文章摘要
刘敬华,KristinKremer,ChristinePourcel,ArnoutMulder,刘志广,赵秀芹,万康林.IS61 10限制性片段多态性分析标准方法<\b>的建立及其在结核分枝杆菌分子分型中的应用[J].中华流行病学杂志,2008,29(8):801-805
IS61 10限制性片段多态性分析标准方法<\b>的建立及其在结核分枝杆菌分子分型中的应用
stablishment and application of a standard IS61 1 0-RFLP method in the study of molecular genotyping analysis on Mycobacterium tuberculosis
投稿时间:2008-02-03  修订日期:2012-06-18
DOI:
中文关键词: 结核分枝杆菌;IS6110限制性片段多态性分析;评价
英文关键词: Mycobacterium tuberculosis;Standard IS6110-restriction fragment lengthpolymorphism method;Evaluation
基金项目:国家自然科学基金资助项目(30471526);欧盟基金资助项目(012166)
作者单位E-mail
刘敬华 中国疾病预防控制中心传染病预防控制所传染病预防控制国家重点实验室,北京102206 wankenglin@icdc.cn 
KristinKremer Mycobacteria Reference Unit, Diagnostic Laboratory of Infectious Diseases and Perinatal Screening,National Institute of Pubulic Health and the Enviroment, Bilthoven, The Netherlands  
ChristinePourcel Christine Pourel Genome, Polymorphism, and Minisatellites (GPMS), Institute of Genetics and Microbiology (IGM), France  
ArnoutMulder Mycobacteria Reference Unit, Diagnostic Laboratory of Infectious Diseases and Perinatal Screening,National Institute of Pubulic Health and the Enviroment, Bilthoven, The Netherlands  
刘志广 中国疾病预防控制中心传染病预防控制所传染病预防控制国家重点实验室,北京102206  
赵秀芹 中国疾病预防控制中心传染病预防控制所传染病预防控制国家重点实验室,北京102206  
万康林 中国疾病预防控制中心传染病预防控制所传染病预防控制国家重点实验室,北京102206  
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中文摘要:
      目的<\b> 建立IS6110限制性片段多态性分析(IS6110.RFLP)标准方法<\b>并评价该方法<\b>的分型能力。方法<\b>采用核酸提取、PCR、限制性内切酶分析、Southern杂交、琼脂糖凝胶电泳等技术,结合Gel.Pro analyzer 3.1和BioNumeries(Version 5.0)软件,对78株结核分枝杆菌插入序列IS6110.RFLP进行分析。结果<\b>确定标准化的IS6110.RFLP技术,包括核酸提取、PCR、限制性内切酶分析、Southern杂交、琼脂糖凝胶电泳等实验步骤及标化参数的相关数据分析软件的使用;采用该技术,将78株结核分枝杆菌分为75个不同的基因型,分别归属于11个基因簇,其中有52株归属于同一个基因簇,占菌株总数的66.7%(52/78)。结论<\b>建电标准化的IS6110.RFLP技术方案,该方法<\b>具有很强的基因分型和株水平鉴定能力。可用于结核病的病原学监测。
英文摘要:
      Objective To develop a standardized IS6110-restriction fragment length polymorphism (RFLP) method, used for evaluating the capacity of genotyping. Methods IS6110-RFLP of 78 Mycobacterium (M.) tuberculosis strains were studied by bio-molecular techniques including DNA isolation, PCR, restriction endonuclease enzyme analysis, southern blotting, agarose gel electrophoresis,together with data analysis by software Gel-Pro analyzer 3.1 and BioNumerics (Version 5.0). Results IS6110-RFLP method was established and standardized successfully, including DNA isolation, PCR,restriction endonuclease enzyme analysis, southern blotting, agarose gel electrophoresis and usage of the analysis software with standard parameters. By this method, 78 M. tuberculosis isolates were classified into 75 genotypes which belonged to 11 different clusters. Of all the isolates, 66.7 % (52/78) belonged to a main cluster. Conclusion Standard IS6110-RFLP method was established successfully. This method had powerful capacity for genotyping and strain level identification and could be used for the surveillance on pathogens of M. tuberculosis in China.
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