Cargando…

Evaluation of in-house polymerase chain reaction assay sensitivity, can it be utilized in limited-resources settings?

Background: Polymerase chain reaction (PCR) assay has widely used for the detection of tuberculosis (TB). This study tried to compare in-house PCR with some well-known commercial PCR kits for detection of TB agent. Methods: Clinical samples obtained from 620 TB suspected patients were analyzed for t...

Descripción completa

Detalles Bibliográficos
Autores principales: Dorudinia, Atosa, Shamaei, Masoud, Karimi, Shirin, Javadi, Alireza, Mohammadi Ziazi, Leila, Pourabdollah, Mihan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iran University of Medical Sciences 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313456/
https://www.ncbi.nlm.nih.gov/pubmed/25679005
_version_ 1782355219907084288
author Dorudinia, Atosa
Shamaei, Masoud
Karimi, Shirin
Javadi, Alireza
Mohammadi Ziazi, Leila
Pourabdollah, Mihan
author_facet Dorudinia, Atosa
Shamaei, Masoud
Karimi, Shirin
Javadi, Alireza
Mohammadi Ziazi, Leila
Pourabdollah, Mihan
author_sort Dorudinia, Atosa
collection PubMed
description Background: Polymerase chain reaction (PCR) assay has widely used for the detection of tuberculosis (TB). This study tried to compare in-house PCR with some well-known commercial PCR kits for detection of TB agent. Methods: Clinical samples obtained from 620 TB suspected patients were analyzed for the diagnosis of Mycobacterium tuberculosis complex (MTC) by in-house PCR. All samples were obtained through pulmonary specimens consisted of 384 sputum, 148 bronchial aspirates and 88 pleural effusions. Results: Considering culture as a golden criterion, in which its diagnostic sensitivity and specificity of PCR assay were 87.7% and 85.6%, respectively. The findings of this study also indicate 22.1% (137/620) of the specimens were detected as MTC by PCR. Both PCR and culture confirmed presence of MTC in 57 of the samples. In comparison to culture, the diagnostic sensitivity of PCR for sputum was 87.5% (42/48), bronchial aspirates 100% (12/12), and 60% (3/5) for pleural effusions. The sensitivity of in-house PCR method is comparable with the sensitivity of Amplicor and Cobas TaqMan for MTC. Conclusion: The study illustrates the in-house PCR assay for detection of MTC has high sensitivity and specificity versus approved commercial kits. This could be reliable test in the diagnosis of MTC in resource-limited countries.
format Online
Article
Text
id pubmed-4313456
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Iran University of Medical Sciences
record_format MEDLINE/PubMed
spelling pubmed-43134562015-02-12 Evaluation of in-house polymerase chain reaction assay sensitivity, can it be utilized in limited-resources settings? Dorudinia, Atosa Shamaei, Masoud Karimi, Shirin Javadi, Alireza Mohammadi Ziazi, Leila Pourabdollah, Mihan Med J Islam Repub Iran Original Article Background: Polymerase chain reaction (PCR) assay has widely used for the detection of tuberculosis (TB). This study tried to compare in-house PCR with some well-known commercial PCR kits for detection of TB agent. Methods: Clinical samples obtained from 620 TB suspected patients were analyzed for the diagnosis of Mycobacterium tuberculosis complex (MTC) by in-house PCR. All samples were obtained through pulmonary specimens consisted of 384 sputum, 148 bronchial aspirates and 88 pleural effusions. Results: Considering culture as a golden criterion, in which its diagnostic sensitivity and specificity of PCR assay were 87.7% and 85.6%, respectively. The findings of this study also indicate 22.1% (137/620) of the specimens were detected as MTC by PCR. Both PCR and culture confirmed presence of MTC in 57 of the samples. In comparison to culture, the diagnostic sensitivity of PCR for sputum was 87.5% (42/48), bronchial aspirates 100% (12/12), and 60% (3/5) for pleural effusions. The sensitivity of in-house PCR method is comparable with the sensitivity of Amplicor and Cobas TaqMan for MTC. Conclusion: The study illustrates the in-house PCR assay for detection of MTC has high sensitivity and specificity versus approved commercial kits. This could be reliable test in the diagnosis of MTC in resource-limited countries. Iran University of Medical Sciences 2014-11-08 /pmc/articles/PMC4313456/ /pubmed/25679005 Text en © 2014 Iran University of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0), which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Dorudinia, Atosa
Shamaei, Masoud
Karimi, Shirin
Javadi, Alireza
Mohammadi Ziazi, Leila
Pourabdollah, Mihan
Evaluation of in-house polymerase chain reaction assay sensitivity, can it be utilized in limited-resources settings?
title Evaluation of in-house polymerase chain reaction assay sensitivity, can it be utilized in limited-resources settings?
title_full Evaluation of in-house polymerase chain reaction assay sensitivity, can it be utilized in limited-resources settings?
title_fullStr Evaluation of in-house polymerase chain reaction assay sensitivity, can it be utilized in limited-resources settings?
title_full_unstemmed Evaluation of in-house polymerase chain reaction assay sensitivity, can it be utilized in limited-resources settings?
title_short Evaluation of in-house polymerase chain reaction assay sensitivity, can it be utilized in limited-resources settings?
title_sort evaluation of in-house polymerase chain reaction assay sensitivity, can it be utilized in limited-resources settings?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313456/
https://www.ncbi.nlm.nih.gov/pubmed/25679005
work_keys_str_mv AT dorudiniaatosa evaluationofinhousepolymerasechainreactionassaysensitivitycanitbeutilizedinlimitedresourcessettings
AT shamaeimasoud evaluationofinhousepolymerasechainreactionassaysensitivitycanitbeutilizedinlimitedresourcessettings
AT karimishirin evaluationofinhousepolymerasechainreactionassaysensitivitycanitbeutilizedinlimitedresourcessettings
AT javadialireza evaluationofinhousepolymerasechainreactionassaysensitivitycanitbeutilizedinlimitedresourcessettings
AT mohammadiziazileila evaluationofinhousepolymerasechainreactionassaysensitivitycanitbeutilizedinlimitedresourcessettings
AT pourabdollahmihan evaluationofinhousepolymerasechainreactionassaysensitivitycanitbeutilizedinlimitedresourcessettings