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评估BACTEC MGIT 960系统和刃天青微量滴定法用于结核分枝杆菌对二线药物药敏试验的情况。

Evaluation of the BACTEC MGIT 960 system and the resazurin microtiter assay for susceptibility testing of Mycobacterium tuberculosis to second-line drugs.

作者信息

Gallo Juliana Failde, Pinhata Juliana Maira Watanabe, Saraceni Claudia Patara, de Oliveira Rosangela Siqueira

机构信息

Núcleo de Tuberculose e Micobacterioses, Centro de Bacteriologia, Instituto Adolfo Lutz, Av. Dr. Arnaldo, 351 - 9° andar, 01246-902 São Paulo, SP, Brazil.

Núcleo de Tuberculose e Micobacterioses, Centro de Bacteriologia, Instituto Adolfo Lutz, Av. Dr. Arnaldo, 351 - 9° andar, 01246-902 São Paulo, SP, Brazil.

出版信息

J Microbiol Methods. 2017 Aug;139:168-171. doi: 10.1016/j.mimet.2017.06.007. Epub 2017 Jun 7.

Abstract

Drug resistance in tuberculosis is a major threat to public health and control of the disease worldwide. Given the need of a rapid and accurate detection of Mycobacterium tuberculosis resistance to second-line drugs, this study evaluated the performance of the BACTEC MGIT 960 for second-line, drug susceptibility testing in comparison with the resazurin microtiter assay (REMA), in order to implement the automated methodology in the diagnostic routine of a reference laboratory. Drug susceptibility testing (DST) for second-line drugs of 151 MDR M. tuberculosis clinical isolates was performed by both BACTEC MGIT 960 and REMA, and a panel of 26 M. tuberculosis reference isolates from a proficiency test was tested by the BACTEC MGIT 960. DST for second-line drugs by the BACTEC MGIT 960 system was more rapid, highly reproducible and showed 100% of proficiency. After these results, this methodology was successfully implemented in our diagnostic routine for all MDR-TB patients.

摘要

结核病耐药性是对全球公共卫生和疾病控制的重大威胁。鉴于需要快速准确地检测结核分枝杆菌对二线药物的耐药性,本研究评估了BACTEC MGIT 960在二线药物敏感性测试方面的性能,并与刃天青微量滴定法(REMA)进行比较,以便在参考实验室的诊断常规中采用自动化方法。对151株耐多药结核分枝杆菌临床分离株的二线药物进行药敏试验(DST),同时采用BACTEC MGIT 960和REMA进行检测,并通过BACTEC MGIT 960对来自能力验证的26株结核分枝杆菌参考菌株进行检测。BACTEC MGIT 960系统进行二线药物的DST更快、重复性更高,且熟练度达100%。基于这些结果,该方法已成功应用于我们对所有耐多药结核病患者的诊断常规中。

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