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Whole genome analysis of extensively drug resistant Mycobacterium tuberculosis strains in Peru

Peru has the highest burden of multidrug-resistant tuberculosis in the Americas region. Since 1999, the annual number of extensively drug-resistant tuberculosis (XDR-TB) Peruvian cases has been increasing, becoming a public health challenge. The objective of this study was to perform genomic charact...

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Autores principales: Santos-Lazaro, David, Gavilan, Ronnie G., Solari, Lely, Vigo, Aiko N., Puyen, Zully M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097007/
https://www.ncbi.nlm.nih.gov/pubmed/33947918
http://dx.doi.org/10.1038/s41598-021-88603-y
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author Santos-Lazaro, David
Gavilan, Ronnie G.
Solari, Lely
Vigo, Aiko N.
Puyen, Zully M.
author_facet Santos-Lazaro, David
Gavilan, Ronnie G.
Solari, Lely
Vigo, Aiko N.
Puyen, Zully M.
author_sort Santos-Lazaro, David
collection PubMed
description Peru has the highest burden of multidrug-resistant tuberculosis in the Americas region. Since 1999, the annual number of extensively drug-resistant tuberculosis (XDR-TB) Peruvian cases has been increasing, becoming a public health challenge. The objective of this study was to perform genomic characterization of Mycobacterium tuberculosis strains obtained from Peruvian patients with XDR-TB diagnosed from 2011 to 2015 in Peru. Whole genome sequencing (WGS) was performed on 68 XDR-TB strains from different regions of Peru. 58 (85.3%) strains came from the most populated districts of Lima and Callao. Concerning the lineages, 62 (91.2%) strains belonged to the Euro-American Lineage, while the remaining 6 (8.8%) strains belonged to the East-Asian Lineage. Most strains (90%) had high-confidence resistance mutations according to pre-established WHO-confident grading system. Discordant results between microbiological and molecular methodologies were caused by mutations outside the hotspot regions analysed by commercial molecular assays (rpoB I491F and inhA S94A). Cluster analysis using a cut-off ≤ 10 SNPs revealed that only 23 (34%) strains evidenced recent transmission links. This study highlights the relevance and utility of WGS as a high-resolution approach to predict drug resistance, analyse transmission of strains between groups, and determine evolutionary patterns of circulating XDR-TB strains in the country.
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spelling pubmed-80970072021-05-05 Whole genome analysis of extensively drug resistant Mycobacterium tuberculosis strains in Peru Santos-Lazaro, David Gavilan, Ronnie G. Solari, Lely Vigo, Aiko N. Puyen, Zully M. Sci Rep Article Peru has the highest burden of multidrug-resistant tuberculosis in the Americas region. Since 1999, the annual number of extensively drug-resistant tuberculosis (XDR-TB) Peruvian cases has been increasing, becoming a public health challenge. The objective of this study was to perform genomic characterization of Mycobacterium tuberculosis strains obtained from Peruvian patients with XDR-TB diagnosed from 2011 to 2015 in Peru. Whole genome sequencing (WGS) was performed on 68 XDR-TB strains from different regions of Peru. 58 (85.3%) strains came from the most populated districts of Lima and Callao. Concerning the lineages, 62 (91.2%) strains belonged to the Euro-American Lineage, while the remaining 6 (8.8%) strains belonged to the East-Asian Lineage. Most strains (90%) had high-confidence resistance mutations according to pre-established WHO-confident grading system. Discordant results between microbiological and molecular methodologies were caused by mutations outside the hotspot regions analysed by commercial molecular assays (rpoB I491F and inhA S94A). Cluster analysis using a cut-off ≤ 10 SNPs revealed that only 23 (34%) strains evidenced recent transmission links. This study highlights the relevance and utility of WGS as a high-resolution approach to predict drug resistance, analyse transmission of strains between groups, and determine evolutionary patterns of circulating XDR-TB strains in the country. Nature Publishing Group UK 2021-05-04 /pmc/articles/PMC8097007/ /pubmed/33947918 http://dx.doi.org/10.1038/s41598-021-88603-y 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
Santos-Lazaro, David
Gavilan, Ronnie G.
Solari, Lely
Vigo, Aiko N.
Puyen, Zully M.
Whole genome analysis of extensively drug resistant Mycobacterium tuberculosis strains in Peru
title Whole genome analysis of extensively drug resistant Mycobacterium tuberculosis strains in Peru
title_full Whole genome analysis of extensively drug resistant Mycobacterium tuberculosis strains in Peru
title_fullStr Whole genome analysis of extensively drug resistant Mycobacterium tuberculosis strains in Peru
title_full_unstemmed Whole genome analysis of extensively drug resistant Mycobacterium tuberculosis strains in Peru
title_short Whole genome analysis of extensively drug resistant Mycobacterium tuberculosis strains in Peru
title_sort whole genome analysis of extensively drug resistant mycobacterium tuberculosis strains in peru
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097007/
https://www.ncbi.nlm.nih.gov/pubmed/33947918
http://dx.doi.org/10.1038/s41598-021-88603-y
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