首页 | 本学科首页   官方微博 | 高级检索  
     

广州地区产CTX-M型超广谱β内酰胺酶大肠埃希菌和肺炎克雷伯菌的研究
引用本文:卓超,苏丹虹,李红玉,王露霞,廖康,王媚,植志全,郭仲辉,魏衍超,耿穗娜,金光耀,钟南山. 广州地区产CTX-M型超广谱β内酰胺酶大肠埃希菌和肺炎克雷伯菌的研究[J]. 中华检验医学杂志, 2009, 32(10). DOI: 10.3760/cma.j.issn.1009-9158.2009.10.007
作者姓名:卓超  苏丹虹  李红玉  王露霞  廖康  王媚  植志全  郭仲辉  魏衍超  耿穗娜  金光耀  钟南山
作者单位:1. 广州医学院,呼吸疾病国家重点实验室,510120
2. 中山大学附属第二医院
3. 广州军区广州总医院
4. 中山大学附属第一医院
5. 广东省人民医院
6. 广州花都区人民医院
7. 广州番禺区人民医院
8. 广州医学院第二附属医院
9. 南方医科大学南方医院
基金项目:广州市科技局重点攻关项目 
摘    要:目的 研究广州地区大肠埃希菌和肺炎克雷伯菌CTX-M型超广谱β内酰胺酶(ESBLs)的分子表型、流行病学和耐药基因环境特征.方法 收集2007-2008年广州地区9家医院临床分离产ESBLs的181株大肠埃希菌和180株肺炎克雷伯菌,通过PCR检测ESBLs分子表型;通过接合试验、质粒图谱、PCR分析CTX-M-15型ESBLs的基因环境,肠杆菌科基因间重复序列引物PCR(ERIC-PCR)分析产CTX-M-15型ESBLs菌株的分子同源性.结果 67.3%(243/361)的ESBLs产生株为CTX-M表型,其中CTX-M-1群和CTX-M-9群各占46.9%(114/243)和53.1%(129/243),未发现其他CTX-M亚群.CTX-M-14和CTXM-15是最常见的ESBLs基因型,其中CTX-M-14在大肠埃希菌和肺炎克雷伯菌的检出率分别35.4%(64/181)和28.3%(51/180),CTX-M-15在这两种菌的检出率分别为21.5%(39/181)和26.1%(47/180),此外还检出对头孢他啶有水解活性的CTX-M-55、CTX-M-19和CTX-M-27.采用ERIC-PER分析CTX-M-15产生株的同源性,39株大肠埃希菌被分为28个基因型,47株肺炎克雷伯菌被分为30个基因型.67.6%(25/37)和32.4%(12/37)bla_(CTX-M-15)分别位于65 000 bp和90 000 bp的可接合质粒上,65 000 bp质粒除bla_(CTX-M-15)阳性外,未检到bla_(TEM-1)、qnrB、bla_(DHA-1)、bla_(OXA-1),aac(6′)-I6-cr等耐药基因.1株接合菌90 000 bp质粒还存在bla_(OXA-1)和bla_(TEM-1)耐药基因,其余7个90 000 bp质粒所携耐药基因同65 000 bp质粒.所有bla_(CTX-M-15)都位于ISEcp1-like插入序列下游,ISEep1-like末端与blaCTX-M-15间距均为48 bp.结论 广州地区ESBLs主要分子表型为CTX-M型主要流行为CTX-M-14型.以CTX-M-15为代表能水解头孢他啶的CTX-M型ESBLs在本地区检出增多值得关注.

关 键 词:大肠杆菌  克雷伯菌  肺炎  β内酰胺酶类  大肠杆菌蛋白质类  表型  微生物敏感性试验  聚合酶链反应

Study on CIX-M type ESBLs-producing Escherichia coli and Klebsiella pneumoiae in Guangzhou
ZHUO Chao,SU Dan-hong,LI Hong-yu,WANG Lu-xia,LIAO Kang,WANG Mei,ZHI Zhi-quan,GUO Zhong-hui,WEI Yan-chao,GENG Sui-na,JIN Guang-yao,ZHONG Nan-shan. Study on CIX-M type ESBLs-producing Escherichia coli and Klebsiella pneumoiae in Guangzhou[J]. Chinese Journal of Laboratory Medicine, 2009, 32(10). DOI: 10.3760/cma.j.issn.1009-9158.2009.10.007
Authors:ZHUO Chao  SU Dan-hong  LI Hong-yu  WANG Lu-xia  LIAO Kang  WANG Mei  ZHI Zhi-quan  GUO Zhong-hui  WEI Yan-chao  GENG Sui-na  JIN Guang-yao  ZHONG Nan-shan
Abstract:Objective To study phylogenies, epidemiology and genetic environment of CTX-M type of ESBLs produced by Escherichia coli and Klebsiella pneumoniae isolated from nine hospitals in Guangzhou. Methods The phylogenies of CTX-M type of ESBLs were analyzed by PCR Genetic environment of CTX-M-15 encoding gene (bla_(CTX-M-15)) were investigated by conjugation test and plasmid analysis. The clonal relationship of strains producing CTX-M-15 was determined by enterobacterial repetitive intergenic consensus PCR (ERIC-PCR). Results A total of 361 ESBLs-producing isolates of Escherichia coli and Klebsiella pneumoniae were collected. 67.3% of ESBLs strains were detected to produce CTX-M-type ESBLs, and the commonest genotypes in Escherichia coli and Klebsiella pneumoniae were CTX-M-14 (35.4% and 28.3%), CTX-M-15(21.5% and 26.1%) EBIC-PCR products of all CTX-M-15-producing strains show 39 strains of Escherichia coli were classified into 27 genotypes while 43 strains of Klebsiella pneumoniae were divided into 30 genotypes. Furthermore, the genotypes of CTX-M-55, CTX-M-19, CTX-M-27, with ceftazidime-hydrelyzing activity, were detected in this study. The great majority of bla_(CTX-M-15) genes were found to locate on a 65 000 bp-conjugative plasmid, and there was no blaTEM-1, bla_(OXA-1), blaDSA-1 or aac (6')-Ib-cr gene coexisted on the plasmid, ISEcp1-like insertion sequences, relative to mobilization of bla_(CTX-M-15) gene, were detected in all bla_(CTX-M-15) positive strains, and the distances between the end of ISEcp1-like insertion sequences and the start cedon of bla_(CTX-M-15) were equal, with 48 base pairs. Conclusion CTX-M-14 is still the most common genotype of ESBLs in Guangzhou, but high prevalence of CTX-M-15 ESBLs hydrolyzing ceftazidime already appears in south China.
Keywords:Escherichia coli  Klebsiella pneumoniae  beta-Lactamases  Escherichia coli proteins  Phenotype  Micrebiol sensitivity tests  Polymerase chain reaction
本文献已被 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号