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在高负担地区实验室常规诊断中,使用内部实时聚合酶链反应鉴定结核分枝杆菌分离株的性能。

Performance of an in-house real-time polymerase chain reaction for identification of Mycobacterium tuberculosis isolates in laboratory routine diagnosis from a high burden setting.

作者信息

Gallo Juliana Failde, Pinhata Juliana Maira Watanabe, Chimara Erica, Gonçalves Maria Gisele, Fukasawa Lucila Okuyama, Oliveira Rosangela Siqueira de

机构信息

Instituto Adolfo Lutz, Centro de Bacteriologia, Núcleo de Tuberculose e Micobacterioses, São Paulo, SP, Brasil.

Instituto Adolfo Lutz, Centro de Imunologia, Laboratório de Diagnóstico Molecular de Infecções Bacterianas, São Paulo, SP, Brasil.

出版信息

Mem Inst Oswaldo Cruz. 2016 Sep;111(9):545-50. doi: 10.1590/0074-02760160048. Epub 2016 Sep 1.

DOI:10.1590/0074-02760160048
PMID:27598243
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5027861/
Abstract

Brazil is one of the high burden countries for tuberculosis, and a rapid diagnosis is essential for effective control of the disease. In the present study, an in-house real-time polymerase chain reaction (PCR) assay targeting the mpt64 gene for identification of Mycobacterium tuberculosis complex isolates was evaluated under routine diagnosis conditions in a reference laboratory. From May 2011 to July 2012, 1,520 isolates of mycobacteria were prospectively submitted for phenotypic and/or PRA-hsp65 identification and to real-time PCR. The mpt64 real-time PCR showed 99.7% sensitivity and 96% specificity and detected 79.4% of the cases missed by phenotypic and PRA-hsp65 identification. The in-house real-time PCR assay showed high sensitivity and specificity and was successfully implemented in the routine diagnosis of tuberculosis in a reference laboratory from a high burden setting.

摘要

巴西是结核病高负担国家之一,快速诊断对于有效控制该疾病至关重要。在本研究中,在一家参考实验室的常规诊断条件下,对一种针对mpt64基因以鉴定结核分枝杆菌复合群分离株的内部实时聚合酶链反应(PCR)检测方法进行了评估。2011年5月至2012年7月,前瞻性地提交了1520株分枝杆菌分离株进行表型和/或PRA-hsp65鉴定以及实时PCR检测。mpt64实时PCR显示出99.7%的敏感性和96%的特异性,检测出了79.4%通过表型和PRA-hsp65鉴定漏检的病例。该内部实时PCR检测方法显示出高敏感性和特异性,并成功应用于来自高负担地区的一家参考实验室的结核病常规诊断。

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本文引用的文献

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Rapid detection of Mycobacterium tuberculosis complex by real-time PCR in sputum samples and its use in the routine diagnosis in a reference laboratory.通过实时聚合酶链反应在痰液样本中快速检测结核分枝杆菌复合群及其在参考实验室常规诊断中的应用
J Med Microbiol. 2015 Sep;64(9):1040-1045. doi: 10.1099/jmm.0.000121. Epub 2015 Jul 9.
2
Simultaneous detection of Mycobacterium tuberculosis complex and nontuberculous mycobacteria in respiratory specimens.同时检测呼吸道标本中的结核分枝杆菌复合体和非结核分枝杆菌。
Tuberculosis (Edinb). 2013 Nov;93(6):642-6. doi: 10.1016/j.tube.2013.07.007. Epub 2013 Aug 7.
3
Comparative study of diagnostic accuracy of established PCR assays and in-house developed sdaA PCR method for detection of Mycobacterium tuberculosis in symptomatic patients with pulmonary tuberculosis.建立的 PCR 检测方法与自行开发的 sdaA PCR 方法对肺结核症状患者中结核分枝杆菌的诊断准确性的比较研究。
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Fast test for assessing the susceptibility of Mycobacterium tuberculosis to isoniazid and rifampin by real-time PCR.实时 PCR 快速检测结核分枝杆菌对异烟肼和利福平的敏感性。
Mem Inst Oswaldo Cruz. 2012 Nov;107(7):903-8. doi: 10.1590/s0074-02762012000700011.
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