Teo Jeanette Woon Pei, Ng Kah Ying, Lin Raymond Tzer Pin
Department of Laboratory Medicine, National University Hospital, Singapore, Singapore.
Int J Antimicrob Agents. 2009 Feb;33(2):177-80. doi: 10.1016/j.ijantimicag.2008.08.019. Epub 2008 Nov 6.
Polymerase chain reaction (PCR) screening of 116 ciprofloxacin-resistant Klebsiella pneumoniae hospital isolates for the presence of qnr genes that mediate plasmid quinolone resistance revealed that none were positive for qnrA or qnrS. However, qnrB was detected in ca. 5.2% of the isolates. Southern hybridisation demonstrated that the qnrB-hybridising plasmids were large (>70kb) and capable of transferring quinolone resistance by conjugation. Sequence analysis of the qnrB genes detected in this study showed that they were identical to previously identified qnrB1, qnrB4 and qnrB6 genes, although a novel variant designated qnrB20 was also identified. Analysis of the genetic environment around the cloned qnrB genes showed that they were present in diverse plasmid backbones, sometimes within novel genetic contexts, but always associated with mobile or transposable elements.
对116株耐环丙沙星的肺炎克雷伯菌医院分离株进行聚合酶链反应(PCR)筛查,以检测介导质粒喹诺酮耐药性的qnr基因的存在,结果显示没有一株qnrA或qnrS呈阳性。然而,约5.2%的分离株中检测到了qnrB。Southern杂交表明,与qnrB杂交的质粒很大(>70kb),并且能够通过接合转移喹诺酮耐药性。本研究中检测到的qnrB基因的序列分析表明,它们与先前鉴定的qnrB1、qnrB4和qnrB6基因相同,不过还鉴定出了一个新的变体qnrB20。对克隆的qnrB基因周围的遗传环境分析表明,它们存在于不同的质粒骨架中,有时处于新的遗传背景下,但总是与移动或转座元件相关。