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Identification of mtDNA Lineages of Sus scrofa by Multiplex Single Base Extension for the Authentication of Processed Food Products

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Instituto de Patologia e Imunologia da Universidade do Porto (IPATIMUP), Rua Dr. Roberto Frias s/n, 4200-465 Porto, Portugal
Faculdade de Ciências, Universidade do Porto, Rua do Campo Alegre s/n, 4169-007 Porto, Portugal
E-mail: [email protected]. Phone: +351225570700. Fax: +351225570799.
Cite this: J. Agric. Food Chem. 2011, 59, 13, 6920–6926
Publication Date (Web):June 14, 2011
https://doi.org/10.1021/jf201283r
Copyright © 2011 American Chemical Society
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Abstract

A genetic method to identify the breed of origin could serve as a useful tool for inspecting the authenticity of the increasing number of monobreed foodstuffs, such as those derived from small local European pig breeds. Mitochondrial DNA (mtDNA) is practically the only reliable genomic target for PCR in processed products, and its haploid nature and strict maternal inheritance greatly facilitate genetic analysis. As a result of strategies that sought to improve the production traits of European pigs, most industrial breeds presently show a high frequency of Asian alleles, while the absence or low frequency of such Asian alleles has been observed in small rustic breeds from which highly prized dry-cured and other traditional products are derived. Therefore, the detection of Asian ancestry would indicate nonconformity in Protected Denomination of Origin products. This study presents a single base extension assay based on 15 diagnostic mtDNA single nucleotide polymorphisms to discriminate between Asian and European Sus scrofa lineages. The test was robust, sensitive and accurate in a wide range of processed foodstuffs and allowed accurate detection of pig genetic material and identification of maternal ancestry. A market survey suggested that nonconformity of products derived from Portuguese breeds is an unusual event at present, but regular surveys both in the local populations and in commercial products would be advisible. Taking into consideration the limitations presented by other methodologies, this mtDNA-based test probably attains the highest resolution for the direct genetic test for population of origin in Sus scrofa food products.

Supporting Information

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Additional PCR data, list of test products and phylogenetic identifications, partial overview of the alignment of 48 complete Asian and European mitochondrial Sus scrofa sequences, and maximum likelihood phylogenetic tree including 63 Sus scrofa mitochondrial control region sequences. This material is available free of charge via the Internet at http://pubs.acs.org.

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Cited By


This article is cited by 5 publications.

  1. Julie T. Millard, Edward Chuang, James S. Lucas, Erzsebet E. Nagy, and Griffin T. Davis . Case-Study Investigation of Equine Maternity via PCR-RFLP: A Biochemistry Laboratory Experiment. Journal of Chemical Education 2013, 90 (11) , 1518-1521. https://doi.org/10.1021/ed300740r
  2. Jane M. Caldwell. Food Analysis Using Organelle DNA and the Effects of Processing on Assays. Annual Review of Food Science and Technology 2017, 8 (1) , 57-74. https://doi.org/10.1146/annurev-food-030216-030216
  3. E. Maestri, N. Marmiroli. Advances in Polymerase Chain Reaction Technologies for Food Authenticity Testing. 2016,,, 285-309. https://doi.org/10.1016/B978-0-08-100220-9.00011-4
  4. Silvia Portarena, Enrico Brugnoli. Traceability and Authenticity of Dietary Lipids. 2016,,, 223-248. https://doi.org/10.1016/B978-1-78242-247-1.00009-0
  5. Rosangela Marchelli, Tullia Tedeschi, Alessandro Tonelli. DNA Analyses in Food Safety and Quality: Current Status and Expectations. 2012,,, 25-63. https://doi.org/10.1007/978-94-007-1226-3_2

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