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产超广谱β内酰胺酶临床分离株可转移多重耐药分子机制的研究
引用本文:陆坚,唐英春,吴本权,张扣兴,张天托,毕筱刚,朱家馨,谈淑卿.产超广谱β内酰胺酶临床分离株可转移多重耐药分子机制的研究[J].中华结核和呼吸杂志,2003,26(4):199-202.
作者姓名:陆坚  唐英春  吴本权  张扣兴  张天托  毕筱刚  朱家馨  谈淑卿
作者单位:1. 深圳市东湖医院
2. 510630,广州,中山大学附属第三医院呼吸内科
基金项目:广东省科委重点攻关基金资助项目 ( 199810 )
摘    要:目的 研究产超广谱β内酰胺酶(ESBLs)临床分离株可转移多重耐药性的分子机制。方法 采用E-试验条进行药敏检测,电转化试验筛选、分离耐药质粒,聚合酶链反应(PCR)扩增Ⅰ型整合子基因盒插入序列及其分子克隆和序列分析。结果 9个产ESBLs耐药质粒中有8个检测出了插入序列,其中7个携带了1~2种抗药性基因盒。包括氨基糖苷类钝化酶aacA4、aadA2和aadA5;甲氧苄啶钝化酶dhfrA12和dfrA17;利福平钝化酶arr-3;氯霉素外排蛋白cmlA6。基因盒功能与转化子耐药表型一致。结论 质粒定位和整合子介导的抗药性基因盒可能是导致ESBLs产酶株多重耐药性产生和(或)播散的重要原因。

关 键 词:超广谱β内酰胺酶  临床分离株  转移  多重耐药  分子机制  抗生素
修稿时间:2002年6月26日

Study on the molecular mechanism of transferable multiple-antibiotic resistance in extended-spectrum beta-lactamase -producing clinical isolates
LU Jian,TANG Ying-chun,WU Ben-quan,ZHANG Kou-xing,ZHANG Tian-tuo,BI Xiao-gang,ZHU Jia-xin,TAN Shu-qing.Study on the molecular mechanism of transferable multiple-antibiotic resistance in extended-spectrum beta-lactamase -producing clinical isolates[J].Chinese Journal of Tuberculosis and Respiratory Diseases,2003,26(4):199-202.
Authors:LU Jian  TANG Ying-chun  WU Ben-quan  ZHANG Kou-xing  ZHANG Tian-tuo  BI Xiao-gang  ZHU Jia-xin  TAN Shu-qing
Institution:Department of Respiratory Medicine, The Third Affiliated Hospital of Sun Yat-sen university, Guangzhou 510630, China.
Abstract:Objective To investigate the molecular mechanism of transferable multiple-antibiotic resistance in extended-spectrum beta-lactamases(ESBLs) producing isolates. Methods Antibiotics susceptibility was tested by E-test method, and multi-resistance plasmids were screened and isolated by extracting transformant plasmids. Inserted gene Cassettes of class 1 integron were amplified and analyzed by polymerase chain reaction(PCR) and DNA sequencing. Results Eight of the nine ESBL-producing plasmids were found to comprise class 1 integron sequence, of them 7 harbored 1 or 2 antibiotic resistant gene cassettes which encoding resistance to aminoglycosides (aacA4,aadA2 or aadA5),trimethoprim(dhfrA12 or dfrA17),rifampicin(arr-3) and chloramphenicol(cmlA6). The function of these gene cassettes corresponded to the resistance profiles of their electro-transformants. Conclusion Multi-resistance gene cassettes located on plasmids and mediated by class 1 integron may play an important role in causing the development and dissemination of multiple-antibiotic resistance in ESBL-producing clinical isolates .
Keywords:Extended-spectrum beta-lactamases  Drug resistance  multiple  Integron  Sequence analysis  DNA
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