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

被引:10
作者
Gallo, Juliana Failde [1 ]
Watanabe Pinhata, Juliana Maira [1 ]
Chimara, Erica [1 ]
Goncalves, Maria Gisele [2 ]
Fukasawa, Lucila Okuyama [2 ]
de Oliveira, Rosangela Siqueira [1 ]
机构
[1] Adolfo Lutz Inst, Ctr Bacteriol, Nucleo TB Micobacterioses, Sao Paulo, SP, Brazil
[2] Adolfo Lutz Inst, Ctr Imunol, Lab Diagnost Mol Infeccoes Bacterianas, Sao Paulo, SP, Brazil
来源
MEMORIAS DO INSTITUTO OSWALDO CRUZ | 2016年 / 111卷 / 09期
关键词
molecular diagnostics; MPT64; protein; Mycobacterium tuberculosis; real-time polymerase chain reaction; tuberculosis; NONTUBERCULOUS MYCOBACTERIA; PRESUMPTIVE IDENTIFICATION; RESPIRATORY SPECIMENS; PCR ASSAY; COMPLEX; DNA; AMPLIFICATION; MULTIPLEX; CULTURE; SMEAR;
D O I
10.1590/0074-02760160048
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
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.
引用
收藏
页码:545 / 550
页数:6
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