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Improved diagnosis of central nervous system tuberculosis by MPB64-Target PCR

Central nervous system (CNS) tuberculosis is a serious clinical problem, the treatment of which is sometimes hampered by delayed diagnosis. Clearly, prompt laboratory diagnosis is of vital importance as the spectrum of disease is wide and abnormalities of the cerebrospinal fluid (CSF) are incredibly...

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Autores principales: Dil-Afroze, Mir, Abdul Waheed, Kirmani1, Altaf, Shakeel-ul-Rehman, Eachkoti, Rafiqa, Siddiqi, Mushtaq A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Microbiologia 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768381/
https://www.ncbi.nlm.nih.gov/pubmed/24031203
http://dx.doi.org/10.1590/S1517-83822008000200002
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author Dil-Afroze,
Mir, Abdul Waheed
Kirmani1, Altaf
Shakeel-ul-Rehman,
Eachkoti, Rafiqa
Siddiqi, Mushtaq A.
author_facet Dil-Afroze,
Mir, Abdul Waheed
Kirmani1, Altaf
Shakeel-ul-Rehman,
Eachkoti, Rafiqa
Siddiqi, Mushtaq A.
author_sort Dil-Afroze,
collection PubMed
description Central nervous system (CNS) tuberculosis is a serious clinical problem, the treatment of which is sometimes hampered by delayed diagnosis. Clearly, prompt laboratory diagnosis is of vital importance as the spectrum of disease is wide and abnormalities of the cerebrospinal fluid (CSF) are incredibly variable. Since delayed hypersensitivity is the underlying immune response, bacterial load is very low. The conventional bacteriological methods rarely detect Mycobacterium tuberculosis in CSF and are of limited use in diagnosis of tuberculous meningitis (TBM). This double blind study was, therefore, directed to the molecular analysis of CNS tuberculosis by an in-house-developed PCR targeted for amplification of a 240bp nucleotide sequence coding for MPB64 protein specific for Mycobacterium tuberculosis. Based on the clinical criteria, 47 patients with CNS tuberculosis and a control group of 10 patients having non-tubercular lesions of the CNS were included in the study. Analyses were done in three groups; one group consisting of 27 patients of TBM, a second group of 20 patients with intracranial tuberculomas and a third group of 10 patients having nontubercular lesions of the CNS acted as control. There were no false positive results by PCR and the specificity worked out to be 100%. In the three study groups, routine CSF analysis (cells and chemistry), CSF for AFB smear and culture were negative in all cases. PCR was positive for 21/27 patients (77.7% sensitivity) of the first group of TBM patients, 6/20 patients (30% sensitivity) of the second group with intracranial tuberculomas were positive by PCR and none was PCR-positive (100% specificity) in the third group. Thus, PCR was found to be more sensitive than any other conventional method in the diagnosis of clinically suspected tubercular meningitis.
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spelling pubmed-37683812013-09-12 Improved diagnosis of central nervous system tuberculosis by MPB64-Target PCR Dil-Afroze, Mir, Abdul Waheed Kirmani1, Altaf Shakeel-ul-Rehman, Eachkoti, Rafiqa Siddiqi, Mushtaq A. Braz J Microbiol Medical Microbiology Central nervous system (CNS) tuberculosis is a serious clinical problem, the treatment of which is sometimes hampered by delayed diagnosis. Clearly, prompt laboratory diagnosis is of vital importance as the spectrum of disease is wide and abnormalities of the cerebrospinal fluid (CSF) are incredibly variable. Since delayed hypersensitivity is the underlying immune response, bacterial load is very low. The conventional bacteriological methods rarely detect Mycobacterium tuberculosis in CSF and are of limited use in diagnosis of tuberculous meningitis (TBM). This double blind study was, therefore, directed to the molecular analysis of CNS tuberculosis by an in-house-developed PCR targeted for amplification of a 240bp nucleotide sequence coding for MPB64 protein specific for Mycobacterium tuberculosis. Based on the clinical criteria, 47 patients with CNS tuberculosis and a control group of 10 patients having non-tubercular lesions of the CNS were included in the study. Analyses were done in three groups; one group consisting of 27 patients of TBM, a second group of 20 patients with intracranial tuberculomas and a third group of 10 patients having nontubercular lesions of the CNS acted as control. There were no false positive results by PCR and the specificity worked out to be 100%. In the three study groups, routine CSF analysis (cells and chemistry), CSF for AFB smear and culture were negative in all cases. PCR was positive for 21/27 patients (77.7% sensitivity) of the first group of TBM patients, 6/20 patients (30% sensitivity) of the second group with intracranial tuberculomas were positive by PCR and none was PCR-positive (100% specificity) in the third group. Thus, PCR was found to be more sensitive than any other conventional method in the diagnosis of clinically suspected tubercular meningitis. Sociedade Brasileira de Microbiologia 2008 2008-06-01 /pmc/articles/PMC3768381/ /pubmed/24031203 http://dx.doi.org/10.1590/S1517-83822008000200002 Text en © Sociedade Brasileira de Microbiologia http://creativecommons.org/licenses/by-nc/3.0/ All the content of the journal, except where otherwise noted, is licensed under a Creative Commons License
spellingShingle Medical Microbiology
Dil-Afroze,
Mir, Abdul Waheed
Kirmani1, Altaf
Shakeel-ul-Rehman,
Eachkoti, Rafiqa
Siddiqi, Mushtaq A.
Improved diagnosis of central nervous system tuberculosis by MPB64-Target PCR
title Improved diagnosis of central nervous system tuberculosis by MPB64-Target PCR
title_full Improved diagnosis of central nervous system tuberculosis by MPB64-Target PCR
title_fullStr Improved diagnosis of central nervous system tuberculosis by MPB64-Target PCR
title_full_unstemmed Improved diagnosis of central nervous system tuberculosis by MPB64-Target PCR
title_short Improved diagnosis of central nervous system tuberculosis by MPB64-Target PCR
title_sort improved diagnosis of central nervous system tuberculosis by mpb64-target pcr
topic Medical Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768381/
https://www.ncbi.nlm.nih.gov/pubmed/24031203
http://dx.doi.org/10.1590/S1517-83822008000200002
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