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Bicarbonate increases binding affinity of Vibrio cholerae ToxT to virulence gene promoters.

Abstract
The major Vibrio cholerae virulence gene transcription activator, ToxT, is responsible for the production of the diarrhea-inducing cholera toxin (CT) and the major colonization factor, toxin coregulated pilus (TCP). In addition to the two primary virulence factors mentioned, ToxT is responsible for the activation of accessory virulence genes, such as aldA, tagA, acfA, acfD, tcpI, and tarAB. ToxT activity is negatively modulated by bile and unsaturated fatty acids found in the upper small intestine. Conversely, previous work identified another intestinal signal, bicarbonate, which enhances the ability of ToxT to activate production of CT and TCP. The work presented here further elucidates the mechanism for the enhancement of ToxT activity by bicarbonate. Bicarbonate was found to increase the activation of ToxT-dependent accessory virulence promoters in addition to those that produce CT and TCP. Bicarbonate is taken up into the V. cholerae cell, where it positively affects ToxT activity by increasing DNA binding affinity for the virulence gene promoters that ToxT activates regardless of toxbox configuration. The increase in ToxT binding affinity in the presence of bicarbonate explains the elevated level of virulence gene transcription.
AuthorsJoshua J Thomson, Jeffrey H Withey
JournalJournal of bacteriology (J Bacteriol) Vol. 196 Issue 22 Pg. 3872-80 (Nov 2014) ISSN: 1098-5530 [Electronic] United States
PMID25182489 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2014, American Society for Microbiology. All Rights Reserved.
Chemical References
  • Bacterial Proteins
  • Bicarbonates
  • Transcription Factors
  • tcpN protein, Vibrio cholerae
Topics
  • Bacterial Proteins (genetics, metabolism)
  • Bicarbonates (pharmacology)
  • Gene Expression Regulation, Bacterial (drug effects)
  • Promoter Regions, Genetic
  • Protein Binding
  • Transcription Factors (genetics, metabolism)
  • Vibrio cholerae (drug effects, genetics, metabolism, pathogenicity)
  • Virulence

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