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中国防痨杂志 ›› 2011, Vol. 33 ›› Issue (11): 713-717.

• 论著 • 上一篇    下一篇

PCR测序和基因芯片快速鉴定分枝杆菌菌种的应用研究

王峰 朱玉梅 桂静 蓝雅玲   

  1. 518020 深圳市慢性病防治中心病原检验科
  • 收稿日期:2011-03-16 出版日期:2011-11-10 发布日期:2012-01-20
  • 通信作者: 王峰 E-mail:biowangfeng@163.com
  • 基金资助:

    “十一五”国家重大科技专项(2009ZX100032018;2008ZX10003-004)

Comparison of PCR sequencing and DNA microarray for rapid identification of mycobacterium species

WANG Feng, ZHU Yu-mei, GUI Jing, LAN Ya-ling   

  1. Department of Pathogenic Laboratory, Shenzhen Center for Chronic Disease Control, Shenzhen 518020, China
  • Received:2011-03-16 Online:2011-11-10 Published:2012-01-20
  • Contact: WANG Feng E-mail:biowangfeng@163.com

摘要: 目的  评价2种分枝杆菌菌种快速鉴定方法的临床应用价值。方法  分别用16S~23S rDNA转录间隔序列(ITS)PCR-直接测序和基于16S rRNA基因的基因芯片检测21株分枝杆菌标准菌株和50株临床分离株。结果  21株分枝杆菌标准株中,ITS PCR测序法将18株准确鉴定到种,结核分枝杆菌、非洲分枝杆菌菌株只能鉴定到结核分枝杆菌复合群,海分枝杆菌无法鉴别是海分枝杆菌还是溃疡分枝杆菌;芯片法正确鉴定16株,1株胃分枝杆菌鉴定为堪萨斯分枝杆菌,3株不在芯片检测范围内。50株临床菌株中, 47株2种方法结果一致,1株不在芯片检测范围内。结论  基因芯片鉴定分枝杆菌快速、特异,准确性高,临床常规开展应用需要进一步研究。

关键词: 分枝杆菌属, 聚合酶链反应, 寡核苷酸序列分析

Abstract: Objective  To evaluate the value on rDNA sequencing of 16S-23S internal transcription space (ITS) and DNA microarray based on 16S rDNA for the rapid identification of mycobacterial species. Methods   21 mycobacterium reference strains and 50 clinical isolates were simultaneously identified by DNA sequencing and DNA microarray. Results  Of 21 mycobacterium reference strains, 18 were identified correctly at species level by DNA sequencing.  M.africanum and  M.tuberculosis strains were identified as M.tuberculosis complex, and M.marinum strain was identified as M.marinum/M.ulcerans. 16 strains were identified correctly by DNA microarray, but  1 M.gastri strain was identified as M.kansasii, 3 strains were absent of the specific probes in the microarray. Of 50 clinical isolates, 47 were consistent by DNA sequencing and DNA microarray, and one M.lentiflavum isolates was not identified by DNA microarray due to the absence of the specific probe. Conclusion  DNA microarray was a specific, accurate method for the rapid identification of most clinically relevant mycobacteria.

Key words: Mycobacterium, Polymerase chain reaction, Oligonucleotide array sequence analysis