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肺炎克雷伯菌的喹诺酮外排基因qepA的检测及菌株同源性分析
引用本文:马晓波,林粼,宋秀宇,房丽丽,张加勤,郑港森,郑燕青. 肺炎克雷伯菌的喹诺酮外排基因qepA的检测及菌株同源性分析[J]. 中华微生物学和免疫学杂志, 2011, 31(1). DOI: 10.3760/cma.j.issn.0254-5101.2011.01.012
作者姓名:马晓波  林粼  宋秀宇  房丽丽  张加勤  郑港森  郑燕青
作者单位:1. 厦门大学附属第一医院检验科,361003
2. 厦门大学附属第一医院中心实验室,361003
摘    要:目的 检测质粒介导的喹诺酮类外排基因qepA在临床分离的产超广谱β-内酰胺酶(ESBLs)的肺炎克雷伯菌中的分布情况,并对阳性菌株进行同源性分析.方法 41株细菌的鉴定和药敏采用Vitek-2 Compact系统;采用PCR法检测qepA并进行序列测定、比对.应用Rep-PCR法采用Diversilab系统对qepA阳性菌株进行同源性分析;同时了解阳性株上的rmtB分布情况.结果 5株肺炎克雷伯菌上检测到qepA基因,检出率为12.2%.Diversilab分析结果表明其中两株的qepA阳性菌同源性超过99%.包含qepA的肺炎克雷伯菌中2株(40%)检出rmtB.结论 在肺炎克雷伯菌临床菌株上检出质粒介导的喹诺酮类外排基因qepA.
Abstract:
Objective To investigate the prevalence of qepA, quinolone efflux protein, among 41 unique clinical strains of K. pneumoniae producing ESBLs and to study the qepA-bearing isolates using the Diversilab system. Methods Identification and antimicrobial susceptibility were performed by Vitek-2 Compact System. Screening of qepA was carried out by PCR amplification. The NCBI BLAST program was utilized for sequence comparisons. qnr-bearing strains was evaluated by the Repetitive-sequence-based PCR(Rep-PCR) employing the Diversilab system. And the existence of rmtB was detected among these qepA contained isolates. Results qepA were detected in 5 isolates( 12.2% ). The Rep-PCR profiles produced by the Diversilab system showed that 2/5 of isolates were indistinguishable. And 60% of qepA-positive isolates were detected to harbor rmtB gene. Conclusion The data suggest the emergence of qepA-borne K. pneumoniae.

关 键 词:质粒介导  肺炎克雷伯菌

Study of qepA among clinical isolates of Klebsialla pneumoniae
MA Xiao-bo,LIN Lin,SONG Xiu-yu,FANG Li-li,ZHANG Jia-qin,ZHENG Gang-sen,ZHENG Yan-qing. Study of qepA among clinical isolates of Klebsialla pneumoniae[J]. Chinese Journal of Microbiology and Immunology, 2011, 31(1). DOI: 10.3760/cma.j.issn.0254-5101.2011.01.012
Authors:MA Xiao-bo  LIN Lin  SONG Xiu-yu  FANG Li-li  ZHANG Jia-qin  ZHENG Gang-sen  ZHENG Yan-qing
Abstract:Objective To investigate the prevalence of qepA, quinolone efflux protein, among 41 unique clinical strains of K. pneumoniae producing ESBLs and to study the qepA-bearing isolates using the Diversilab system. Methods Identification and antimicrobial susceptibility were performed by Vitek-2 Compact System. Screening of qepA was carried out by PCR amplification. The NCBI BLAST program was utilized for sequence comparisons. qnr-bearing strains was evaluated by the Repetitive-sequence-based PCR(Rep-PCR) employing the Diversilab system. And the existence of rmtB was detected among these qepA contained isolates. Results qepA were detected in 5 isolates( 12.2% ). The Rep-PCR profiles produced by the Diversilab system showed that 2/5 of isolates were indistinguishable. And 60% of qepA-positive isolates were detected to harbor rmtB gene. Conclusion The data suggest the emergence of qepA-borne K. pneumoniae.
Keywords:qepA
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