Affiliation:
1. Department of Laboratory Medicine & Pathobiology, Faculty of Medicine, University of Toronto, Toronto, Canada
2. Division of Clinical Integrative Biology, Sunnybrook Health Sciences Centre, 2075 Bayview Avenue, S1-26A, Toronto, Ontario, Canada, M4N 3N5
Abstract
ABSTRACT
As an etiological agent of bacterial sepsis and wound infections,
Vibrio vulnificus
is unique among the
Vibrionaceae
. Its continued environmental persistence and transmission are bolstered by its ability to colonize shellfish, form biofilms on various marine biotic surfaces, and generate a morphologically and physiologically distinct rugose (R) variant that yields profuse biofilms. Here, we identify a c-di-GMP-regulated locus (
brp
, for
b
iofilm and
r
ugose
p
olysaccharide) and two transcription factors (BrpR and BrpT) that regulate these physiological responses. Disruption of glycosyltransferases within the locus or either regulator abated the inducing effect of c-di-GMP on biofilm formation, rugosity, and stress resistance. The same lesions, or depletion of intracellular c-di-GMP levels, abrogated these phenotypes in the R variant. The parental and
brp
mutant strains formed only scant monolayers on glass surfaces and oyster shells, and although the R variant formed expansive biofilms, these were of limited depth. Dramatic vertical expansion of the biofilm structure was observed in the parental strain and R variant, but not the
brp
mutants, when intracellular c-di-GMP levels were elevated. Hence, the
brp
-encoded polysaccharide is important for surface colonization and stress resistance in
V. vulnificus
, and its expression may control how the bacteria switch from a planktonic lifestyle to colonizing shellfish to invading human tissue.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
39 articles.
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