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预防医学  2016, Vol. 28 Issue (7): 666-670    
  论著 本期目录 | 过刊浏览 | 高级检索 |
基于新型淬灭剂建立荧光PCR甄别幽门螺杆菌克拉霉素耐药基因突变的方法
陈志勇1,罗芸2,黄忱2,叶菊莲2,应晟1,李辉3,金大智2
1.奉化市人民医院,浙江奉化 315500;
2.浙江省疾病预防控制中心;
3.上海辉睿生物科技有限公司
Establishment of an assay for identifying mutation ofclarithromycin-resistance gene of Helicobacter pylori by real timePCR with a novel fluorescence quencher
CHEN Zhi-yong, LUO Yun,HUANG Chen, YE Ju-lian, YING Shen, LI Hui, JIN Da-zhi
Fenghua People's Hospital,Ningbo,Zhejiang,315500,China
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摘要 目的 采用新型淬灭剂结合荧光PCR检测幽门螺杆菌克拉霉素耐药基因突变的检测方法。方法 根据幽门螺杆菌23S rDNA第2142和2143两个基因多态性位点设计引物和标记新型荧光淬灭剂的探针;提取幽门螺杆菌菌体总DNA,采用实时荧光定量PCR方法对收集的55株幽门螺杆菌临床分离株进行检测,同时与TaqMan探针和直接测序方法结果进行比对,进一步评价其临床实用性。结果 本试验建立的方法能特异性地甄别23S rDNA第2142和2143位点的基因多态性,除对应位点的探针出现荧光信号外,其他探针均为阴性。该方法的变异系数小于5%,样本灵敏度可达到1 copy/反应。对收集的55株幽门螺杆菌临床分离株进行检测,检测到AA型菌株36株(65.45%)、AG型菌株15株(27.27%)和GA型菌株4株(7.27%),与TaqMan探针及直接测序结果均一致。结论 本试验所建立的方法能有效甄别幽门螺杆菌克拉霉素耐药基因突变位点A2142G和A2143G。
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陈志勇
罗芸
黄忱
叶菊莲
应晟
李辉
金大智
关键词 新型淬灭剂幽门螺杆菌荧光PCR克拉霉素耐药基因检测    
AbstractObjective To establish a real time PCR assay with a novel fluorescence quencher for identification of mutation of clarithromycin-resistance gene of Helicobacter pylori.Methods Two mutations of 23S rDNA gene in Helicobacter pylori, No. 2142 and 2143, were chosen as targets for detection, and then the primers and the probe with a novel fluorescence quencher were designed. The genome DNA of Helicobacter pylori was extracted, and then detected by real time PCR reported here. Meanwhile, the specificity, reproducibility and sensitivity of the assay were evaluated. Finally, the real time PCR described here, the real time PCR based on TaqMan, and a sequencing assay were applied to detect 55 Helicobacter pylori strains isolated from clinical specimens, respectively. The results from three assays were compared with each other in order to further evaluate the applicability of this assay in clinic. Results It indicated that the mutation points related to clarithromycin-resistance, A2142G and A2143G, were identified by real time PCR with a novel fluorescence quencher rapidly and accurately. Moreover the coefficient of variation was less than 5%. The limit of detection was 100 copies/reaction. While this assay was applied directly to detect 55 Helicobacter pylori strains, the results were in accordance with those obtained from a TaqMan real time PCR and a sequencing assay, respectively. Conclusion The real time PCR described here was a simple, reliable and accurate approach and substituted for the TaqMan real time PCR for identification of two mutation points of clarithromycin-resistance, A2142G and A2143G in Helicobacter pylori. Thus, a novel tool for diagnosis of gene mutation was provided and the results might be regarded as a substantial evidence for clinical individual therapy.
Key wordsNovel fluorescence quencher    Helicobacter pylori    Real time PCR    Clarithromycin-resistance gene    Detection
          出版日期: 2016-07-25
中图分类号:  R378.2  
基金资助:浙江省自然科学基金资助项目(LY13B020003);“艾滋病和病毒性肝炎等重大传染病防治科技重大专项”课题(2013ZX10004103)
通信作者: 金大智,E-mail:dzjin@cdc.zj.cn   
作者简介: 陈志勇,本科,副主任技师,主要从事临床免疫和分子诊断工作
引用本文:   
陈志勇, 罗芸, 黄忱, 叶菊莲, 应晟, 李辉, 金大智. 基于新型淬灭剂建立荧光PCR甄别幽门螺杆菌克拉霉素耐药基因突变的方法[J]. 预防医学, 2016, 28(7): 666-670.
CHEN Zhi-yong, LUO Yun, HUANG Chen, YE Ju-lian, YING Shen, LI Hui, JIN Da-zhi. Establishment of an assay for identifying mutation ofclarithromycin-resistance gene of Helicobacter pylori by real timePCR with a novel fluorescence quencher. Preventive Medicine, 2016, 28(7): 666-670.
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http://www.zjyfyxzz.com/CN/      或      http://www.zjyfyxzz.com/CN/Y2016/V28/I7/666
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