Affiliation:
1. Laboratoire de Bactériologie, Hôpital Jean Minjoz, Besançon
2. Laboratoire de Bactériologie Médicale, Hôpital du Bocage, Dijon, France
Abstract
ABSTRACT
Simultaneous overexpression of the MexAB-OprM and MexXY efflux systems was demonstrated by real-time reverse transcription-PCR and immunoblotting experiments for 12 multiresistant clinical isolates of
Pseudomonas aeruginosa
. DNA sequencing analysis showed that nine of these strains (named
agrZ
mutants) harbored mutations in
mexZ
, the product of which downregulates the expression of the
mexXY
operon. In addition, 8 of the 12 strains exhibited mutations in genes known to control transcription of the
mexAB-oprM
operon. Four of them were
nalB
mutants with alterations in the repressor gene
mexR
, three of them appeared to be
nalC
mutants deficient in gene
PA3721
and overexpressing gene
PA3720
, and one strain was a
nalB nalC
double mutant. For MexAB-OprM as well as for MexXY, no clear correlation could be established between (i) the types of mutations, (ii) the expression level of
mexA
or
mexX
, and (iii) resistance to effluxed antibiotics. Finally, three isolates, named
agrW
mutants, overproduced MexXY and had an intact
mexZ
gene, and four strains overproduced MexAB-OprM and had intact
mexR
and
PA3721
genes (
nalD
mutants). These data show that clinical isolates are able to broaden their drug resistance profiles by coexpressing two Mex efflux pumps and suggest the existence of additional regulators for MexAB-OprM and MexXY.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
217 articles.
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