Affiliation:
1. Department of Microbiology and Immunology, Stanford University Medical School, Stanford, California 94305-5428
Abstract
ABSTRACT
Vibrio cholerae
is known to persist in aquatic environments under nutrient-limiting conditions. To analyze the possible involvement of the alternative sigma factor encoded by
rpoS
, which is shown to be important for survival during nutrient deprivation in several other bacterial species, a
V. cholerae rpoS
homolog was cloned by functional complementation of an
Escherichia coli
mutant by using a wild-type genomic library. Sequence analysis of the complementing clone revealed an 1.008-bp open reading frame which is predicted to encode a 336-amino-acid protein with 71 to 63% overall identity to other reported
rpoS
gene products. To determine the functional role of
rpoS
in
V. cholerae
, we inactivated
rpoS
by homologous recombination.
V. cholerae
strains lacking
rpoS
are impaired in the ability to survive diverse environmental stresses, including exposure to hydrogen peroxide, hyperosmolarity, and carbon starvation. These results suggest that
rpoS
may be required for the persistence of
V. cholerae
in aquatic habitats. In addition, the
rpoS
mutation led to reduced production or secretion of hemagglutinin/protease. However,
rpoS
is not critical for in vivo survival, as determined by an infant mouse intestinal competition assay.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
206 articles.
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