Affiliation:
1. Unité des Agents Antibactériens, Institut Pasteur, 75724 Paris Cedex 15
2. Centre d'Etudes Pharmaceutiques, Châtenay-Malabry, France
Abstract
ABSTRACT
We have identified a second resistance-nodulation-cell division (RND)-type efflux pump, AdeIJK, in clinical isolate
Acinetobacter baumannii
BM4454. The
adeI, adeJ
, and
adeK
genes encode, respectively, the membrane fusion, RND, and outer membrane components of the pump. AdeJ belongs to the AcrB protein family (57% identity with AcrB from
Escherichia coli
). mRNA analysis by Northern blotting and reverse transcription-PCR indicated that the genes were cotranscribed. Overexpression of the cloned
adeIJK
operon was toxic in both
E. coli
and
Acinetobacter
. The
adeIJK
genes were detected in all of the 60 strains of
A. baumannii
tested. The two latter observations suggest that the AdeIJK complex might contribute to intrinsic but not to acquired antibiotic resistance in
Acinetobacter
. To characterize the substrate specificity of the pump, we have constructed derivatives of BM4454 in which
adeIJK
(strain BM4579),
adeABC
(strain BM4561), or both groups of genes (strain BM4652) were inactivated by deletion-insertion. Determination of the antibiotic susceptibility of these strains and of BM4652 and BM4579, in which the
adeIJK
operon was provided in
trans
, indicated that the AdeIJK pump contributes to resistance to β-lactams, chloramphenicol, tetracycline, erythromycin, lincosamides, fluoroquinolones, fusidic acid, novobiocin, rifampin, trimethoprim, acridine, safranin, pyronine, and sodium dodecyl sulfate. The chemical structure of these molecules suggests that amphiphilic compounds are the preferred substrates. The AdeABC and AdeIJK efflux systems contributed in a more than additive fashion to tigecycline resistance.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
302 articles.
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