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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.
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页码:340 / 349
页数:10
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