Utility of multiplex real-time PCR in the diagnosis of extrapulmonary tuberculosis
Objective: The diagnosis of extrapulmonary tuberculosis is still a challenge because of its pauci-bacillary nature. The aim of the study was to evaluate the role of a multiplex PCR assay in the diagnosis of extrapulmonary tuberculosis and to compare the efficiency of two targets, IS6110 and MPB64 to...
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doaj-d65e3dc510be40f28d8257c50df7b5952020-11-25T03:16:22ZengElsevierBrazilian Journal of Infectious Diseases1413-86702016-05-01203235241S1413-86702016000300003Utility of multiplex real-time PCR in the diagnosis of extrapulmonary tuberculosisReena Raveendran0Chand Wattal1Department of Clinical Microbiology & Immunology, Sir Ganga Ram Hospital, New Delhi, IndiaCorresponding author.; Department of Clinical Microbiology & Immunology, Sir Ganga Ram Hospital, New Delhi, IndiaObjective: The diagnosis of extrapulmonary tuberculosis is still a challenge because of its pauci-bacillary nature. The aim of the study was to evaluate the role of a multiplex PCR assay in the diagnosis of extrapulmonary tuberculosis and to compare the efficiency of two targets, IS6110 and MPB64 to detect Mycobacterium tuberculosis. Methods: 150 extrapulmonary samples (61 pus/aspirate, 46 tissue, 32 body fluids, and 11 urine) from clinically suspected cases of tuberculosis were included in the study. All the samples were subjected to direct fluorescent microscopy, TB culture (BacT/ALERT 3D, biomerieux, Durham, North Carolina, USA) and a Multiplexed Tandem PCR targeting two mycobacterial DNA sequences, IS6110 and MPB64. Master-Mix reagents and primers were prepared by AusDiagnostics Pvt. Ltd (Alexandria, New South Wales, Australia). The performance of the assay was assessed using a composite gold standard, which included clinical characteristics, microbiology smear as well as culture, histopathology, cytology, radiology, and response to antitubercular therapy. Results: 20.3%, 23.6%, and 45.3% of specimens were positive by smear, culture, and PCR, respectively. The sensitivity and specificity of the multiplex PCR was 91.9% and 88.4%, respectively, using the composite gold standard. Positive and negative predictive values of the PCR were estimated as 85.1% and 93.8%, respectively. Higher positivity was observed with target IS6110 (44.6%) as compared to target MPB64 (18.9%). The sensitivities of IS6110 and MPB64 individual targets were 90.3% and 64.5%, respectively, and specificities were 88.4% and 97.7%, respectively. Conclusion: PCR can play an important role in rapid and accurate diagnosis of extrapulmonary tuberculosis. IS6110 alone is an effective target in our part of the country. Keywords: Extrapulmonary tuberculosis, Multiplex PCR, IS6110, MPB64http://www.sciencedirect.com/science/article/pii/S1413867016300393 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Reena Raveendran Chand Wattal |
spellingShingle |
Reena Raveendran Chand Wattal Utility of multiplex real-time PCR in the diagnosis of extrapulmonary tuberculosis Brazilian Journal of Infectious Diseases |
author_facet |
Reena Raveendran Chand Wattal |
author_sort |
Reena Raveendran |
title |
Utility of multiplex real-time PCR in the diagnosis of extrapulmonary tuberculosis |
title_short |
Utility of multiplex real-time PCR in the diagnosis of extrapulmonary tuberculosis |
title_full |
Utility of multiplex real-time PCR in the diagnosis of extrapulmonary tuberculosis |
title_fullStr |
Utility of multiplex real-time PCR in the diagnosis of extrapulmonary tuberculosis |
title_full_unstemmed |
Utility of multiplex real-time PCR in the diagnosis of extrapulmonary tuberculosis |
title_sort |
utility of multiplex real-time pcr in the diagnosis of extrapulmonary tuberculosis |
publisher |
Elsevier |
series |
Brazilian Journal of Infectious Diseases |
issn |
1413-8670 |
publishDate |
2016-05-01 |
description |
Objective: The diagnosis of extrapulmonary tuberculosis is still a challenge because of its pauci-bacillary nature. The aim of the study was to evaluate the role of a multiplex PCR assay in the diagnosis of extrapulmonary tuberculosis and to compare the efficiency of two targets, IS6110 and MPB64 to detect Mycobacterium tuberculosis. Methods: 150 extrapulmonary samples (61 pus/aspirate, 46 tissue, 32 body fluids, and 11 urine) from clinically suspected cases of tuberculosis were included in the study. All the samples were subjected to direct fluorescent microscopy, TB culture (BacT/ALERT 3D, biomerieux, Durham, North Carolina, USA) and a Multiplexed Tandem PCR targeting two mycobacterial DNA sequences, IS6110 and MPB64. Master-Mix reagents and primers were prepared by AusDiagnostics Pvt. Ltd (Alexandria, New South Wales, Australia). The performance of the assay was assessed using a composite gold standard, which included clinical characteristics, microbiology smear as well as culture, histopathology, cytology, radiology, and response to antitubercular therapy. Results: 20.3%, 23.6%, and 45.3% of specimens were positive by smear, culture, and PCR, respectively. The sensitivity and specificity of the multiplex PCR was 91.9% and 88.4%, respectively, using the composite gold standard. Positive and negative predictive values of the PCR were estimated as 85.1% and 93.8%, respectively. Higher positivity was observed with target IS6110 (44.6%) as compared to target MPB64 (18.9%). The sensitivities of IS6110 and MPB64 individual targets were 90.3% and 64.5%, respectively, and specificities were 88.4% and 97.7%, respectively. Conclusion: PCR can play an important role in rapid and accurate diagnosis of extrapulmonary tuberculosis. IS6110 alone is an effective target in our part of the country. Keywords: Extrapulmonary tuberculosis, Multiplex PCR, IS6110, MPB64 |
url |
http://www.sciencedirect.com/science/article/pii/S1413867016300393 |
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