ochieng, Jennifer R Verani, Marc-Alain Widdowson, Samba O Sow, Sanogo Doh, Ciara E Sugerman, Eric D Mintz, Karen L Kotloff. Survey-Based Assessment of Water, Sanitation, and Animal-Associated Risk Factors for Moderate-to-Severe Diarrhea in the Vaccine Impact on Diarrhea in Africa (VIDA) Study: The Gambia, Mali, and Kenya, 2015–2018. Clinical Infectious Diseases 2023, 76 (Supplement_1) , S132-S139. https://doi.org/10.1093/cid/ciac911
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Cite this: Environ. Sci. Technol. 2017, 51, 20, 11537–11552
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Published September 19, 2017

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  • Abstract

    Figure 1

    Figure 1. Traditional F-Diagram showing potential fecal-oral transmission pathways. Adapted from Wagner, E.; Lanoix, J., Excreta disposal for rural areas and small communities. Monograph Series World Health Organization.1958, 39, 182. Copyright 1958, World Health Organization.

    Figure 2

    Figure 2. Impact of exposure to animal feces and/or contact with animals to human health.

    Figure 3

    Figure 3. Modified F-diagram showing transmission routes of animal feces to humans. Adapted from Wagner, E.; Lanoix, J., Excreta disposal for rural areas and small communities. Monograph Series World Health Organization.1958, 39, 182. Copyright 1958, World Health Organization.

    Figure 4

    Figure 4. Modified F-diagram including interventions that can block human exposure to animal feces. Adapted from Wagner, E.; Lanoix, J., Excreta disposal for rural areas and small communities. Monograph Series World Health Organization.1958, 39, 182. Copyright 1958, World Health Organization.

    Figure 5

    Figure 5. Priority research gaps in assessing human health impacts from exposure to poorly managed animal feces. This figure, an adaption from the socio-ecological model, represents how the “spheres of influence,” from human host and zoonotic pathogen biology to national policies, influence the health of the human host. Example items for future research within each sphere are provided.

  • References


    This article references 111 other publications.

    1. 1
      Jones, K. E.; Patel, N. G.; Levy, M. A.; Storeygard, A.; Balk, D.; Gittleman, J. L.; Daszak, P. Global trends in emerging infectious diseases Nature 2008, 451 (7181) 990 993 DOI: 10.1038/nature06536
    2. 2
      World Health Organization. The Control of Neglected Zoonotic Diseases: A Route to Poverty Alleviation: Report of a Joint WHO/DFID-AHP Meeting; WHO: Geneva, Switzerland, 2006.
    3. 3
      Wagner, E.; Lanoix, J. Excreta disposal for rural areas and small communities Monogr Ser. World Health Org. 1958, 39, 182
    4. 4
      Food and Agricultural Organization FAOSTAT. http://www.fao.org/faostat/en/#home (accessed 7 February 2017) .
    5. 5
      Zambrano, L. D.; Levy, K.; Menezes, N. P.; Freeman, M. C. Human diarrhea infections associated with domestic animal husbandry: a systematic review and meta-analysis Trans. R. Soc. Trop. Med. Hyg. 2014, 108 (6) 313 325 DOI: 10.1093/trstmh/tru056
    6. 6
      Batz, M. B.; Henke, E.; Kowalcyk, B. Long-term consequences of foodborne infections Infectious disease clinics of North America. 2013, 27 (3) 599 616 DOI: 10.1016/j.idc.2013.05.003
    7. 7
      Moore, S. R.; Lima, N. L.; Soares, A. M.; Oriá, R. B.; Pinkerton, R. C.; Barrett, L. J.; Guerrant, R. L.; Lima, A. A. Prolonged episodes of acute diarrhea reduce growth and increase risk of persistent diarrhea in children Gastroenterology 2010, 139 (4) 1156 1164 DOI: 10.1053/j.gastro.2010.05.076
    8. 8
      Lorntz, B.; Soares, A. M.; Moore, S. R.; Pinkerton, R.; Gansneder, B.; Bovbjerg, V. E.; Guyatt, H.; Lima, A. M.; Guerrant, R. L. Early childhood diarrhea predicts impaired school performance Pediatric infectious disease journal 2006, 25 (6) 513 520 DOI: 10.1097/01.inf.0000219524.64448.90
    9. 9
      Robert-Gangneux, F.; Dardé, M.-L. Epidemiology of and diagnostic strategies for toxoplasmosis Clin. Microbiol. Rev. 2012, 25 (2) 264 296 DOI: 10.1128/CMR.05013-11
    10. 10
      Wang, H.; Naghavi, M.; Allen, C.; Barber, R. M.; Bhutta, Z. A.; Carter, A.; Casey, D. C.; Charlson, F. J.; Chen, A. Z.; Coates, M. M.; al, e. Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death: a systematic analysis for the Global Burden of Disease Study Lancet. 2015, 388 (10053) 1459 1544
    11. 11
      Kotloff, K. L.; Nataro, J. P.; Blackwelder, W. C.; Nasrin, D.; Farag, T. H.; Panchalingam, S.; Wu, Y.; Sow, S. O.; Sur, D.; Breiman, R. F.; Faruque, A. S. G.; Zaidi, A. K. M.; Saha, D.; Alonso, P. L.; Tamboura, B.; Sanogo, D.; Onwuchekwa, U.; Manna, B.; Ramamurthy, T.; Kanungo, S.; Ochieng, J. B.; Omore, R.; Oundo, J. O.; Hossain, A.; Das, S. K.; Ahmed, S.; Qureshi, S.; Quadri, F.; Adegbola, R. A.; Antonio, M.; Hossain, M. J.; Akinsola, A.; Mandomando, I.; Nhampossa, T.; Acácio, S.; Biswas, K.; O’Reilly, C. E.; Mintz, E. D.; Berkeley, L. Y.; Muhsen, K.; Sommerfelt, H.; Robins-Browne, R. M.; Levine, M. M. Burden and aetiology of diarrhoeal disease in infants and young children in developing countries (the Global Enteric Multicenter Study, GEMS): a prospective, case-control study Lancet 2013, 382 (9888) 209 222 DOI: 10.1016/S0140-6736(13)60844-2
    12. 12
      Dufour, A.; Bartram, J.; Bos, R.; Gannon, V. Animal Waste, Water Quality and Human Health; IWA Publishing: London, UK, 2012, 6 130.
    13. 13
      Clasen, T. F.; Bostoen, K.; Schmidt, W.-P.; Boisson, S.; Fung, I. C. H.; Jenkins, M. W.; Scott, B.; Sugden, S.; Cairncross, S., Interventions to improve disposal of human excreta for preventing diarrhoea. Cochrane Database of Systematic Reviews 2010, (6). doi:  DOI: 10.1002/14651858.CD007180.pub2 .
    14. 14
      Stocks, M. E.; Ogden, S.; Haddad, D.; Addiss, D. G.; McGuire, C.; Freeman, M. C. Effect of Water, Sanitation, and Hygiene on the Prevention of Trachoma: A Systematic Review and Meta-Analysis PLoS Medicine. 2014, 11 (2) e1001605 DOI: 10.1371/journal.pmed.1001605
    15. 15
      Strunz, E. C.; Addiss, D. G.; Stocks, M. E.; Ogden, S.; Utzinger, J.; Freeman, M. C. Water, Sanitation, Hygiene, and Soil-Transmitted Helminth Infection: A Systematic Review and Meta-Analysis PLoS Medicine. 2014, 11 (3) e1001620 DOI: 10.1371/journal.pmed.1001620
    16. 16
      Barreto, M. L.; Genser, B.; Strina, A.; Assis, A. M. O.; Rego, R. F.; Teles, C. A.; Prado, M. S.; Matos, S. M. A.; Santos, D. N.; dos Santos, L. A.; Cairncross, S.; Teixeira, M. G. Effect of city-wide sanitation programme on reduction in rate of childhood diarrhoea in northeast Brazil: assessment by two cohort studies Lancet 2007, 370 (9599) 1622 1628 DOI: 10.1016/S0140-6736(07)61638-9
    17. 17
      Clasen, T.; Boisson, S.; Routray, P.; Torondel, B.; Bell, M.; Cumming, O.; Ensink, J.; Freeman, M.; Jenkins, M.; Odagiri, M.; Ray, S.; Sinha, A.; Suar, M.; Schmidt, W.-P. Effectiveness of a rural sanitation programme on diarrhoea, soil-transmitted helminth infection, and child malnutrition in Odisha, India: a cluster-randomised trial Lancet Global Health 2014, 2 (11) e645 e653 DOI: 10.1016/S2214-109X(14)70307-9
    18. 18
      Emerson, P. M.; Lindsay, S. W.; Alexander, N.; Bah, M.; Dibba, S.-M.; Faal, H. B.; Lowe, K.; McAdam, K. P. W. J.; Ratcliffe, A. A.; Walraven, G. E. L.; Bailey, R. L. Role of flies and provision of latrines in trachoma control: cluster-randomised controlled trial Lancet 2004, 363 (9415) 1093 1098 DOI: 10.1016/S0140-6736(04)15891-1
    19. 19
      Patil, S. R.; Arnold, B. F.; Salvatore, A. L.; Briceno, B.; Ganguly, S.; Colford, J. M., Jr.; Gertler, P. J. The Effect of India’s Total Sanitation Campaign on Defecation Behaviors and Child Health in Rural Madhya Pradesh: A Cluster Randomized Controlled Trial PLOS Medicine. 2014, 11 (8) e1001709 DOI: 10.1371/journal.pmed.1001709
    20. 20
      Pickering, A. J.; Djebbari, H.; Lopez, C.; Coulibaly, M.; Alzua, M. L. Effect of a community-led sanitation intervention on child diarrhoea and child growth in rural Mali: a cluster-randomised controlled trial Lancet Global Health 2015, 3 (11) e701 e711 DOI: 10.1016/S2214-109X(15)00144-8
    21. 21
      Gyorkos, T. W.; Maheu-Giroux, M.; Blouin, B.; Casapia, M. Impact of Health Education on Soil-Transmitted Helminth Infections in Schoolchildren of the Peruvian Amazon: A Cluster-Randomized Controlled Trial PLoS Neglected Trop. Dis. 2013, 7 (9) e2397 DOI: 10.1371/journal.pntd.0002397
    22. 22
      West, S.; Muñoz, B.; Lynch, M.; Kayongoya, A.; Chilangwa, Z.; Mmbaga, B. B. O.; Taylor, H. R. Impact of face-washing on trachoma in Kongwa, Tanzania Lancet 1995, 345 (8943) 155 158 DOI: 10.1016/S0140-6736(95)90167-1
    23. 23
      Freeman, M. C.; Clasen, T.; Brooker, S. J.; Akoko, D. O.; Rheingans, R. The Impact of a School-Based Hygiene, Water Quality and Sanitation Intervention on Soil-Transmitted Helminth Reinfection: A Cluster-Randomized Trial Am. J. Trop. Med. Hyg. 2013, 89 (5) 875 883 DOI: 10.4269/ajtmh.13-0237
    24. 24
      Colford, J. M. J.; Luby, S. P.; Null, C.; Stewart, C. P. In The WASH Benefits Study: Cluster-Randomized Trials in Bangladesh and Kenya to Measure the Effects of Individual and Combined Water Quality, Sanitation, Handwashing and Nutrition Interventions on Child Growth and Diarrhea ASTHM, Atlanta, GA, 2016; Atlanta, GA, 2016.
    25. 25
      Garn, J. V.; Sclar, G. D.; Freeman, M. C.; Penakalapati, G.; Alexander, K. T.; Brooks, P.; Rehfuess, E. A.; Boisson, S.; Medlicott, K. O.; Clasen, T. F. The impact of sanitation interventions on latrine coverage and latrine use: A systematic review and meta-analysis Int. J. Hyg. Environ. Health 2017, 220 (2, Part B) 329 340 DOI: 10.1016/j.ijheh.2016.10.001
    26. 26
      Kaur, M.; Graham, J.; Eisenberg, J. N. S. Livestock Ownership among Rural Households and Child Morbidity and Mortality: An Analysis of Demographic Health Survey Data from 30 Sub-Saharan African Countries (2005–2015) Am. J. Trop. Med. Hyg. 2017, 96 (3) 741 748 DOI: 10.4269/ajtmh.16-0664
    27. 27
      Odagiri, M.; Schriewer, A.; Daniels, M. E.; Wuertz, S.; Smith, W. A.; Clasen, T.; Schmidt, W.-P.; Jin, Y.; Torondel, B.; Misra, P. R.; Panigrahi, P.; Jenkins, M. W. Human fecal and pathogen exposure pathways in rural Indian villages and the effect of increased latrine coverage Water Res. 2016, 100, 232 244 DOI: 10.1016/j.watres.2016.05.015
    28. 28
      Belongia, E. A.; Chyou, P. H.; Greenlee, R. T.; Perez-Perez, G.; Bibb, W. F.; DeVries, E. O. Diarrhea Incidence and Farm-Related Risk Factors for Escherichia coli O157:H7 and Campylobacter jejuni Antibodies among Rural Children J. Infect. Dis. 2003, 187 (9) 1460 1468 DOI: 10.1086/374622
    29. 29
      Cinquepalmi, V.; Monno, R.; Fumarola, L.; Ventrella, G.; Calia, C.; Greco, M. F.; de Vito, D.; Soleo, L. Environmental Contamination by Dog’s Faeces: A Public Health Problem? Int. J. Environ. Res. Public Health 2013, 10 (1) 72 DOI: 10.3390/ijerph10010072
    30. 30
      Jung, B. K.; Lee, S. E.; Lim, H.; Cho, J.; Kim, D. G.; Song, H.; Kim, M. J.; Shin, E. H.; Chai, J. Y. Toxoplasma gondii B1 gene detection in feces of stray cats around Seoul, Korea and genotype analysis of two laboratory-passaged isolates Korean J. Parasitol. 2015, 53 (3) 259 263 DOI: 10.3347/kjp.2015.53.3.259
    31. 31
      Tobin, M. R.; Goldshear, J. L.; Price, L. B.; Graham, J. P.; Leibler, J. H. A Framework to Reduce Infectious Disease Risk from Urban Poultry in the United States Public Health Rep. 2015, 130 (4) 380 391 DOI: 10.1177/003335491513000417
    32. 32
      Williams, S.; Patel, M.; Markey, P.; Muller, R.; Benedict, S.; Ross, I.; Heuzenroeder, M.; Davos, D.; Cameron, S.; Krause, V. Salmonella in the tropical household environment - Everyday, everywhere J. Infect. 2015, 71 (6) 642 648 DOI: 10.1016/j.jinf.2015.09.011
    33. 33
      Williams, S.; Markey, P.; Harlock, M.; Binns, P.; Gaggin, J.; Patel, M. Individual and household-level risk factors for sporadic salmonellosis in children J. Infect. 2016, 72 (1) 36 44 DOI: 10.1016/j.jinf.2015.09.014
    34. 34
      Headey, D.Newsflash: Chickens don’t use toilets - Why global WASH efforst should start focusing on animal feces. http://www.ifpri.org/blog/newsflash-chickens-dont-use-toilets (accessed 7 February 2017) .
    35. 35
      Moher, D.; Liberati, A.; Tetzlaff, J.; Altman, D. G. The, P. G., Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement PLOS Medicine. 2009, 6 (7) e1000097 DOI: 10.1371/journal.pmed.1000097
    36. 36
      Black, R. E.; Lopez de Romaña, G.; Brown, K. H.; Bravo, N.; Bazalar, O. G.; Kanashiro, H. C. Incidence and etiology of infantile diarrhea and major routes of transmission in Huascar, Peru Am. J. Epidemiol. 1989, 129 (4) 785 799 DOI: 10.1093/oxfordjournals.aje.a115193
    37. 37
      Bukenya, G. B.; Nwokolo, N. Compound hygiene, presence of standpipe and the risk of childhood diarrhoea in an urban settlement of Papua New Guinea International Journal of Epidemiology 1991, 20 (2) 534 539 DOI: 10.1093/ije/20.2.534
    38. 38
      Collinet-Adler, S.; Babji, S.; Sarkar, R.; Kattula, D.; Mohan, V.; Ward, H.; Kang, G.; Balraj, V.; Naumova, E. Environmental indicators of diarrhea in Vellore, India Am. J. Trop. Med. Hyg. 2011, 85 (6) 175
    39. 39
      Grados, O.; Bravo, N.; Black, R. E.; Butzler, J. P. Paediatric campylobacter diarrhoea from household exposure to live chickens in Lima, Peru Bull. World Health Org. 1988, 66 (3) 369 374
    40. 40
      Headey, D.; Nguyen, P.; Kim, S.; Rawat, R.; Ruel, M.; Menon, P. Is Exposure to Animal Feces Harmful to Child Nutrition and Health Outcomes? A Multicountry Observational Analysis Am. J. Trop. Med. Hyg. 2017, 96 (4) 961 969 DOI: 10.4269/ajtmh.16-0270
    41. 41
      Oberhelman, R. A.; Gilman, R. H.; Sheen, P.; Cordova, J.; Zimic, M.; Cabrera, L.; Meza, R.; Perez, J. An Intervention-Control Study of Corraling of Free-Ranging Chickens to Control Campylobacter Infections Among Children in a Peruvian Periurban Shantytown Am. J. Trop. Med. Hyg. 2006, 74 (6) 6
    42. 42
      Adjei, A. A.; Armah, H.; Rodrigues, O.; Renner, L.; Borketey, P.; Ayeh-Kumi, P.; Adiku, T.; Sifah, E.; Lartey, M. Cryptosporidium spp., a frequent cause of diarrhea among children at the Korle-Bu Teaching Hospital, Accra, Ghana Jpn. J. Infect. Dis. 2004, 57 (5) 216 219
    43. 43
      Schmidt, W. P.; Boisson, S.; Routray, P.; Bell, M.; Cameron, M.; Torondel, B.; Clasen, T. Exposure to cows is not associated with diarrhoea or impaired child growth in rural Odisha, India: a cohort study Epidemiol. Infect. 2016, 144 (1) 53 63 DOI: 10.1017/S0950268815001090
    44. 44
      Randremanana, R. V.; Razafindratsimandresy, R.; Andriatahina, T.; Randriamanantena, A.; Ravelomanana, L.; Randrianirina, F.; Richard, V. Etiologies, Risk Factors and Impact of Severe Diarrhea in the Under-Fives in Moramanga and Antananarivo, Madagascar PLoS One 2016, 11 (7) e0158862 DOI: 10.1371/journal.pone.0158862
    45. 45
      Headey, D.; Hirvonen, K. Is Exposure to Poultry Harmful to Child Nutrition? An Observational Analysis for Rural Ethiopia PLoS One 2016, 11 (8) e0160590 DOI: 10.1371/journal.pone.0160590
    46. 46
      Hetherington, J. B.; Wiethoelter, A. K.; Negin, J.; Mor, S. M. Livestock ownership, animal source foods and child nutritional outcomes in seven rural village clusters in Sub-Saharan Africa Agriculture and Food Security 2017, 6 (1) 9 DOI: 10.1186/s40066-016-0079-z
    47. 47
      Mosites, E.; Thumbi, S. M.; Otiang, E.; McElwain, T. F.; Njenga, M. K.; Rabinowitz, P. M.; Rowhani-Rahbar, A.; Neuhouser, M. L.; May, S.; Palmer, G. H.; Walson, J. L. Relations between Household Livestock Ownership, Livestock Disease, and Young Child Growth J. Nutr. 2016, 146 (5) 1118 1124 DOI: 10.3945/jn.115.225961
    48. 48
      George, C. M.; Oldja, L.; Biswas, S. K.; Perin, J.; Lee, G. O.; Ahmed, S.; Haque, R.; Sack, R. B.; Parvin, T.; Azmi, I. J.; Bhuyian, S. I.; Talukder, K. A.; Faruque, A. G. Fecal Markers of Environmental Enteropathy are Associated with Animal Exposure and Caregiver Hygiene in Bangladesh Am. J. Trop. Med. Hyg. 2015, 93 (2) 269 275 DOI: 10.4269/ajtmh.14-0694
    49. 49
      Campbell, D.; Elia, M.; Lunn, P. Growth faltering in rural Gambian infants is associated with impaired small intestinal barrier function, leading to endotoxemia and systematic inflammation J. Nutr. 2003, 133 (5) 1332 1338
    50. 50
      Goto, R.; Mascie-Taylor, C. G. N.; Lunn, P. G. Impact of intestinal permeability, inflammation status and parasitic infections on infant growth faltering in rural Bangladesh Br. J. Nutr. 2009, 101 (10) 1509 1516 DOI: 10.1017/S0007114508083554
    51. 51
      Guerrant, R. L.; Oriá, R. B.; Moore, S. R.; Oriá, M. O. B.; Lima, A. A. M. Malnutrition as an enteric infectious disease with long-term effects on child development Nutr. Rev. 2008, 66 (9) 487 505 DOI: 10.1111/j.1753-4887.2008.00082.x
    52. 52
      Humphrey, J. H. Child undernutrition, tropical enteropathy, toilets, and handwashing Lancet 2009, 374 (9694) 1032 1035 DOI: 10.1016/S0140-6736(09)60950-8
    53. 53
      Lunn, P. G.; Northrop-Clewes, C. A.; Downes, R. M. Intestinal permeability, mucosal injury, and growth faltering in Gambian infants Lancet 1991, 338 (8772) 907 910 DOI: 10.1016/0140-6736(91)91772-M
    54. 54
      Lunn, P. G. Growth retardation and stunting of children in developing countries Br. J. Nutr. 2002, 88 (2) 109 110 DOI: 10.1079/BJN2002652
    55. 55
      Ordiz, M. I.; Shaikh, N.; Trehan, I.; Maleta, K.; Stauber, J.; Shulman, R.; Devaraj, S.; Tarr, P. I.; Manary, M. J. Environmental Enteric Dysfunction is Associated with Poor Linear Growth and Can be Identified by Host Fecal mRNAs J. Pediatr. Gastroenterol. Nutr. 2016, 63 (5) 453 DOI: 10.1097/MPG.0000000000001315
    56. 56
      El-Tras, W. F.; Holt, H. R.; Tayel, A. A.; El-Kady, N. N. Campylobacter infections in children exposed to infected backyard poultry in Egypt Epidemiol. Infect. 2015, 143 (2) 308 315 DOI: 10.1017/S095026881400096X
    57. 57
      Marquis, G. S.; Ventura, G.; Gilman, R. H.; Porras, E.; Miranda, E.; Carbajal, L.; Pentafiel, M. Am. J. Public Health 1990, 80 (2) 146 149 DOI: 10.2105/AJPH.80.2.146
    58. 58
      Vasco, K.; Graham, J. P.; Trueba, G. Detection of Zoonotic Enteropathogens in Children and Domestic Animals in a Semirural Community in Ecuador Appl. Environ. Microbiol. 2016, 82 (14) 4218 4224 DOI: 10.1128/AEM.00795-16
    59. 59
      Moore, C. E.; Elwin, K.; Phot, N.; Seng, C.; Mao, S.; Suy, K.; Kumar, V.; Nader, J.; Bousfield, R.; Perera, S.; Bailey, J. W.; Beeching, N. J.; Day, N. P. J.; Parry, C. M.; Chalmers, R. M. Molecular Characterization of Cryptosporidium Species and Giardia duodenalis from Symptomatic Cambodian Children PLoS Neglected Trop. Dis. 2016, 10 (7) e0004822 DOI: 10.1371/journal.pntd.0004822
    60. 60
      Wanyiri, J. W.; Kanyi, H.; Maina, S.; Wang, D. E.; Steen, A.; Ngugi, P.; Kamau, T.; Waithera, T.; O’Connor, R.; Gachuhi, K.; Wamae, C. N.; Mwamburi, M.; Ward, H. D. Cryptosporidiosis in HIV/AIDS Patients in Kenya: Clinical Features, Epidemiology, Molecular Characterization and Antibody Responses Am. J. Trop. Med. Hyg. 2014, 91 (2) 319 328 DOI: 10.4269/ajtmh.13-0254
    61. 61
      Wumba, R.; Longo-Mbenza, B.; Menotti, J.; Mandina, M.; Kintoki, F.; Situakibanza, N. H.; Kakicha, M. K.; Zanga, J.; Mbanzulu-Makola, K.; Nseka, T.; Mukendi, J. P.; Kendjo, E.; Sala, J.; Thellier, M. Epidemiology, clinical, immune, and molecular profiles of microsporidiosis and cryptosporidiosis among HIV/AIDS patients Int. J. Gen. Med. 2012, 5, 603 611
    62. 62
      Anuar, T. S.; Azreen, S. N.; Salleh, F. M.; Moktar, N. Molecular epidemiology of giardiasis among Orang Asli in Malaysia: application of the triosephosphate isomerase gene BMC Infect. Dis. 2014, 14 (1) 78 DOI: 10.1186/1471-2334-14-78
    63. 63
      Alyousefi, N. A.; Mahdy, M. A.; Mahmud, R.; Lim, Y. A. Factors associated with high prevalence of intestinal protozoan infections among patients in Sana’a City, Yemen PLoS One 2011, 6 (7) e22044 DOI: 10.1371/journal.pone.0022044
    64. 64
      Li, X.-X.; Chen, J.-X.; Wang, L.-X.; Tian, L.-G.; Zhang, Y.-P.; Dong, S.-P.; Hu, X.-G.; Liu, J.; Wang, F.-F.; Wang, Y.; Yin, X.-M.; He, L.-J.; Yan, Q.-Y.; Zhang, H.-W.; Xu, B.-L.; Zhou, X.-N. Prevalence and risk factors of intestinal protozoan and helminth infections among pulmonary tuberculosis patients without HIV infection in a rural county in P. R. China Acta Trop. 2015, 149, 19 26 DOI: 10.1016/j.actatropica.2015.05.001
    65. 65
      Bern, C.; Kawai, V.; Vargas, D.; Rabke-Verani, J.; Williamson, J.; Chavez-Valdez, R.; Xiao, L.; Sulaiman, I.; Vivar, A.; Ticona, E.; Ñavincopa, M.; Cama, V.; Moura, H.; Secor, W.; Visvesvara, G.; Gilman, R. H. The Epidemiology of Intestinal Microsporidiosis in Patients with HIV/AIDS in Lima, Peru J. Infect. Dis. 2005, 191 (10) 1658 1664 DOI: 10.1086/429674
    66. 66
      Dwivedi, K. K.; Prasad, G.; Saini, S.; Mahajan, S.; Lal, S.; Baveja, U. K. Enteric Opportunistic Parasites among HIV Infected Individuals: Associated Risk Factors and Immune Status Jpn. J. Infect. Dis. 2007, 60, 76 81
    67. 67
      Bublitz, D. C.; Wright, P. C.; Bodager, J. R.; Rasambainarivo, F. T.; Bliska, J. B.; Gillespie, T. R. Epidemiology of Pathogenic Enterobacteria in Humans, Livestock, and Peridomestic Rodents in Rural Madagascar PLoS One 2014, 9 (7) e101456 DOI: 10.1371/journal.pone.0101456
    68. 68
      Leung, D.; Das, S.; Malek, M.; Ahmed, D.; Khanam, F.; Qadri, F.; Faruque, A.; Ryan, E. Non-typhoidal Salmonella gastroenteritis at a diarrheal hospital in Dhaka, Bangladesh, 1996–2011 Am. J. Trop. Med. Hyg. 2013, 88 (4) 661 669 DOI: 10.4269/ajtmh.12-0672
    69. 69
      Labrique, A. B.; Zaman, K.; Hossain, Z.; Saha, P.; Yunus, M.; Hossain, A.; Ticehurst, J.; Kmush, B.; Nelson, K. E. An Exploratory Case Control Study of Risk Factors for Hepatitis E in Rural Bangladesh PLoS One 2013, 8 (5) e61351 DOI: 10.1371/journal.pone.0061351
    70. 70
      Mpyet, C.; Lass, B. D.; Yahaya, H. B.; Solomon, A. W. Prevalence of and Risk Factors for Trachoma in Kano State, Nigeria PLoS One 2012, 7 (7) e40421 DOI: 10.1371/journal.pone.0040421
    71. 71
      Nigusie, A.; Berhe, R.; Gedefaw, M. Prevalence and associated factors of active trachoma among childeren aged 1–9 years in rural communities of Gonji Kolella district, West Gojjam zone, North West Ethiopia BMC Res. Notes 2015, 8 (1) 641 DOI: 10.1186/s13104-015-1529-6
    72. 72
      Cumberland, P.; Hailu, G.; Todd, J. Active trachoma in children aged three to nine years in rural communities in Ethiopia: prevalence, indicators and risk factors Trans. R. Soc. Trop. Med. Hyg. 2005, 99 (2) 120 127 DOI: 10.1016/j.trstmh.2004.03.011
    73. 73
      Reichert, F.; Pilger, D.; Schuster, A.; Lesshafft, H.; Guedes de Oliveira, S.; Ignatius, R.; Feldmeier, H. Prevalence and Risk Factors of Hookworm-Related Cutaneous Larva Migrans (HrCLM) in a Resource-Poor Community in Manaus, Brazil PLoS Neglected Trop. Dis. 2016, 10 (3) e0004514 DOI: 10.1371/journal.pntd.0004514
    74. 74
      Acosta-Jamett, G.; Weitzel, T.; Boufana, B.; Adones, C.; Bahamonde, A.; Abarca, K.; Craig, P. S.; Reiter-Owona, I. Prevalence and risk factors for echinococcal infection in a rural area of northern Chile: A household-based cross-sectional study PLoS Neglected Trop. Dis. 2014, 8 (8) 1 9 DOI: 10.1371/journal.pntd.0003090
    75. 75
      Chiodo, P.; Basualdo, J.; Ciarmela, L.; Pezzani, B.; Apezteguía, M.; Minvielle, M. Related factors to human toxocariasis in a rural community of Argentina Memorias do Instituto Oswaldo Cruz. 2006, 101 (4) 397 400 DOI: 10.1590/S0074-02762006000400009
    76. 76
      Fernando, S.; Wickramasinghe, V.; Kapilananda, G.; Devasurendra, R.; Amarasooriya, J.; Dayaratne, H. Epidemiological aspects and risk factors of Toxocariasis in pediatric population in Sri Lanka Southeast Asian J. Trop. Med. Public Health 2007, 38 (6) 983 990
    77. 77
      Subrata, I. M.; Suryadhi, N. T.; Mantik-Astawa, N.; Damriyasa, I. M. Epidemiological and molecular analysis of Taxoplasa gondii in faecal samples of house cats obtained from house of maternal in Bali Bali Medical Journal 2015, 4 (2) 68 75 DOI: 10.15562/bmj.v4i2.122
    78. 78
      Daniels, M. E.; Shrivastava, A.; Smith, W. A.; Sahu, P.; Odagiri, M.; Misra, P. R.; Panigrahi, P.; Suar, M.; Clasen, T.; Jenkins, M. W. Cryptosporidium and giardia in humans, domestic animals, and village water sources in rural India Am. J. Trop. Med. Hyg. 2015, 93 (3) 596 600 DOI: 10.4269/ajtmh.15-0111
    79. 79
      Schriewer, A.; Odagiri, M.; Wuertz, S.; Misra, P. R.; Panigrahi, P.; Clasen, T.; Jenkins, M. W. Human and animal fecal contamination of community water sources, stored drinking water and hands in rural India measured with validated microbial source tracking assays Am. J. Trop. Med. Hyg. 2015, 93 (3) 509 516 DOI: 10.4269/ajtmh.14-0824
    80. 80
      Daniels, M. E.; Smith, W. A.; Schmidt, W. P.; Clasen, T.; Jenkins, M. W. Modeling Cryptosporidium and Giardia in Ground and Surface Water Sources in Rural India: Associations with Latrines, Livestock, Damaged Wells, and Rainfall Patterns Environ. Sci. Technol. 2016, 50 (14) 7498 7507 DOI: 10.1021/acs.est.5b05797
    81. 81
      Lupindu, A. M.; Olsen, J. E.; Ngowi, H. A.; Msoffe, P. L. M.; Mtambo, M. M.; Scheutz, F.; Dalsgaard, A. Occurrence and characterization of Shiga toxin-producing Escherichia coli O157:H7 and other non-sorbitol-fermenting E. coli in cattle and humans in urban areas of Morogoro, Tanzania Vector-Borne and Zoonotic Diseases. 2014, 14 (7) 503 510 DOI: 10.1089/vbz.2013.1502
    82. 82
      Nyariki, D. M.; Mwang’ombe, A. W.; Thompson, D. M. Land-use change and livestock production challenges in an integrated system: the Masai-Mara ecosystem, Kenya J. Hum. Ecol. 2009, 26 (3) 11
    83. 83
      Wolking, D. J.; Clifford, D. L.; Kelly, T. R.; Kamani, E.; Smith, W. A.; Kazwala, R. R.; Mazet, J. A. K. Boma to banda - a disease sentinel concept for reduction of diarrhoea Pastoralism: Research, Policy and Practice 2016, 6 (1) 13 DOI: 10.1186/s13570-016-0059-8
    84. 84
      Sprenger, L. K.; Green, K. T.; Molento, M. B. Geohelminth contamination of public areas and epidemiological risk factors in Curitiba, Brazil Rev. Bras. Parasitol. Vet. 2014, 23 (1) 69 73 DOI: 10.1590/S1984-29612014009
    85. 85
      Tun, S.; Ithoi, I.; Mahmud, R.; Samsudin, N. I.; Heng, C. K.; Ling, L. Y. Detection of Helminth Eggs and Identification of Hookworm Species in Stray Cats, Dogs and Soil from Klang Valley, Malaysia PLoS One 2015, 10 (12) e0142231 DOI: 10.1371/journal.pone.0142231
    86. 86
      Boehm, A. B.; Wang, D.; Ercumen, A.; Shea, M.; Harris, A. R.; Shanks, O. C.; Kelty, C.; Ahmed, A.; Mahmud, Z. H.; Arnold, B. F.; Chase, C.; Kullmann, C.; Colford, J. M.; Luby, S. P.; Pickering, A. J. Occurrence of Host-Associated Fecal Markers on Child Hands, Household Soil, and Drinking Water in Rural Bangladeshi Households Environ. Sci. Technol. Lett. 2016, 3 (11) 393 398 DOI: 10.1021/acs.estlett.6b00382
    87. 87
      Harris, A. R.; Pickering, A. J.; Harris, M.; Doza, S.; Islam, M. S.; Unicomb, L.; Luby, S.; Davis, J.; Boehm, A. B. Ruminants Contribute Fecal Contamination to the Urban Household Environment in Dhaka, Bangladesh Environ. Sci. Technol. 2016, 50 (9) 4642 DOI: 10.1021/acs.est.5b06282
    88. 88
      Ngure, F. M.; Humphrey, J. H.; Mbuya, M. N. N.; Majo, F.; Mutasa, K.; Govha, M.; Mazarura, E.; Chasekwa, B.; Prendergast, A. J.; Curtis, V.; Boor, K. J.; Stoltzfus, R. J. Formative Research on Hygiene Behaviors and Geophagy among Infants and Young Children and Implications of Exposure to Fecal Bacteria Am. J. Trop. Med. Hyg. 2013, 89 (4) 709 716 DOI: 10.4269/ajtmh.12-0568
    89. 89
      Sultana, R.; Nahar, N.; Rimi, N. A.; Azad, S.; Islam, M. S.; Gurley, E. S.; Luby, S. P. Backyard poultry raising in Bangladesh: a valued resource for the villagers and a setting for zoonotic transmission of avian influenza. A qualitative study Rural and Remote Health 2012, 12 (1927) 1 14
    90. 90
      Uga, S.; Hoa, N. T.; Noda, S.; Moji, K.; Cong, L.; Aoki, Y.; Rai, S. K.; Fujimaki, Y. Parasite egg contamination of vegetables from a suburban market in Hanoi, Vietnam Nepal Med. College J. 2009, 11 (2) 75 78
    91. 91
      Scallan, E.; Hoekstra, R. M.; Angulo, F. J.; Tauxe, R. V.; Widdowson, M.-A.; Roy, S. L.; Jones, J. L.; Griffin, P. M. Foodborne Illness Acquired in the United States—Major Pathogens Emerging Infect. Dis. 2011, 17 (1) 7 15 DOI: 10.3201/eid1701.P11101
    92. 92
      a Mpalang, R. K.; Boreux, R.; Melin, P.; Akir Ni Bitiang, K.; Daube, G.; De Mol, P. Prevalence of Campylobacter among goats and retail goat meat in Congo J. Infect. Dev. Countries 2014, 8 (2) 168 175 DOI: 10.3855/jidc.3199
    93. 93
      Osbjer, K.; Boqvist, S.; Sokerya, S.; Kannarath, C.; San, S.; Davun, H.; Magnusson, U. Household practices related to disease transmission between animals and humans in rural Cambodia BMC Public Health 2015, 15 (1) 476 DOI: 10.1186/s12889-015-1811-5
    94. 94
      Anuar, T. S.; Sarhan Al-Mekhlafi, H. M.; Abdul Ghani, M. K.; Moktar, N. Prevalence and risk factors associated with Entamoeba histolytica/Entamoeba dispar/Entamoeba moshkovskii complex infection among different tribes of Malaysian aborigines Int. J. Infect. Dis. 2012, 16, e175 e176 DOI: 10.1016/j.ijid.2012.05.725
    95. 95
      Suwannarong, K.; Chapman, R. S. Characteristics associated with contact with rodents in, around, and outside homes in Khon Kaen Province, Thailand Am. J. Trop. Med. Hyg. 2015, 92 (4) 784 790 DOI: 10.4269/ajtmh.14-0195
    96. 96
      Vujcic, J.; Ram, P. K.; Hussain, F.; Unicomb, L.; Gope, P. S.; Abedin, J.; Mahmud, Z. H.; Sirajul Islam, M.; Luby, S. P. Toys and toilets: cross-sectional study using children’s toys to evaluate environmental faecal contamination in rural Bangladeshi households with different sanitation facilities and practices Trop. Med. Int. Health 2014, 19 (5) 528 536 DOI: 10.1111/tmi.12292
    97. 97
      Torondel, B.; Gyekye-Aboagye, Y.; Routray, P.; Boisson, S.; Schimdt, W.; Clasen, T. Laboratory development and field testing of sentinel toys to assess environmental faecal exposure of young children in rural India Trans. R. Soc. Trop. Med. Hyg. 2015, 109 (6) 386 392 DOI: 10.1093/trstmh/trv023
    98. 98
      Harvey, S. A.; Winch, P. J.; Leontsini, E.; Torres Gayoso, C.; López Romero, S.; Gilman, R. H.; Oberhelman, R. A. Domestic poultry-raising practices in a Peruvian shantytown: implications for control of Campylobacter jejuni-associated diarrhea Acta Trop. 2003, 86 (1) 41 54 DOI: 10.1016/S0001-706X(03)00006-8
    99. 99
      Arnold, B. F.; Null, C.; Luby, S. P.; Unicomb, L.; Stewart, C. P.; Dewey, K. G.; Ahmed, T.; Ashraf, S.; Christensen, G.; Clasen, T.; Dentz, H. N.; Fernald, L. C. H.; Haque, R.; Hubbard, A. E.; Kariger, P.; Leontsini, E.; Lin, A.; Njenga, S. M.; Pickering, A. J.; Ram, P. K.; Tofail, F.; Winch, P. J.; Colford, J. M. Cluster-randomised controlled trials of individual and combined water, sanitation, hygiene and nutritional interventions in rural Bangladesh and Kenya: the WASH Benefits study design and rationale BMJ. Open 2013, 3 (8) e003476 DOI: 10.1136/bmjopen-2013-003476
    100. 100
      Hussain, F. Continued household faecal contamination following a sanitation intervention in rural Bangladesh. Health Sci. Bull. 2013, 11 (1), 9–14 (En), 9–14 (Bengali).
    101. 101

      Sanitation Hygiene Infant Nutrition Efficacy

      Trial, T.; Humphrey, J. H.; Jones, A. D.; Manges, A.; Mangwadu, G.; Maluccio, J. A.; Mbuya, M. N.; Moulton, L. H.; Ntozini, R.; Prendergast, A. J.; Stoltzfus, R. J.; Tielsch, J. M. The Sanitation Hygiene Infant Nutrition Efficacy (SHINE) Trial: Rationale, Design, and Methods Clin. Infect. Dis. 2015, 61 (Suppl 7) S685 702
    102. 102
      Hall, D.; Alam, M. G. S.; Raha, S. K. Reducing risk of emerging infectious diseases in Bangladesh through ecohealth Int. J. Infect. Dis. 2012, 16, e38 DOI: 10.1016/j.ijid.2012.05.096
    103. 103
      Cassenote, A. J. F.; de Abreu Lima, A. R.; Pinto Neto, J. M.; Rubinsky-Elefant, G. Seroprevalence and Modifiable Risk Factors for Toxocara spp. in Brazilian Schoolchildren PLoS Neglected Trop. Dis. 2014, 8 (5) e2830 DOI: 10.1371/journal.pntd.0002830
    104. 104
      Smolders, A.; Rolls, R. J.; Ryder, D.; Watkinson, A.; Mackenzie, M. Cattle-derived microbial input to source water catchments: An experimental assessment of stream crossing modification J. Environ. Manage. 2015, 156, 143 149 DOI: 10.1016/j.jenvman.2015.03.052
    105. 105
      Harwood, V. J.; Staley, C.; Badgley, B. D.; Borges, K.; Korajkic, A. Microbial source tracking markers for detection of fecal contamination in environmental waters: relationships between pathogens and human health outcomes FEMS Microbiology Reviews. 2014, 38 (1) 1 40 DOI: 10.1111/1574-6976.12031
    106. 106
      Liu, J.; Gratz, J.; Amour, C.; Kibiki, G.; Becker, S.; Janaki, L.; Verweij, J. J.; Taniuchi, M.; Sobuz, S. U.; Haque, R.; Haverstick, D. M.; Houpt, E. R. A Laboratory-Developed TaqMan Array Card for Simultaneous Detection of 19 Enteropathogens Journal of Clinical Microbiology 2013, 51 (2) 472 480 DOI: 10.1128/JCM.02658-12
    107. 107
      Platts-Mills, J. A.; Babji, S.; Bodhidatta, L.; Gratz, J.; Haque, R.; Havt, A.; McCormick, B. J. J.; McGrath, M.; Olortegui, M. P.; Samie, A.; Shakoor, S.; Mondal, D.; Lima, I. F. N.; Hariraju, D.; Rayamajhi, B. B.; Qureshi, S.; Kabir, F.; Yori, P. P.; Mufamadi, B.; Amour, C.; Carreon, J. D.; Richard, S. A.; Lang, D.; Bessong, P.; Mduma, E.; Ahmed, T.; Lima, A. A. A. M.; Mason, C. J.; Zaidi, A. K. M.; Bhutta, Z. A.; Kosek, M.; Guerrant, R. L.; Gottlieb, M.; Miller, M.; Kang, G.; Houpt, E. R. Pathogen-specific burdens of community diarrhoea in developing countries: a multisite birth cohort study (MAL-ED) Lancet Global Health 2015, 3 (9) e564 e575 DOI: 10.1016/S2214-109X(15)00151-5
    108. 108
      McLellan, S. L.; Eren, A. M. Discovering new indicators of fecal pollution Trends Microbiol. 2014, 22 (12) 697 706 DOI: 10.1016/j.tim.2014.08.002
    109. 109
      McLeroy, K. R.; Bibeau, D.; Steckler, A.; Glanz, K. An Ecological Perspective on Health Promotion Programs Health Education Quarterly. 1988, 15 (4) 351 377 DOI: 10.1177/109019818801500401
    110. 110
      Mupawaenda, A. C.; Chawatama, S.; Muvavarirwa, P. Gender issues in livestock production: a case study of Zimbabwe Trop. Anim. Health Prod. 2009, 41 (7) 1017 DOI: 10.1007/s11250-008-9268-5
    111. 111
      WHO; UNICEF. WASH Post-2015: Proposed indicatorsfor drinkingwater, sanitation, and hygiene. WHO/UNICEF Joint Monitoring Programmefor Water Supply and Sanitation, Geneca. (2015.
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    Supporting Information


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    • Further details about methods including full search string and databases used, global PRISMA chart, data extraction form, PRISMA checklist, and table of study characteristics (PDF)


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