The Two-Component System Bacillus Respiratory Response A and B (BrrA−BrrB) Is a Virulence Factor Regulator in Bacillus anthracis

Sara M. Vetter and Patrick M. Schlievert*
Department of Microbiology, University of Minnesota Medical School, Minneapolis, Minnesota 55455
Biochemistry, 2007, 46 (25), pp 7343–7352
DOI: 10.1021/bi700184s
Publication Date (Web): May 31, 2007
Copyright © 2007 American Chemical Society

 This work was supported by USPHS Research Grant AI057164 from the National Institute of Allergy and Infectious Diseases and a grant from the Great Lakes Regional Center of Excellence in Biodefense and Emerging Infectious Diseases. S.M.V. is supported by a graduate student fellowship from the American Society for Microbiology.

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*

 To whom correspondence should be addressed. E-mail:  schli001@ umn.edu.

Abstract

Abstract Image

Bacillus anthracis, a bioterrorism threat as well as an agricultural concern, has complex mechanisms for regulation of its major virulence factors. Genome searches identified the putative two-component system that we designated Bacillus anthracis respiratory response (Brr)A−BrrB. A brrA deletion strain was constructed, and real-time reverse transcriptase polymerase chain reaction and Western blot analysis were used to assess the effect of BrrA−BrrB on levels of virulence factors, the regulator atxA, and growth characteristics. When brrA was deleted, the genes for anthrax toxins (lethal factor, protective antigen, and edema factor) where expressed 4−6-log10-fold less than in the parent Sterne strain. The global regulator atxA was downregulated when compared to atxA in the Sterne strain. Thus, the BrrA−BrrB two-component system positively regulates B. anthracis toxin genes as well as the atxA regulator. Aerobic growth was not affected by the ΔbrrA mutation, but colonies showed differences in morphology, the mutant did not sporulate, and the strain lost the ability to synthesize cytochrome aa3. Gel-shift mobility assays demonstrated that BrrA bound to the promoters of genes for both protective antigen and cytochrome aa3, demonstrating that BrrA is a transcription factor. BrrA−BrrB has sequence similarity with the virulence regulator SrrA−SrrB in Staphylococcus aureus and the aerobic/anaerobic regulator, ResD−ResE, in B. subtilis, and appears to share regulatory mechanisms with ResD−ResE.

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History

  • Published In Issue June 26, 2007
  • Received January 29, 2007
    Revised Manuscript Received April 10, 2007

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