Affiliation:
1. Department of Microbiology and Immunology, Dartmouth Medical School, Hanover, New Hampshire 03755
Abstract
ABSTRACT
MgrA is a pleiotropic regulator that controls autolysis, virulence, and efflux pump activity in
Staphylococcus aureus
. We recently found that
mgrA
mutants of strains RN6390, SH1000, and MW2 also displayed enhanced biofilm formation compared with their respective parents. The biofilms formed by
mgrA
mutants of RN6390 and MW2 are independent of
sigB
and
ica
loci, two genetic elements that have been previously associated with biofilm formation in
S. aureus
. Biofilms formed by
mgrA
mutants are dependent on the expression of surface proteins mediated by the sortase gene
srtA
. Extracellular DNA was also a crucial component of the early biofilm of
mgrA
mutants. Genetic analysis indicated that biofilm formation in
mgrA
mutants is mediated in part by
agr
RNAIII, a genetic locus regulated by
mgrA
. Additionally, SarA is important to biofilm formation in
mgrA
mutants since the double
sarA mgrA
mutants failed to form biofilms compared to single
mgrA
mutants of RN6390 and MW2. However, the SarA-mediated effect is independent of
agr
and proteases such as V8 protease and aureolysin. Collectively, our data showed MgrA to be a repressor of biofilm formation, and biofilms formed by
mgrA
mutants have features that are distinct from other reported biofilm types in
S. aureus
.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
83 articles.
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