This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental material
Right arrow An erratum has been published
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Google Scholar
Right arrow Articles by Abuaita, B. H.
Right arrow Articles by Withey, J. H.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Abuaita, B. H.
Right arrow Articles by Withey, J. H.

 Previous Article  |  Next Article 

Infection and Immunity, September 2009, p. 4111-4120, Vol. 77, No. 9
0019-9567/09/$08.00+0     doi:10.1128/IAI.00409-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Bicarbonate Induces Vibrio cholerae Virulence Gene Expression by Enhancing ToxT Activity{triangledown} ,{dagger}

Basel H. Abuaita and Jeffrey H. Withey*

Department of Immunology and Microbiology, Wayne State University School of Medicine, Detroit, Michigan 48201

Received 13 April 2009/ Returned for modification 2 June 2009/ Accepted 20 June 2009

Vibrio cholerae is a gram-negative bacterium that is the causative agent of cholera, a severe diarrheal illness. The two biotypes of V. cholerae O1 capable of causing cholera, classical and El Tor, require different in vitro growth conditions for induction of virulence gene expression. Growth under the inducing conditions or infection of a host initiates a complex regulatory cascade that results in production of ToxT, a regulatory protein that directly activates transcription of the genes encoding cholera toxin (CT), toxin-coregulated pilus (TCP), and other virulence genes. Previous studies have shown that sodium bicarbonate induces CT expression in the V. cholerae El Tor biotype. However, the mechanism for bicarbonate-mediated CT induction has not been defined. In this study, we demonstrate that bicarbonate stimulates virulence gene expression by enhancing ToxT activity. Both the classical and El Tor biotypes produce inactive ToxT protein when they are cultured statically in the absence of bicarbonate. Addition of bicarbonate to the culture medium does not affect ToxT production but causes a significant increase in CT and TCP expression in both biotypes. Ethoxyzolamide, a potent carbonic anhydrase inhibitor, inhibits bicarbonate-mediated virulence induction, suggesting that conversion of CO2 into bicarbonate by carbonic anhydrase plays a role in virulence induction. Thus, bicarbonate is the first positive effector for ToxT activity to be identified. Given that bicarbonate is present at high concentration in the upper small intestine where V. cholerae colonizes, bicarbonate is likely an important chemical stimulus that V. cholerae senses and that induces virulence during the natural course of infection.


* Corresponding author. Mailing address: 540 E. Canfield, Detroit, MI 48201. Phone: (313) 577-1316. Fax: (313) 577-1155. E-mail: jwithey{at}med.wayne.edu

{triangledown} Published ahead of print on 29 June 2009.

{dagger} Supplemental material for this article may be found at http://iai.asm.org/.

Editor: A. Camilli


Infection and Immunity, September 2009, p. 4111-4120, Vol. 77, No. 9
0019-9567/09/$08.00+0     doi:10.1128/IAI.00409-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.