Affiliation:
1. Unité des Agents Antibactériens, Institut Pasteur, Paris
2. Centre d'Etudes Pharmaceutiques, ChÂtenay-Malabry, France
Abstract
ABSTRACT
The AdeABC pump of
Acinetobacter baumannii
BM4454, which confers resistance to various antibiotic classes including aminoglycosides, is composed of the AdeA, AdeB, and AdeC proteins; AdeB is a member of the RND superfamily. The
adeA
,
adeB
, and
adeC
genes are contiguous and adjacent to
adeS
and
adeR
, which are transcribed in the opposite direction and which specify proteins homologous to sensors and regulators of two-component systems, respectively (S. Magnet, P. Courvalin, and T. Lambert, Antimicrob. Agents Chemother. 45:3375-3380, 2001). Analysis by Northern hybridization indicated that the three genes were cotranscribed, although mRNAs corresponding to
adeAB
and
adeC
were also present. Cotranscription of the two regulatory genes was demonstrated by reverse transcription-PCR. Inactivation of
adeS
led to aminoglycoside susceptibility. Transcripts corresponding to
adeAB
were not detected in susceptible
A. baumannii
CIP 70-10 but were present in spontaneous gentamicin-resistant mutants obtained in vitro. Analysis of these mutants revealed the substitutions Thr153→Met in AdeS downstream from the putative His-149 site of autophosphorylation, which is presumably responsible for the loss of phosphorylase activity by the sensor, and Pro116→Leu in AdeR at the first residue of the α
5
helix of the receiver domain, which is involved in interactions that control the output domain of response regulators. These mutations led to constitutive expression of the pump and, thus, to antibiotic resistance. These data indicate that the AdeABC pump is cryptic in wild
A. baumannii
due to stringent control by the AdeRS two-component system.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
325 articles.
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