JAC Advance Access published online on September 1, 2003
Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkg390
© 2003 by The British Society for Antimicrobial Chemotherapy
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Brief report
1 Department of Microbiology, Faculty of Pharmaceutical Sciences,
Okayama University, Tsushima, Okayama, 700-8530, Japan
* Corresponding author. E-mail: tsuchiya{at}pharm.okayama-u.ac.jp.
Received 30 April 2003
; revised 19 June 2003
; accepted 25 June 2003
Objectives: Multidrug efflux pumps
are thought to be involved in mediating multidrug resistance in Pseudomonas aeruginosa. Here we aim to characterize
hitherto uncharacterized multidrug efflux pumps from
P. aeruginosa. Materials and methods: We isolated a mutant,
YM442, which showed elevated resistance to several antimicrobial
agents from P. aeruginosa YM44 lacking four major
multidrug efflux pumps, MexAB, MexCD-OprJ, MexEF-OprN
and MexXY. We cloned genes responsible for the resistance from chromosomal
DNA of YM442 using YM44 as host. Results: We designated the genes mexVW.
Introduction of a recombinant plasmid pTAJ2 carrying the mexVW into
YM44 cells conferred resistance to fluoroquinolones, tetracycline,
chloramphenicol, erythromycin, ethidium bromide and acriflavine.
Elevated ethidium bromide extrusion was observed with cells of YM442
and of YM44/pTAJ2. An outer membrane protein OprM was able to cooperate
with MexVW. Elevated expression of the mexV gene
was observed with YM442 compared with YM44. Conclusions: MexV (membrane fusion protein)-MexW
(RND-type membrane protein)-OprM is a tripartite multidrug
efflux pump. It is suggested that other outer membrane component(s)
could cooperate with MexVW.
Keywords: MexVW, multidrug efflux pump, RND-type, P.
aeruginosa
A new member of the tripartite multidrug efflux
pumps,
MexVW-OprM, in Pseudomonas aeruginosa
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