Affiliation:
1. The John D. Dingell Department of Veteran's Affairs Medical Center
2. the Department of Internal Medicine, Division of Infectious Diseases, Wayne State University School of Medicine, Detroit, Michigan
Abstract
ABSTRACT
NorA is a
Staphylococcus aureus
multidrug transporter that confers resistance to structurally distinct compounds. The MgrA global regulatory protein is reported to augment
norA
expression when
mgrA
is overexpressed from an undefined plasmid-based promoter. Further details about
norA
regulatory mechanisms are scant. A chromosomal
norA
::
lacZ
transcriptional fusion was constructed in different
S. aureus
strains, and allele replacement was used to define the relevance of promoter region sequences to
norA
expression. The effect of
mgrA
overexpression in wild-type and mutant backgrounds was also determined. Contrary to existing data, overexpression of
mgrA
repressed
norA
transcription in all parent and selected
norA
promoter mutant strains in a dose-dependent fashion. Disruption of a near-perfect inverted repeat or other putative regulatory protein binding sites did not affect
norA
transcription, but the repressive effect of
mgrA
overexpression was blunted in these mutants. This result, and the conservation of all of these motifs in
S. aureus
, suggests that their presence is required for the full effect of MgrA, or other regulatory proteins, on
norA
expression. Mutations at the +5 nucleotide of
norA
mRNA (
flqB
mutations) had a major impact; all resulted in markedly increased
norA
expression that was significantly reversed by
mgrA
overexpression. The
flqB
position of
norA
mRNA is part of a conserved imperfect inverted repeat; it is feasible that this motif could be a binding site for a
norA
regulatory protein.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
74 articles.
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