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Evaluation of GenoType MTBDRplus for the detection of drug-resistant Mycobacterium tuberculosis on isolates from Karachi, Pakistan

OBJECTIVE: To compare the diagnostic performance of the GenoType MRBDRplus assay with the gold standard phenotypic drug susceptibility testing in the detection of drug resistance among culture isolates obtained from patients in Karachi, Pakistan. DESIGN: Mycobacterium tuberculosis isolates were obta...

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Autores principales: Siddiqui, Sara, Brooks, Meredith B., Malik, Amyn A., Fuad, Junaid, Nazish, Ahsana, Bano, Safia, Becerra, Mercedes C., Hussain, Hamidah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6699735/
https://www.ncbi.nlm.nih.gov/pubmed/31425565
http://dx.doi.org/10.1371/journal.pone.0221485
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author Siddiqui, Sara
Brooks, Meredith B.
Malik, Amyn A.
Fuad, Junaid
Nazish, Ahsana
Bano, Safia
Becerra, Mercedes C.
Hussain, Hamidah
author_facet Siddiqui, Sara
Brooks, Meredith B.
Malik, Amyn A.
Fuad, Junaid
Nazish, Ahsana
Bano, Safia
Becerra, Mercedes C.
Hussain, Hamidah
author_sort Siddiqui, Sara
collection PubMed
description OBJECTIVE: To compare the diagnostic performance of the GenoType MRBDRplus assay with the gold standard phenotypic drug susceptibility testing in the detection of drug resistance among culture isolates obtained from patients in Karachi, Pakistan. DESIGN: Mycobacterium tuberculosis isolates were obtained from 96 consecutive tuberculosis patients found to have resistance to isoniazid from two health centers in Karachi (January-November 2017). Isolates were tested for drug resistance against rifampin and isoniazid using the MTBDRplus assay. Results were compared with conventional drug-susceptibility testing and the frequency of specific mutations were reported. RESULTS: The MTBDRplus assay had a sensitivity for rifampin resistance of 98.8% (95% CI: 93.4–100) and for isoniazid resistance of 90.6% (95% CI: 83.0–95.6). The MTBDRplus assay showed mutations in rpoB in 81 of the 96 (84.4%) isolates. Of the 87 isolates showing resistance to isoniazid via the MTBDRplus assay, 71 (74.0%) isolates had mutations in the katG gene only, 15 (15.6%) isolates had mutations in the inhA promoter region, and 1 (1.0%) showed mutations in both genes. CONCLUSION: The GenoType MTBDRplus assay in Pakistan can identify subgroups at high-risk of having isolates with mutations in the katG and/or inhA genes. Understanding the local burden of these mutations have implications for local diagnostic and treatment guidelines.
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spelling pubmed-66997352019-09-04 Evaluation of GenoType MTBDRplus for the detection of drug-resistant Mycobacterium tuberculosis on isolates from Karachi, Pakistan Siddiqui, Sara Brooks, Meredith B. Malik, Amyn A. Fuad, Junaid Nazish, Ahsana Bano, Safia Becerra, Mercedes C. Hussain, Hamidah PLoS One Research Article OBJECTIVE: To compare the diagnostic performance of the GenoType MRBDRplus assay with the gold standard phenotypic drug susceptibility testing in the detection of drug resistance among culture isolates obtained from patients in Karachi, Pakistan. DESIGN: Mycobacterium tuberculosis isolates were obtained from 96 consecutive tuberculosis patients found to have resistance to isoniazid from two health centers in Karachi (January-November 2017). Isolates were tested for drug resistance against rifampin and isoniazid using the MTBDRplus assay. Results were compared with conventional drug-susceptibility testing and the frequency of specific mutations were reported. RESULTS: The MTBDRplus assay had a sensitivity for rifampin resistance of 98.8% (95% CI: 93.4–100) and for isoniazid resistance of 90.6% (95% CI: 83.0–95.6). The MTBDRplus assay showed mutations in rpoB in 81 of the 96 (84.4%) isolates. Of the 87 isolates showing resistance to isoniazid via the MTBDRplus assay, 71 (74.0%) isolates had mutations in the katG gene only, 15 (15.6%) isolates had mutations in the inhA promoter region, and 1 (1.0%) showed mutations in both genes. CONCLUSION: The GenoType MTBDRplus assay in Pakistan can identify subgroups at high-risk of having isolates with mutations in the katG and/or inhA genes. Understanding the local burden of these mutations have implications for local diagnostic and treatment guidelines. Public Library of Science 2019-08-19 /pmc/articles/PMC6699735/ /pubmed/31425565 http://dx.doi.org/10.1371/journal.pone.0221485 Text en © 2019 Siddiqui et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Siddiqui, Sara
Brooks, Meredith B.
Malik, Amyn A.
Fuad, Junaid
Nazish, Ahsana
Bano, Safia
Becerra, Mercedes C.
Hussain, Hamidah
Evaluation of GenoType MTBDRplus for the detection of drug-resistant Mycobacterium tuberculosis on isolates from Karachi, Pakistan
title Evaluation of GenoType MTBDRplus for the detection of drug-resistant Mycobacterium tuberculosis on isolates from Karachi, Pakistan
title_full Evaluation of GenoType MTBDRplus for the detection of drug-resistant Mycobacterium tuberculosis on isolates from Karachi, Pakistan
title_fullStr Evaluation of GenoType MTBDRplus for the detection of drug-resistant Mycobacterium tuberculosis on isolates from Karachi, Pakistan
title_full_unstemmed Evaluation of GenoType MTBDRplus for the detection of drug-resistant Mycobacterium tuberculosis on isolates from Karachi, Pakistan
title_short Evaluation of GenoType MTBDRplus for the detection of drug-resistant Mycobacterium tuberculosis on isolates from Karachi, Pakistan
title_sort evaluation of genotype mtbdrplus for the detection of drug-resistant mycobacterium tuberculosis on isolates from karachi, pakistan
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6699735/
https://www.ncbi.nlm.nih.gov/pubmed/31425565
http://dx.doi.org/10.1371/journal.pone.0221485
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