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Role of Vibrio polysaccharide (vps) genes in VPS production, biofilm formation and Vibrio cholerae pathogenesis
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Biofilm formation enhances the survival and persistence of the facultative human pathogen
Vibrio cholerae
in natural ecosystems and its transmission during seasonal cholera outbreaks. A major component of the
V. cholerae
biofilm matrix is the
Vibrio
polysaccharide (VPS), which is essential for development of three-dimensional biofilm structures. The
vps
genes are clustered in two regions, the
vps-
I cluster (
vpsU
,
vpsA–K
, VC0916–27) and the
vps-
II cluster (
vpsL–Q
, VC0934–39), separated by an intergenic region containing the
rbm
gene cluster that encodes biofilm matrix proteins. In-frame deletions of the
vps
clusters and genes encoding matrix proteins drastically altered biofilm formation phenotypes. To determine which genes within the
vps
gene clusters are required for biofilm formation and VPS synthesis, we generated in-frame deletion mutants for all the
vps
genes. Many of these mutants exhibited reduced capacity to produce VPS and biofilms. Infant mouse colonization assays revealed that mutants lacking either
vps
clusters or
rbmA
(encoding secreted matrix protein RbmA) exhibited a defect in intestinal colonization compared to the wild-type. Understanding the roles of the various
vps
gene products will aid in the biochemical characterization of the VPS biosynthetic pathway and elucidate how
vps
gene products contribute to VPS biosynthesis, biofilm formation and virulence in
V. cholerae
.
Microbiology Society
Title: Role of Vibrio polysaccharide (vps) genes in VPS production, biofilm formation and Vibrio cholerae pathogenesis
Description:
Biofilm formation enhances the survival and persistence of the facultative human pathogen
Vibrio cholerae
in natural ecosystems and its transmission during seasonal cholera outbreaks.
A major component of the
V.
cholerae
biofilm matrix is the
Vibrio
polysaccharide (VPS), which is essential for development of three-dimensional biofilm structures.
The
vps
genes are clustered in two regions, the
vps-
I cluster (
vpsU
,
vpsA–K
, VC0916–27) and the
vps-
II cluster (
vpsL–Q
, VC0934–39), separated by an intergenic region containing the
rbm
gene cluster that encodes biofilm matrix proteins.
In-frame deletions of the
vps
clusters and genes encoding matrix proteins drastically altered biofilm formation phenotypes.
To determine which genes within the
vps
gene clusters are required for biofilm formation and VPS synthesis, we generated in-frame deletion mutants for all the
vps
genes.
Many of these mutants exhibited reduced capacity to produce VPS and biofilms.
Infant mouse colonization assays revealed that mutants lacking either
vps
clusters or
rbmA
(encoding secreted matrix protein RbmA) exhibited a defect in intestinal colonization compared to the wild-type.
Understanding the roles of the various
vps
gene products will aid in the biochemical characterization of the VPS biosynthetic pathway and elucidate how
vps
gene products contribute to VPS biosynthesis, biofilm formation and virulence in
V.
cholerae
.
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