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Early detection of MDR Mycobacterium tuberculosis mutations in Pakistan

The result of improper treatment has led to the rise of Multidrug-resistant (MDR) strains. This concern still exists in Pakistan. In order to save energy, time and resources an early detection of resistant cases is imperative. Thus, a treated group of 100 isolates and a control group of 56 untreated...

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Autores principales: Aftab, Ayma, Afzal, Samia, Qamar, Zahida, Idrees, Muhammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373971/
https://www.ncbi.nlm.nih.gov/pubmed/34408186
http://dx.doi.org/10.1038/s41598-021-96116-x
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author Aftab, Ayma
Afzal, Samia
Qamar, Zahida
Idrees, Muhammad
author_facet Aftab, Ayma
Afzal, Samia
Qamar, Zahida
Idrees, Muhammad
author_sort Aftab, Ayma
collection PubMed
description The result of improper treatment has led to the rise of Multidrug-resistant (MDR) strains. This concern still exists in Pakistan. In order to save energy, time and resources an early detection of resistant cases is imperative. Thus, a treated group of 100 isolates and a control group of 56 untreated isolates were studied. PCR and gene sequencing showed mutations at codon 531 and 513 in the rpoB gene. 12% of cases showed a double mutation in the rpoB gene. katG gene showed mutations at codon 315 and 299. 28.6% of the control group cases were positive for MDR whereas 100% of the treated group were positive for MDR. This study explores the significantly increasing ratio of MDR-TB among Pakistani population. This study provides prevalent MDR mutations among Pakistanis and suggests developing such molecular assays that are time and cost effective. Importance: Pakistan is a developing country and has fourth highest incidence rate of MDR-TB. The treatment of MDR-TB is the use of second line drugs that has severe side effects as well as it requires long time span. One of the strategies to control the spread of MDR-TB is to decipher the aberrations at molecular level in order to formulate potent drugs that can treat the patients within short span of time. Determining the mutation profile of MDR in Pakistani populations will open new horizons for the improvement of drug treatment regimens to make it more effective or for the development of novel potent drugs and vaccines to better treat the drug-resistant TB. Moreover, this study will be help in disease control program.
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spelling pubmed-83739712021-08-20 Early detection of MDR Mycobacterium tuberculosis mutations in Pakistan Aftab, Ayma Afzal, Samia Qamar, Zahida Idrees, Muhammad Sci Rep Article The result of improper treatment has led to the rise of Multidrug-resistant (MDR) strains. This concern still exists in Pakistan. In order to save energy, time and resources an early detection of resistant cases is imperative. Thus, a treated group of 100 isolates and a control group of 56 untreated isolates were studied. PCR and gene sequencing showed mutations at codon 531 and 513 in the rpoB gene. 12% of cases showed a double mutation in the rpoB gene. katG gene showed mutations at codon 315 and 299. 28.6% of the control group cases were positive for MDR whereas 100% of the treated group were positive for MDR. This study explores the significantly increasing ratio of MDR-TB among Pakistani population. This study provides prevalent MDR mutations among Pakistanis and suggests developing such molecular assays that are time and cost effective. Importance: Pakistan is a developing country and has fourth highest incidence rate of MDR-TB. The treatment of MDR-TB is the use of second line drugs that has severe side effects as well as it requires long time span. One of the strategies to control the spread of MDR-TB is to decipher the aberrations at molecular level in order to formulate potent drugs that can treat the patients within short span of time. Determining the mutation profile of MDR in Pakistani populations will open new horizons for the improvement of drug treatment regimens to make it more effective or for the development of novel potent drugs and vaccines to better treat the drug-resistant TB. Moreover, this study will be help in disease control program. Nature Publishing Group UK 2021-08-18 /pmc/articles/PMC8373971/ /pubmed/34408186 http://dx.doi.org/10.1038/s41598-021-96116-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Aftab, Ayma
Afzal, Samia
Qamar, Zahida
Idrees, Muhammad
Early detection of MDR Mycobacterium tuberculosis mutations in Pakistan
title Early detection of MDR Mycobacterium tuberculosis mutations in Pakistan
title_full Early detection of MDR Mycobacterium tuberculosis mutations in Pakistan
title_fullStr Early detection of MDR Mycobacterium tuberculosis mutations in Pakistan
title_full_unstemmed Early detection of MDR Mycobacterium tuberculosis mutations in Pakistan
title_short Early detection of MDR Mycobacterium tuberculosis mutations in Pakistan
title_sort early detection of mdr mycobacterium tuberculosis mutations in pakistan
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373971/
https://www.ncbi.nlm.nih.gov/pubmed/34408186
http://dx.doi.org/10.1038/s41598-021-96116-x
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