Marchand Isabelle, Damier-Piolle Laurence, Courvalin Patrice, Lambert Thierry
Unité des Agents Antibactériens, Institut Pasteur, 25, rue du Docteur Roux, 75724 Paris Cedex 15, France.
Antimicrob Agents Chemother. 2004 Sep;48(9):3298-304. doi: 10.1128/AAC.48.9.3298-3304.2004.
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 alpha(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.
鲍曼不动杆菌BM4454的AdeABC泵可赋予对包括氨基糖苷类在内的多种抗生素的抗性,它由AdeA、AdeB和AdeC蛋白组成;AdeB是RND超家族的成员。adeA、adeB和adeC基因相邻,且与adeS和adeR相邻,adeS和adeR以相反方向转录,分别编码与双组分系统的传感器和调节子同源的蛋白质(S. Magnet、P. Courvalin和T. Lambert,《抗菌剂与化疗》45:3375 - 3380,2001)。Northern杂交分析表明这三个基因是共转录的,不过也存在对应adeAB和adeC的mRNA。逆转录 - PCR证明了两个调节基因的共转录。adeS的失活导致对氨基糖苷类敏感。在敏感的鲍曼不动杆菌CIP 70 - 10中未检测到对应adeAB的转录本,但在体外获得的自发庆大霉素抗性突变体中存在。对这些突变体的分析揭示,在假定的自磷酸化His - 149位点下游的AdeS中发生了Thr153→Met替换,这可能是传感器磷酸化酶活性丧失的原因,在接收域α(5)螺旋的第一个残基处的AdeR中发生了Pro116→Leu替换,该残基参与控制反应调节子输出域的相互作用。这些突变导致泵的组成型表达,从而导致抗生素抗性。这些数据表明,由于AdeRS双组分系统的严格控制,AdeABC泵在野生鲍曼不动杆菌中是隐性的。