Probe melting analysis for rapid detection of ethambutol-resistant mutations in Mycobacterium tuberculosis clinical isolates
10.3760/cma.j.issn.1009-9158.2011.02.008
- VernacularTitle:探针熔解分析法快速检测结核分枝杆菌乙胺丁醇耐药突变
- Author:
Rongrong ZHENG
;
Xiaoyun CHEN
;
Jun FU
;
Xiangdong ZHANG
;
Huixin WEN
;
Siyu HU
;
Jianjun NIU
;
Qingge LI
- Publication Type:Journal Article
- Keywords:
Mycobacterium tuberculosis;
Ethambutol;
Drug resistance,bacterial;
Mutation;
Polymerase chain reaction
- From:
Chinese Journal of Laboratory Medicine
2011;34(2):130-134
- CountryChina
- Language:Chinese
-
Abstract:
Objective To evaluate the potential use of a probe melting analysis (PMA) assay in detecting the embB mutations which confer resistance against ethambutol in Mycobacterium tuberculosis. Methods The analysis sensitivity and specificity of PMA were investigated by detecting a serially diluted H37 Rv DNA and a reference panel from National Institute for the Control of Pharmaceutical and Biological Product. Six hundred and thirteen sputum samples were collected from the Xiamen Center for Disease Control and Prevention, Xiamen First Hospital and Center for Zhangzhou Disease Control and Prevention from September 2009 to April 2010. The PMA assay was then evaluated by detecting 613 clinical isolates and the results were compared with the sequencing results. Results The PMA assay could specifically detect Mycobacterium tuberculosis and had a limit of detection of 3 copies per reaction. The assay results with 613 clinical isolates showed that PMA gave a 100% concordance with sequencing in the 583 qualified samples, among which 34 were mutations at embB 306,23 at embB 378-380, 3 at embB 406 and 3 at embB 497. Conclusions PMA assay is a sensitive and specific method enabling efficient detection of common embB mutations causing ethambutol-resistance. The rapidness of this method together with its reliability would facilitate its use in routine testing.
