Affiliation:
1. Department of Microbiology and Immunology, Queen's University, Kingston, Ontario, Canada K7L 3N6
Abstract
ABSTRACT
Exposure to reactive oxygen species (ROS) (e.g., peroxide) was shown to induce expression of the PA5471 gene, which was previously shown to be required for antimicrobial induction of the MexXY components of the MexXY-OprM multidrug efflux system and aminoglycoside resistance determinant in
Pseudomonas aeruginosa. mexXY
was also induced by peroxide exposure, and this too was PA5471 dependent. The prospect of ROS promoting
mexXY
expression and aminoglycoside resistance recalls
P. aeruginosa
infection of the chronically inflamed lungs of cystic fibrosis (CF) patients, where the organism is exposed to ROS and where MexXY-OprM predominates as the mechanism of aminoglycoside resistance. While ROS did not enhance aminoglycoside resistance
in vitro
, long-term (8-day) exposure of
P. aeruginosa
to peroxide (mimicking chronic
in vivo
ROS exposure) increased aminoglycoside resistance frequency, dependent upon PA5471 and
mexXY
. This enhanced resistance frequency was also seen in a mutant strain overexpressing PA5471, in the absence of peroxide, suggesting that induction of PA5471 by peroxide was key to peroxide enhancement of aminoglycoside resistance frequency. Resistant mutants selected following peroxide exposure were typically pan-aminoglycoside-resistant, with
mexXY
generally required for this resistance. Moreover, PA5471 was required for
mexXY
expression and aminoglycoside resistance in these as well as several CF isolates examined.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
99 articles.
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