Affiliation:
1. Division of Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts 02114,1 and
2. Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts 021152
Abstract
ABSTRACT
ToxT, a member of the AraC family of transcriptional regulators, controls the expression of several virulence factors in
Vibrio cholerae
. In the classical biotype of
V. cholerae
, expression of
toxT
is regulated by the same environmental conditions that control expression of the virulence determinants cholera toxin and the toxin coregulated pilus. Several genes that activate
toxT
expression have been identified. To identify genes that repress
toxT
expression in nonpermissive environmental conditions, a genetic screen was used to isolate mutations which alter the expression of a
toxT-gusA
transcriptional fusion. Several mutants were isolated, and the mutants could be divided into two classes. One class of mutants exhibited higher expression levels of
toxT-gusA
at both the nonpermissive pH and temperature, while the second class showed elevated
toxT-gusA
expression only at the nonpermissive pH. One mutant from the second class was chosen for further characterization. This mutant was found to carry a Tn
phoA
insertion in a homolog of the
Escherichia coli pepA
gene. Disruption of
pepA
in
V. cholerae
resulted in elevated levels of expression of cholera toxin,
tcpA
,
toxT
, and
tcpP
at the noninducing pH but not at the noninducing temperature. Elevated levels of expression of
toxT
and
tcpP
at the nonpermissive pH in the
pepA
mutant were abolished in
tcpP toxR
mutant and
aphB
mutant backgrounds, respectively. A putative binding site for PepA was identified in the
tcpPH-tcpI
intergenic region, suggesting that PepA may act at the level of
tcpPH
transcription. Disruption of
pepA
caused only partial deregulation at the noninducing pH, suggesting the involvement of additional factors in the pH regulation of virulence genes in
V. cholerae
.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
62 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献