Jayol Aurélie, Nordmann Patrice, Brink Adrian, Poirel Laurent
Medical and Molecular Microbiology "Emerging Antibiotic Resistance" Unit, Department of Medicine, Faculty of Science, University of Fribourg, Fribourg, Switzerland.
Medical and Molecular Microbiology "Emerging Antibiotic Resistance" Unit, Department of Medicine, Faculty of Science, University of Fribourg, Fribourg, Switzerland HFR-Hôpital Cantonal de Fribourg, Fribourg, Switzerland.
Antimicrob Agents Chemother. 2015 May;59(5):2780-4. doi: 10.1128/AAC.05055-14. Epub 2015 Mar 2.
A multidrug-resistant Klebsiella pneumoniae isolate exhibiting heteroresistance to colistin was investigated. The colistin-resistant subpopulation harbored a single amino acid change (Asp191Tyr) in protein PhoP, which is part of the PhoPQ two-component system that activates pmrHFIJKLM expression responsible for l-aminoarabinose synthesis and polymyxin resistance. Complementation assays with a wild-type phoP gene restored full susceptibility to colistin. Then, analysis of the colistin-susceptible subpopulation showed a partial deletion (25 bp) in the phoP gene compared to that in the colistin-resistant subpopulation. That deletion disrupted the reading frame of phoP, leading to a longer and inactive protein (255 versus 223 amino acids long). This is the first report showing the involvement of mutation(s) in PhoP in colistin resistance. Furthermore, this is the first study to decipher the mechanisms leading to colistin heteroresistance in K. pneumoniae.
对一株对黏菌素表现出异质性耐药的多重耐药肺炎克雷伯菌分离株进行了研究。耐黏菌素亚群在PhoP蛋白中存在单个氨基酸变化(Asp191Tyr),PhoP是PhoPQ双组分系统的一部分,该系统激活负责L-阿拉伯糖合成和多粘菌素耐药性的pmrHFIJKLM表达。用野生型phoP基因进行互补试验可恢复对黏菌素的完全敏感性。然后,对黏菌素敏感亚群的分析显示,与耐黏菌素亚群相比,phoP基因存在部分缺失(25 bp)。该缺失破坏了phoP的阅读框,导致产生更长且无活性的蛋白质(分别为255个和223个氨基酸长)。这是首次报道PhoP中的突变与黏菌素耐药性有关。此外,这是首次对肺炎克雷伯菌中导致黏菌素异质性耐药的机制进行解析的研究。