Whole Genome Sequencing of Mycobacterium tuberculosis under routine conditions in a high-burden area of multidrug-resistant tuberculosis in Peru

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Whole Genome Sequencing (WGS) is a promising tool in the global fight against tuberculosis (TB). The aim of this study was to evaluate the use of WGS in routine conditions for detection of drug resistance markers and transmission clusters in a multidrug-resistant TB hot-spot area in Peru. For this,...

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Detalles Bibliográficos
Autores: Puyén, Zully M., Santos-Lázaro, David, Vigo, Aiko N., Cotrina, Vidia V., Ruiz-Nizama, Nathaly, Alarcón, Miriam J., Asto, Belisa, Huamán, Teresa, Moore, David A.J.
Formato: artículo
Fecha de Publicación:2024
Institución:Universidad Peruana de Ciencias Aplicadas
Repositorio:UPC-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorioacademico.upc.edu.pe:10757/675817
Enlace del recurso:http://hdl.handle.net/10757/675817
Nivel de acceso:acceso abierto
Materia:Antitubercular Agents
Drug Resistance
Multiple, Bacterial
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dc.title.es_PE.fl_str_mv Whole Genome Sequencing of Mycobacterium tuberculosis under routine conditions in a high-burden area of multidrug-resistant tuberculosis in Peru
title Whole Genome Sequencing of Mycobacterium tuberculosis under routine conditions in a high-burden area of multidrug-resistant tuberculosis in Peru
spellingShingle Whole Genome Sequencing of Mycobacterium tuberculosis under routine conditions in a high-burden area of multidrug-resistant tuberculosis in Peru
Puyén, Zully M.
Antitubercular Agents
Drug Resistance
Multiple, Bacterial
title_short Whole Genome Sequencing of Mycobacterium tuberculosis under routine conditions in a high-burden area of multidrug-resistant tuberculosis in Peru
title_full Whole Genome Sequencing of Mycobacterium tuberculosis under routine conditions in a high-burden area of multidrug-resistant tuberculosis in Peru
title_fullStr Whole Genome Sequencing of Mycobacterium tuberculosis under routine conditions in a high-burden area of multidrug-resistant tuberculosis in Peru
title_full_unstemmed Whole Genome Sequencing of Mycobacterium tuberculosis under routine conditions in a high-burden area of multidrug-resistant tuberculosis in Peru
title_sort Whole Genome Sequencing of Mycobacterium tuberculosis under routine conditions in a high-burden area of multidrug-resistant tuberculosis in Peru
author Puyén, Zully M.
author_facet Puyén, Zully M.
Santos-Lázaro, David
Vigo, Aiko N.
Cotrina, Vidia V.
Ruiz-Nizama, Nathaly
Alarcón, Miriam J.
Asto, Belisa
Huamán, Teresa
Moore, David A.J.
author_role author
author2 Santos-Lázaro, David
Vigo, Aiko N.
Cotrina, Vidia V.
Ruiz-Nizama, Nathaly
Alarcón, Miriam J.
Asto, Belisa
Huamán, Teresa
Moore, David A.J.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Puyén, Zully M.
Santos-Lázaro, David
Vigo, Aiko N.
Cotrina, Vidia V.
Ruiz-Nizama, Nathaly
Alarcón, Miriam J.
Asto, Belisa
Huamán, Teresa
Moore, David A.J.
dc.subject.es_PE.fl_str_mv Antitubercular Agents
Drug Resistance
Multiple, Bacterial
topic Antitubercular Agents
Drug Resistance
Multiple, Bacterial
description Whole Genome Sequencing (WGS) is a promising tool in the global fight against tuberculosis (TB). The aim of this study was to evaluate the use of WGS in routine conditions for detection of drug resistance markers and transmission clusters in a multidrug-resistant TB hot-spot area in Peru. For this, 140 drug-resistant Mycobacterium tuberculosis strains from Lima and Callao were prospectively selected and processed through routine (GenoType MTBDRsl and BACTEC MGIT) and WGS workflows, simultaneously. Resistance was determined in accordance with the World Health Organization mutation catalogue. Agreements between WGS and BACTEC results were calculated for rifampicin, isoniazid, pyrazinamide, moxifloxacin, levofloxacin, amikacin and capreomycin. Transmission clusters were determined using different cut-off values of Single Nucleotide Polymorphism differences. 100% (140/140) of strains had valid WGS results for 13 anti-TB drugs. However, the availability of final, definitive phenotypic BACTEC MGIT results varied by drug with 10–17% of invalid results for the seven compared drugs. The median time to obtain results of WGS for the complete set of drugs was 11.5 days, compared to 28.6–52.6 days for the routine workflow. Overall categorical agreement by WGS and BACTEC MGIT for the compared drugs was 96.5%. Kappa index was good (0.65≤k≤1.00), except for moxifloxacin, but the sensitivity and specificity values were high for all cases. 97.9% (137/140) of strains were characterized with only one sublineage (134 belonging to “lineage 4” and 3 to “lineage 2”), and 2.1% (3/ 140) were mixed strains presenting two different sublineages. Clustering rates of 3.6% (5/ 140), 17.9% (25/140) and 22.1% (31/140) were obtained for 5, 10 and 12 SNP cut-off values, respectively. In conclusion, routine WGS has a high diagnostic accuracy to detect resistance against key current anti-TB drugs, allowing results to be obtained through a single analysis and helping to cut quickly the chain of transmission of drug-resistant TB in Peru.
publishDate 2024
dc.date.accessioned.none.fl_str_mv 2024-09-22T12:59:05Z
dc.date.available.none.fl_str_mv 2024-09-22T12:59:05Z
dc.date.issued.fl_str_mv 2024-06-01
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dc.identifier.doi.none.fl_str_mv 10.1371/journal.pone.0304130
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10757/675817
dc.identifier.eissn.none.fl_str_mv 19326203
dc.identifier.journal.es_PE.fl_str_mv PLoS ONE
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dc.publisher.es_PE.fl_str_mv Public Library of Science
dc.source.es_PE.fl_str_mv Universidad Peruana de Ciencias Aplicadas (UPC)
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dc.source.journaltitle.none.fl_str_mv PLoS ONE
dc.source.volume.none.fl_str_mv 19
dc.source.issue.none.fl_str_mv 6 June
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For this, 140 drug-resistant Mycobacterium tuberculosis strains from Lima and Callao were prospectively selected and processed through routine (GenoType MTBDRsl and BACTEC MGIT) and WGS workflows, simultaneously. Resistance was determined in accordance with the World Health Organization mutation catalogue. Agreements between WGS and BACTEC results were calculated for rifampicin, isoniazid, pyrazinamide, moxifloxacin, levofloxacin, amikacin and capreomycin. Transmission clusters were determined using different cut-off values of Single Nucleotide Polymorphism differences. 100% (140/140) of strains had valid WGS results for 13 anti-TB drugs. However, the availability of final, definitive phenotypic BACTEC MGIT results varied by drug with 10–17% of invalid results for the seven compared drugs. The median time to obtain results of WGS for the complete set of drugs was 11.5 days, compared to 28.6–52.6 days for the routine workflow. 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