Smith Lisa K, Mankin Alexander S
Center for Pharmaceutical Biotechnology, m/c 870, University of Illinois, 900 S. Ashland Ave., Chicago, IL 60607, USA.
Antimicrob Agents Chemother. 2008 May;52(5):1703-12. doi: 10.1128/AAC.01583-07. Epub 2008 Feb 25.
The methyltransferase genes erm(B) and cfr are adjacent to each other in the chromosome of methicillin-resistant Staphylococcus aureus strain CM05. Analyses of the transcriptional organization of the erm(B) and cfr genes in the chromosome of strain CM05 showed that the two genes are organized into an operon, designated mlr (for modification of the large ribosomal subunit), which is controlled by the erm(B) promoter. Analysis of the translation control and the inducibility of the erm(B) and cfr genes in the mlr operon showed that despite the presence of putative regulatory short open reading frames, both genes are expressed constitutively. The combined action of the two methyltransferases encoded in the mlr operon results in modification of two specific residues in 23S rRNA, A2058 and A2503, and renders cells resistant to all clinically useful antibiotics that target the large ribosomal subunit. Furthermore, simultaneous modification of both rRNA sites synergistically enhances resistance to 16-member-ring macrolides.
在耐甲氧西林金黄色葡萄球菌菌株CM05的染色体中,甲基转移酶基因erm(B)和cfr彼此相邻。对菌株CM05染色体中erm(B)和cfr基因转录组织的分析表明,这两个基因被组织成一个操纵子,命名为mlr(用于修饰大核糖体亚基),它由erm(B)启动子控制。对mlr操纵子中erm(B)和cfr基因的翻译控制及诱导性分析表明,尽管存在假定的调控性短开放阅读框,但这两个基因都是组成型表达的。mlr操纵子中编码的两种甲基转移酶的联合作用导致23S rRNA中的两个特定残基A2058和A2503发生修饰,并使细胞对所有靶向大核糖体亚基的临床有用抗生素产生抗性。此外,两个rRNA位点的同时修饰协同增强了对16元环大环内酯类抗生素的抗性。