Rapid detection and differentiation of mycobacterial species using a multiplex PCR system

Introduction The early diagnosis of mycobacterial infections is a critical step for initiating treatment and curing the patient. Molecular analytical methods have led to considerable improvements in the speed and accuracy of mycobacteria detection. Methods The purpose of this study was to evaluate...

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Main Authors: Andrea Santos Lima, Rafael Silva Duarte, Lilian Maria Lapa Montenegro, Haiana Charifker Schindler
Format: Article
Language:English
Published: Sociedade Brasileira de Medicina Tropical (SBMT) 2013-07-01
Series:Revista da Sociedade Brasileira de Medicina Tropical
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0037-86822013000400447&lng=en&tlng=en
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author Andrea Santos Lima
Rafael Silva Duarte
Lilian Maria Lapa Montenegro
Haiana Charifker Schindler
author_facet Andrea Santos Lima
Rafael Silva Duarte
Lilian Maria Lapa Montenegro
Haiana Charifker Schindler
author_sort Andrea Santos Lima
collection DOAJ
description Introduction The early diagnosis of mycobacterial infections is a critical step for initiating treatment and curing the patient. Molecular analytical methods have led to considerable improvements in the speed and accuracy of mycobacteria detection. Methods The purpose of this study was to evaluate a multiplex polymerase chain reaction system using mycobacterial strains as an auxiliary tool in the differential diagnosis of tuberculosis and diseases caused by nontuberculous mycobacteria (NTM) Results Forty mycobacterial strains isolated from pulmonary and extrapulmonary origin specimens from 37 patients diagnosed with tuberculosis were processed. Using phenotypic and biochemical characteristics of the 40 mycobacteria isolated in LJ medium, 57.5% (n=23) were characterized as the Mycobacterium tuberculosis complex (MTBC) and 20% (n=8) as nontuberculous mycobacteria (NTM), with 22.5% (n=9) of the results being inconclusive. When the results of the phenotypic and biochemical tests in 30 strains of mycobacteria were compared with the results of the multiplex PCR, there was 100% concordance in the identification of the MTBC and NTM species, respectively. A total of 32.5% (n=13) of the samples in multiplex PCR exhibited a molecular pattern consistent with NTM, thus disagreeing with the final diagnosis from the attending physician. Conclusions Multiplex PCR can be used as a differential method for determining TB infections caused by NTM a valuable tool in reducing the time necessary to make clinical diagnoses and begin treatment. It is also useful for identifying species that were previously not identifiable using conventional biochemical and phenotypic techniques.
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spelling doaj.art-32d91a0a807e403f9d6c0c748aa68b2c2022-12-22T00:22:32ZengSociedade Brasileira de Medicina Tropical (SBMT)Revista da Sociedade Brasileira de Medicina Tropical1678-98492013-07-0146444745210.1590/0037-8682-0097-2013S0037-86822013000400447Rapid detection and differentiation of mycobacterial species using a multiplex PCR systemAndrea Santos LimaRafael Silva DuarteLilian Maria Lapa MontenegroHaiana Charifker SchindlerIntroduction The early diagnosis of mycobacterial infections is a critical step for initiating treatment and curing the patient. Molecular analytical methods have led to considerable improvements in the speed and accuracy of mycobacteria detection. Methods The purpose of this study was to evaluate a multiplex polymerase chain reaction system using mycobacterial strains as an auxiliary tool in the differential diagnosis of tuberculosis and diseases caused by nontuberculous mycobacteria (NTM) Results Forty mycobacterial strains isolated from pulmonary and extrapulmonary origin specimens from 37 patients diagnosed with tuberculosis were processed. Using phenotypic and biochemical characteristics of the 40 mycobacteria isolated in LJ medium, 57.5% (n=23) were characterized as the Mycobacterium tuberculosis complex (MTBC) and 20% (n=8) as nontuberculous mycobacteria (NTM), with 22.5% (n=9) of the results being inconclusive. When the results of the phenotypic and biochemical tests in 30 strains of mycobacteria were compared with the results of the multiplex PCR, there was 100% concordance in the identification of the MTBC and NTM species, respectively. A total of 32.5% (n=13) of the samples in multiplex PCR exhibited a molecular pattern consistent with NTM, thus disagreeing with the final diagnosis from the attending physician. Conclusions Multiplex PCR can be used as a differential method for determining TB infections caused by NTM a valuable tool in reducing the time necessary to make clinical diagnoses and begin treatment. It is also useful for identifying species that were previously not identifiable using conventional biochemical and phenotypic techniques.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0037-86822013000400447&lng=en&tlng=enMycobacterium tuberculosis complexNontuberculous mycobacteriaDiagnosisPolymerase chain reactionMultiplex
spellingShingle Andrea Santos Lima
Rafael Silva Duarte
Lilian Maria Lapa Montenegro
Haiana Charifker Schindler
Rapid detection and differentiation of mycobacterial species using a multiplex PCR system
Revista da Sociedade Brasileira de Medicina Tropical
Mycobacterium tuberculosis complex
Nontuberculous mycobacteria
Diagnosis
Polymerase chain reaction
Multiplex
title Rapid detection and differentiation of mycobacterial species using a multiplex PCR system
title_full Rapid detection and differentiation of mycobacterial species using a multiplex PCR system
title_fullStr Rapid detection and differentiation of mycobacterial species using a multiplex PCR system
title_full_unstemmed Rapid detection and differentiation of mycobacterial species using a multiplex PCR system
title_short Rapid detection and differentiation of mycobacterial species using a multiplex PCR system
title_sort rapid detection and differentiation of mycobacterial species using a multiplex pcr system
topic Mycobacterium tuberculosis complex
Nontuberculous mycobacteria
Diagnosis
Polymerase chain reaction
Multiplex
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0037-86822013000400447&lng=en&tlng=en
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