Affiliation:
1. Harvard Medical School and Brigham and Women's Hospital, Department of Medicine, Channing Laboratory, and HHMI, 181 Longwood Ave., Boston Massachusetts, 02115
Abstract
ABSTRACT
The Cpx two-component system is thought to mediate envelope stress responses in many gram-negative bacteria and has been implicated in the pathogenicity of several enteric pathogens. While cues that activate the
Escherichia coli
Cpx system have been identified, the nature of the molecular signals that stimulate this pathway is not well understood. Here, we investigated stimuli that trigger this system in
Vibrio cholerae
, a facultative pathogen that adapts to various niches during its life cycle. In contrast to
E. coli
, there was no basal activity of the
V. cholerae
Cpx pathway under standard laboratory conditions. Furthermore, several known stimuli of the
E. coli
pathway did not induce expression of this system in
V. cholerae
. There were no defects in intestinal growth in
V
.
cholerae cpx
mutants, arguing against the idea that this pathway promotes
V
.
cholerae
adaptation to conditions in the mammalian host. We discovered that chloride ions activate the
V. cholerae
Cpx pathway, raising the possibility that this signal transduction system provides a means for
V. cholerae
to sense and respond to alterations in salinity. We used a genetic approach to screen for mutants in which the Cpx pathway is activated. We found that mutations in genes whose products are required for periplasmic disulfide bond isomerization result in activation of the Cpx pathway, suggesting that periplasmic accumulation of proteins with aberrant disulfide bonds triggers the
V. cholerae
Cpx pathway.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
38 articles.
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