Direct identification of mycobacteria from smear-positive sputum samples using an improved multiplex polymerase chain reaction assay

被引:9
|
作者
Chia, Ju-Hsin [1 ,2 ]
Wu, Tsu-Lan [1 ,2 ]
Su, Lin-Hui [1 ,2 ]
Kuo, An-Jing [1 ,2 ]
Lai, Hsin-Chih [1 ]
机构
[1] Chang Gung Univ, Dept Med Biotechnol & Lab Sci, Tao Yuan, Taiwan
[2] Chang Gung Mem Hosp, Dept Lab Med, Tao Yuan, Taiwan
关键词
Multiplex PCR assay; Mycobacterium; Direct identification; REAL-TIME PCR; TUBERCULOSIS COMPLEX MEMBERS; NONTUBERCULOUS MYCOBACTERIA; CLINICAL-SIGNIFICANCE; RAPID IDENTIFICATION; DIFFERENTIATION; EPIDEMIOLOGY; INFECTION; SPECIMENS;
D O I
10.1016/j.diagmicrobio.2011.12.008
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The rapid identification of mycobacteria from smear-positive sputum samples is very important. To identify the Mycobacterium tuberculosis complex (MTBC) and frequently isolated nontuberculous mycobacteria strains directly from smear-positive sputum samples, an improved multiplex polymerase chain reaction (PCR) assay was developed. Nine pairs of primers targeting the 16S-23S rDNA internal transcribed spacer-1, hsp65, and the early secretory antigen (ESAT-6) gene sequences were developed, and their efficacy was evaluated in comparison to traditional culturing and 16S rRNA gene sequencing methods. A total of 200 smear- and culture-positive sputum specimens collected between November 2005 and May 2006 were used for the analysis. The results of the assay showed an accurate identification rate for acid-fast bacilli (AFB) 3+, AFB 2+, and AFB rare/1+ samples of 98%, 95%, and 53%, respectively. The improved multiplex PCR method saves time and has advantages for identifying mycobacteria from AFB 2+ and 3+ sputum samples. The method is suitable for use in countries with a high MTBC prevalence rate. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:340 / 349
页数:10
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