Affiliation:
1. State Key Laboratory of Protein and Plant Gene Research,School of Life Sciences, Peking University , Beijing, China
Abstract
ABSTRACT
Pseudomonas aeruginosa
easily produces drug-resistant mutants. A large number of mutational resistome genes exist in the genome of
P. aeruginosa
. In this study, whole genome sequencing analysis of a multidrug-resistant
P. aeruginosa
strain isolated by
in vitro
antibiotic treatment showed a mutation in the
cpxS
gene. Random mutagenesis of
cpxS
was conducted and introduced into the PA14Δ
cpxS
strain. Numerous CpxS mutants, including 14 different single amino acid substitutions, were identified, which led to reduced antibiotic susceptibility. Moreover, some of them were also present in the published genomes of
P. aeruginosa
isolates. Around
cpxS
, a gene coding for a putative sensor kinase, the nearest gene coding for a response regulator is
cpxR
in the genome of
P. aeruginosa
. Deletion of
cpxR
restored antibiotic susceptibility in the above
cpxS
mutant strains. As an extension of our previous work, where the expression of the
mexAB-oprM
operon is directly activated by CpxR in
P. aeruginosa
, in this study, we showed that the expression of the
mexA
promoter was increased in the above
cpxS
mutant strains in a
cpxR
-dependent manner, and
mexA
is prerequisite for the reduced antibiotic susceptibility. Therefore, we propose that the putative sensor kinase CpxS, together with CpxR, comprises a two-component regulatory system regulating the expression of the
mexAB-oprM
operon in
P. aeruginosa
. Our work indicates that
cpxS
, as a novel member of mutational resistome, plays important roles on the development of multidrug resistance in
P. aeruginosa
.
Funder
MOST | National Natural Science Foundation of China
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
2 articles.
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