期刊文献+

适用于结核分枝杆菌微测序耐药基因芯片的多重PCR体系的优化与评价 被引量:4

Improvement and evaluation of the multiplex PCR system suit for micro-sequencing gene chip in detecting drug resistance of Mycobacterium tuberculosis
下载PDF
导出
摘要 目的优化结核分枝杆菌耐药相关基因多重PCR反应体系并评估其优缺点。方法利用改进的方法提取结核分枝杆菌基因组DNA,优化适合扩增rpoB,katG,mabA/inhA,pncA,embB,gyrA,rpsL,rrs和eis耐药基因片段的多重PCR体系,经测序确定所扩增出的基因片段,计算PCR操作过程所用的时间和材料成本等,分析多重PCR反应体系存在的优缺点。结果经过优化煺火温度、引物浓度以及添加NH 4^+和二甲基亚砜可以较好的扩增出5重和4重PCR产物,达到两管同时扩增9个结核分枝杆菌耐药相关基因的目的。利用该条件可以扩增出全部培养出的135株菌株DNA样本和80.56%的痰菌DNA样本,并且可以缩短PCR操作时间、降低试剂耗材成本,减少操作失误。结论优化的两管多重PCR法在同时扩增9个结核分枝杆菌耐药相关基因,具有明显的优势,具有良好的实用价值。 Objective To upgrade the multiplex PCR reaction system of related gene for drug resistance of Mycobacterium tuberculosis(M.tb),and to evaluate its advantages and disadvantages.Methods Genome DNA was extracted from M.tb clinical isolates and sputum samples by modified method.The multiplex PCR systems were improved by optimizing the PCR reaction system for amplification of 9 drug resistant fragments,rpoB,katG,mabA/inhA,pncA,embB,gyrA,rpsL,rrs and eis.After amplified fragments were confirmed by sequencing,the success rates of amplification by multiplex PCR were analyzed.The advantages and shortages of the established multiplex PCR were analyzed on the operating hours and cost.Results Those 9 drug resistant gene fragments were successfully amplified in two multiplex PCR systems by optimizing the annealing temperature,primer concentrations and supplementing NH4+ and dimethyl sulfoxide.The success rates of amplification were 100% for DNA from 135 cultured strains and 80.56% for the 36 genome DNA form the sputum.This improved multiplex PCR method could shorten the operation time,reduce the cost,and minus the operation errors.Conclusion The optimized two-tube multiplex PCR method has obvious advantages in amplifying 9 drug resistance-related genes of M.tb,which shows high practical value.
作者 孙照刚 李自慧 张洪静 孙琦 潘丽萍 张宗德 许绍发 SUN Zhao-gang;LI Zi-hui;ZHANG Hong-jing;SUN Qi;PAN Li-ping;ZHANG Zong-de;XU Shao-fa(Beijing Chest Hospital Affiliated to Capital Medical University,Beijing Tuberculosis and Thoracic Tumor Research Institute,Beijing 101149,China)
出处 《临床肺科杂志》 2020年第2期163-166,共4页 Journal of Clinical Pulmonary Medicine
基金 北京市医院管理局临床医学发展专项经费(XMLX201812) 首都卫生发展科研专项(首发2018-2Z-1042)
关键词 结核病 结核分枝杆菌 耐药 基因 多重PCR tuberculosis Mycobacterium tuberculosis drug resistance gene multiplex polymerase chain reaction(multiplex PCR)
  • 相关文献

参考文献6

二级参考文献36

  • 1崔振玲,景奉香,胡忠义,吴自荣,赵建龙.基因芯片检测结核分枝杆菌利福平和异烟肼耐药性研究[J].中华结核和呼吸杂志,2004,27(7):439-441. 被引量:31
  • 2陈曦,马玙,金奇,姜广路,李传友,王庆.耐异烟肼结核分枝杆菌临床分离株耐药相关基因突变研究[J].中华结核和呼吸杂志,2005,28(4):250-253. 被引量:44
  • 3WHO Report 2009:Global tuberculosis control:epidemiology,strategy,finacing.World Health Organization,2009. 被引量:1
  • 4Shimizu Y,Dobashi K,Yoshikawa Y,et al.Five-antituberculosis drug-resistance genes detection using array system.J Clin Biochem Nutr,2008,42:228-234. 被引量:1
  • 5Garrigo M,Aragon LM,Alcaide F,et al.Multicenter laboratory evaluation of the MB/Bact mycobacterium detection system and the BACTEC MGIT 960 system in comparison with the BACTEC 460TB system for susceptibility testing of mycobacterium tuberculosis.J Clin Microbiol,2007,45:1766-1770. 被引量:1
  • 6Scarparo C,Ricordi P,Ruggiero G,et al.Evaluation of the fully automated BACTEC MGIT 960 system for testing susceptibility of mycobacterium tuberculosis to pyrazinamide,streptomycin,isoniazid,tifampin,and ethambutol and comparison with the radiometric BACTEC 460TB method.J Clin Microbiol,2004,42:1109-1114. 被引量:1
  • 7Guo, Y, Zhou Y, Wang C, et al. Rapid, accurate determination of Multidrug resistance in M. tuberculosis isolates and sputum using a biochip system. Int J Tuberc Lung Dis, 2009, 13:914- 920. 被引量:1
  • 8Mukherjee J, Rich M, Socci A, et al. Programmes and principles in treatment of multidrug-resistant tuberculosis. Lancet, 2004, 363:474-481. 被引量:1
  • 9Head SR, Parikh K, Rogers YH, et al. Solid-phase sequence scanning for drug resistance detection in tuberculosis. Mol Cell Probes, 1999, 13: 81-87. 被引量:1
  • 10Gingeras TR, Ghandour G, Wang E, et al. Simultaneous genotyping and species identification using hybridization pattern recognition analysis of generic Mycobacterium DNA arrays. Genome Res, 1998, 8: 435-448. 被引量:1

共引文献66

同被引文献43

引证文献4

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部