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Prevalence of mutations in genes associated with rifampicin and isoniazid resistance in Mycobacterium tuberculosis clinical isolates

Purpose: To analyze prevalence of mutations in genes associated with rifampicin and isoniazid resistance in Mycobacterium tuberculosis clinical isolates from patients with possible MDR TB of Puducherry, South India and to explore the association of specific mutations conferring rifampicin (RIF) resi...

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Autores principales: Muthaiah, Muthuraj, Shivekar, Smita Sunil, Cuppusamy Kapalamurthy, Vidya Raj, Alagappan, Chitra, Sakkaravarthy, Anbazhagi, Brammachary, Usharani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850230/
https://www.ncbi.nlm.nih.gov/pubmed/31723707
http://dx.doi.org/10.1016/j.jctube.2017.06.001
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author Muthaiah, Muthuraj
Shivekar, Smita Sunil
Cuppusamy Kapalamurthy, Vidya Raj
Alagappan, Chitra
Sakkaravarthy, Anbazhagi
Brammachary, Usharani
author_facet Muthaiah, Muthuraj
Shivekar, Smita Sunil
Cuppusamy Kapalamurthy, Vidya Raj
Alagappan, Chitra
Sakkaravarthy, Anbazhagi
Brammachary, Usharani
author_sort Muthaiah, Muthuraj
collection PubMed
description Purpose: To analyze prevalence of mutations in genes associated with rifampicin and isoniazid resistance in Mycobacterium tuberculosis clinical isolates from patients with possible MDR TB of Puducherry, South India and to explore the association of specific mutations conferring rifampicin (RIF) resistance. Methods: We performed a commercial Genotype MDBDRplus V.2.0 assay for the rapid detection of rifampicin and isoniazid resistance directly on sputum specimens of patients with possible MDR TB. Results: Totally 558 multidrug resistant, 293 RIF mono resistant and 923 INH mono resistant tuberculosis were detected from the 12,786 patients with possible MDR TB samples. The 50.5% mutations were observed in the region of S531L in MDR TB patients and 55.6% in rifampicin monoresistant cases. In total isoniazid monoresistant, 68.0% mutations were detected in katG gene, which is more prevalent in comparison to inhA gene 32.0%. There were about 57.9% and 32.2% MDR TB cases diagnosed in the age group of > 15 to ≤ 45 years and > 45 to ≤ 60 years respectively. Conclusions: The rate of occurrences of mutations were found widely in the Rifampicin Resistant Determination Region (81 bp) of rpoB gene and the hypervariable region 530–533 codons of rpoB gene is alarming in the specification. The higher frequency of mutation in codons of rpoB (S531L) and katG (S315T) gene help to design simple, new and less expensive molecular techniques to use in peripheral laboratories.
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spelling pubmed-68502302019-11-13 Prevalence of mutations in genes associated with rifampicin and isoniazid resistance in Mycobacterium tuberculosis clinical isolates Muthaiah, Muthuraj Shivekar, Smita Sunil Cuppusamy Kapalamurthy, Vidya Raj Alagappan, Chitra Sakkaravarthy, Anbazhagi Brammachary, Usharani J Clin Tuberc Other Mycobact Dis Article Purpose: To analyze prevalence of mutations in genes associated with rifampicin and isoniazid resistance in Mycobacterium tuberculosis clinical isolates from patients with possible MDR TB of Puducherry, South India and to explore the association of specific mutations conferring rifampicin (RIF) resistance. Methods: We performed a commercial Genotype MDBDRplus V.2.0 assay for the rapid detection of rifampicin and isoniazid resistance directly on sputum specimens of patients with possible MDR TB. Results: Totally 558 multidrug resistant, 293 RIF mono resistant and 923 INH mono resistant tuberculosis were detected from the 12,786 patients with possible MDR TB samples. The 50.5% mutations were observed in the region of S531L in MDR TB patients and 55.6% in rifampicin monoresistant cases. In total isoniazid monoresistant, 68.0% mutations were detected in katG gene, which is more prevalent in comparison to inhA gene 32.0%. There were about 57.9% and 32.2% MDR TB cases diagnosed in the age group of > 15 to ≤ 45 years and > 45 to ≤ 60 years respectively. Conclusions: The rate of occurrences of mutations were found widely in the Rifampicin Resistant Determination Region (81 bp) of rpoB gene and the hypervariable region 530–533 codons of rpoB gene is alarming in the specification. The higher frequency of mutation in codons of rpoB (S531L) and katG (S315T) gene help to design simple, new and less expensive molecular techniques to use in peripheral laboratories. Elsevier 2017-06-20 /pmc/articles/PMC6850230/ /pubmed/31723707 http://dx.doi.org/10.1016/j.jctube.2017.06.001 Text en © 2017 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Muthaiah, Muthuraj
Shivekar, Smita Sunil
Cuppusamy Kapalamurthy, Vidya Raj
Alagappan, Chitra
Sakkaravarthy, Anbazhagi
Brammachary, Usharani
Prevalence of mutations in genes associated with rifampicin and isoniazid resistance in Mycobacterium tuberculosis clinical isolates
title Prevalence of mutations in genes associated with rifampicin and isoniazid resistance in Mycobacterium tuberculosis clinical isolates
title_full Prevalence of mutations in genes associated with rifampicin and isoniazid resistance in Mycobacterium tuberculosis clinical isolates
title_fullStr Prevalence of mutations in genes associated with rifampicin and isoniazid resistance in Mycobacterium tuberculosis clinical isolates
title_full_unstemmed Prevalence of mutations in genes associated with rifampicin and isoniazid resistance in Mycobacterium tuberculosis clinical isolates
title_short Prevalence of mutations in genes associated with rifampicin and isoniazid resistance in Mycobacterium tuberculosis clinical isolates
title_sort prevalence of mutations in genes associated with rifampicin and isoniazid resistance in mycobacterium tuberculosis clinical isolates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850230/
https://www.ncbi.nlm.nih.gov/pubmed/31723707
http://dx.doi.org/10.1016/j.jctube.2017.06.001
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