Affiliation:
1. Department of Genetics and Microbiology, Centre Médical Universitaire, Geneva, Switzerland
Abstract
ABSTRACT
We investigated the regulation of the MexEF-OprN multidrug efflux system of
Pseudomonas aeruginosa
, which is overexpressed in
nfxC
-type mutants and confers resistance to quinolones, chloramphenicol and trimethoprim. Sequencing of the DNA region upstream of the
mexEF-oprN
operon revealed the presence of an open reading frame (ORF) of 304 amino acids encoding a LysR-type transcriptional activator, termed MexT. By using T7-polymerase, a 34-kDa protein was expressed in
Escherichia coli
from a plasmid carrying the
mexT
gene. Expression of a
mexE
::
lacZ
fusion was 10-fold higher in
nfxC
-type mutants than in the wild-type strain; however, transcription of
mexT
as well as the
mexT
DNA region was unchanged. Located adjacent to
mexT
but transcribed in opposite direction, the beginning of an ORF termed
qrh
(quinone oxidoreductase homologue) was identified. Expression of a
qrh
::
lacZ
fusion was also found to be activated by MexT. Further, we present evidence for coregulation at the transcriptional and the posttranscriptional level between the MexEF-OprN efflux system and the OprD porin responsible for cross-resistance of
nfxC
-type mutants to carbapenem antibiotics.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
225 articles.
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