Affiliation:
1. Microbiology Group, Department of Biological Sciences, Illinois State University, Normal, Illinois 61790-4120
Abstract
ABSTRACT
Genome-wide transcriptional profiling studies of the response of
Staphylococcus aureus
to cell wall-active antibiotics have led to the discovery of a cell wall stress stimulon of genes induced by these agents.
msrA1
, encoding methionine sulfoxide reductase, is a highly induced member gene of this stimulon. In the present study we show that
msrA1
induction by oxacillin is common to all methicillin-susceptible strains studied but did not occur in two homogeneous and two heterogeneous methicillin-resistant strains. However,
msrA1
was induced by vancomycin and/or
d
-cycloserine in methicillin-resistant strains. Lysozyme and lysostaphin treatment did not induce
msrA1
expression. Oxacillin-induced
msrA1
expression was enhanced by ca. 30% in a SigB
+
derivative (SH1000) of the SigB-defective RN450 (NCTC 8325-4) strain.
msrA1
expression was not affected in mutants in the global regulatory systems
agr
and
sar
. Glycerol monolaurate, an inhibitor of signal transduction, inhibited the oxacillin-induced transcription of
msrA1
and other cell wall stress stimulon member genes,
vraS
and
dnaK
. These observations suggest that the cell wall stress stimulon is induced by inhibition of the process of peptidoglycan biosynthesis, and the inhibitory effects of glycerol monolaurate indicate that gene expression is dependent on a signal transduction pathway.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
35 articles.
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