Detection and identification of mycobacteria in sputum from suspected tuberculosis patients

<p>Abstract</p> <p>Background</p> <p>Detection of Tuberculosis agent like nontuberculous mycobacteria (NTM) species by culture and microscopic methods remains difficult and time consuming. A fast and reliable diagnosis of tuberculosis would greatly improve the control o...

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Main Authors: Yadi, Masjudi, Tandirogang Nataniel, Sultan Andi, Hatta Mochammad
Format: Article
Language:English
Published: BMC 2010-03-01
Series:BMC Research Notes
Online Access:http://www.biomedcentral.com/1756-0500/3/72
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spelling doaj-b46306375af44ea1b09c19236511e9d42020-11-25T02:29:30ZengBMCBMC Research Notes1756-05002010-03-01317210.1186/1756-0500-3-72Detection and identification of mycobacteria in sputum from suspected tuberculosis patientsYadiMasjudiTandirogang NatanielSultan AndiHatta Mochammad<p>Abstract</p> <p>Background</p> <p>Detection of Tuberculosis agent like nontuberculous mycobacteria (NTM) species by culture and microscopic methods remains difficult and time consuming. A fast and reliable diagnosis of tuberculosis would greatly improve the control of the disease. The purpose of this study is to compare the conventional multiplex PCR and multiplex PCR reverse cross blot hybridization assay to culture method in terms of mycobacteria species detection.</p> <p>Findings</p> <p>Among the 117 positively cultured samples, nontuberculous mycobacteria (NTM) species were found in 9 samples of multiplex PCR reverse cross blot hybridization assay; compared to only 3 NTM species found in our conventional multiplex PCR, and 13 NTM species were successfully identified among 162 negatively cultured samples compared to only 5 NTM species identification in conventional multiplex PCR results.</p> <p>Conclusions</p> <p>The sensitivity of the multiplex PCR reverse cross blot hybridization assay comparing to culture method was 86.03%, the specificity is 35.46%, the positive predictive value was 41.94% and the negative predictive value was 82.41%. For conventional multiplex PCR these values are 81.62%, 38.65%, 41.89%, 79.51%, respectively. Furthermore, in terms of mycobacteria species detection, the conventional multiplex PCR was relatively equal compared to the multiplex PCR reverse cross blot hybridization assay, and to be particularly having no significant discrepant results on the identification of <it>Mycobacteria tuberculosis </it>in both methods.</p> http://www.biomedcentral.com/1756-0500/3/72
collection DOAJ
language English
format Article
sources DOAJ
author Yadi
Masjudi
Tandirogang Nataniel
Sultan Andi
Hatta Mochammad
spellingShingle Yadi
Masjudi
Tandirogang Nataniel
Sultan Andi
Hatta Mochammad
Detection and identification of mycobacteria in sputum from suspected tuberculosis patients
BMC Research Notes
author_facet Yadi
Masjudi
Tandirogang Nataniel
Sultan Andi
Hatta Mochammad
author_sort Yadi
title Detection and identification of mycobacteria in sputum from suspected tuberculosis patients
title_short Detection and identification of mycobacteria in sputum from suspected tuberculosis patients
title_full Detection and identification of mycobacteria in sputum from suspected tuberculosis patients
title_fullStr Detection and identification of mycobacteria in sputum from suspected tuberculosis patients
title_full_unstemmed Detection and identification of mycobacteria in sputum from suspected tuberculosis patients
title_sort detection and identification of mycobacteria in sputum from suspected tuberculosis patients
publisher BMC
series BMC Research Notes
issn 1756-0500
publishDate 2010-03-01
description <p>Abstract</p> <p>Background</p> <p>Detection of Tuberculosis agent like nontuberculous mycobacteria (NTM) species by culture and microscopic methods remains difficult and time consuming. A fast and reliable diagnosis of tuberculosis would greatly improve the control of the disease. The purpose of this study is to compare the conventional multiplex PCR and multiplex PCR reverse cross blot hybridization assay to culture method in terms of mycobacteria species detection.</p> <p>Findings</p> <p>Among the 117 positively cultured samples, nontuberculous mycobacteria (NTM) species were found in 9 samples of multiplex PCR reverse cross blot hybridization assay; compared to only 3 NTM species found in our conventional multiplex PCR, and 13 NTM species were successfully identified among 162 negatively cultured samples compared to only 5 NTM species identification in conventional multiplex PCR results.</p> <p>Conclusions</p> <p>The sensitivity of the multiplex PCR reverse cross blot hybridization assay comparing to culture method was 86.03%, the specificity is 35.46%, the positive predictive value was 41.94% and the negative predictive value was 82.41%. For conventional multiplex PCR these values are 81.62%, 38.65%, 41.89%, 79.51%, respectively. Furthermore, in terms of mycobacteria species detection, the conventional multiplex PCR was relatively equal compared to the multiplex PCR reverse cross blot hybridization assay, and to be particularly having no significant discrepant results on the identification of <it>Mycobacteria tuberculosis </it>in both methods.</p>
url http://www.biomedcentral.com/1756-0500/3/72
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AT masjudi detectionandidentificationofmycobacteriainsputumfromsuspectedtuberculosispatients
AT tandirogangnataniel detectionandidentificationofmycobacteriainsputumfromsuspectedtuberculosispatients
AT sultanandi detectionandidentificationofmycobacteriainsputumfromsuspectedtuberculosispatients
AT hattamochammad detectionandidentificationofmycobacteriainsputumfromsuspectedtuberculosispatients
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