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Evidence for Host-Bacterial Co-evolution via Genome Sequence Analysis of 480 Thai Mycobacterium tuberculosis Lineage 1 Isolates

Tuberculosis presents a global health challenge. Mycobacterium tuberculosis is divided into several lineages, each with a different geographical distribution. M. tuberculosis lineage 1 (L1) is common in the high-burden areas in East Africa and Southeast Asia. Although the founder effect contributes...

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Autores principales: Palittapongarnpim, Prasit, Ajawatanawong, Pravech, Viratyosin, Wasna, Smittipat, Nat, Disratthakit, Areeya, Mahasirimongkol, Surakameth, Yanai, Hideki, Yamada, Norio, Nedsuwan, Supalert, Imasanguan, Worarat, Kantipong, Pacharee, Chaiyasirinroje, Boonchai, Wongyai, Jiraporn, Toyo-oka, Licht, Phelan, Jody, Parkhill, Julian, Clark, Taane G., Hibberd, Martin L., Ruengchai, Wuthiwat, Palittapongarnpim, Panawun, Juthayothin, Tada, Tongsima, Sissades, Tokunaga, Katsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072702/
https://www.ncbi.nlm.nih.gov/pubmed/30072734
http://dx.doi.org/10.1038/s41598-018-29986-3
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author Palittapongarnpim, Prasit
Ajawatanawong, Pravech
Viratyosin, Wasna
Smittipat, Nat
Disratthakit, Areeya
Mahasirimongkol, Surakameth
Yanai, Hideki
Yamada, Norio
Nedsuwan, Supalert
Imasanguan, Worarat
Kantipong, Pacharee
Chaiyasirinroje, Boonchai
Wongyai, Jiraporn
Toyo-oka, Licht
Phelan, Jody
Parkhill, Julian
Clark, Taane G.
Hibberd, Martin L.
Ruengchai, Wuthiwat
Palittapongarnpim, Panawun
Juthayothin, Tada
Tongsima, Sissades
Tokunaga, Katsushi
author_facet Palittapongarnpim, Prasit
Ajawatanawong, Pravech
Viratyosin, Wasna
Smittipat, Nat
Disratthakit, Areeya
Mahasirimongkol, Surakameth
Yanai, Hideki
Yamada, Norio
Nedsuwan, Supalert
Imasanguan, Worarat
Kantipong, Pacharee
Chaiyasirinroje, Boonchai
Wongyai, Jiraporn
Toyo-oka, Licht
Phelan, Jody
Parkhill, Julian
Clark, Taane G.
Hibberd, Martin L.
Ruengchai, Wuthiwat
Palittapongarnpim, Panawun
Juthayothin, Tada
Tongsima, Sissades
Tokunaga, Katsushi
author_sort Palittapongarnpim, Prasit
collection PubMed
description Tuberculosis presents a global health challenge. Mycobacterium tuberculosis is divided into several lineages, each with a different geographical distribution. M. tuberculosis lineage 1 (L1) is common in the high-burden areas in East Africa and Southeast Asia. Although the founder effect contributes significantly to the phylogeographic profile, co-evolution between the host and M. tuberculosis may also play a role. Here, we reported the genomic analysis of 480 L1 isolates from patients in northern Thailand. The studied bacterial population was genetically diverse, allowing the identification of a total of 18 sublineages distributed into three major clades. The majority of isolates belonged to L1.1 followed by L1.2.1 and L1.2.2. Comparison of the single nucleotide variant (SNV) phylogenetic tree and the clades defined by spoligotyping revealed some monophyletic clades representing EAI2_MNL, EAI2_NTM and EAI6_BGD1 spoligotypes. Our work demonstrates that ambiguity in spoligotype assignment could be partially resolved if the entire DR region is investigated. Using the information to map L1 diversity across Southeast Asia highlighted differences in the dominant strain-types in each individual country, despite extensive interactions between populations over time. This finding supported the hypothesis that there is co-evolution between the bacteria and the host, and have implications for tuberculosis disease control.
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spelling pubmed-60727022018-08-06 Evidence for Host-Bacterial Co-evolution via Genome Sequence Analysis of 480 Thai Mycobacterium tuberculosis Lineage 1 Isolates Palittapongarnpim, Prasit Ajawatanawong, Pravech Viratyosin, Wasna Smittipat, Nat Disratthakit, Areeya Mahasirimongkol, Surakameth Yanai, Hideki Yamada, Norio Nedsuwan, Supalert Imasanguan, Worarat Kantipong, Pacharee Chaiyasirinroje, Boonchai Wongyai, Jiraporn Toyo-oka, Licht Phelan, Jody Parkhill, Julian Clark, Taane G. Hibberd, Martin L. Ruengchai, Wuthiwat Palittapongarnpim, Panawun Juthayothin, Tada Tongsima, Sissades Tokunaga, Katsushi Sci Rep Article Tuberculosis presents a global health challenge. Mycobacterium tuberculosis is divided into several lineages, each with a different geographical distribution. M. tuberculosis lineage 1 (L1) is common in the high-burden areas in East Africa and Southeast Asia. Although the founder effect contributes significantly to the phylogeographic profile, co-evolution between the host and M. tuberculosis may also play a role. Here, we reported the genomic analysis of 480 L1 isolates from patients in northern Thailand. The studied bacterial population was genetically diverse, allowing the identification of a total of 18 sublineages distributed into three major clades. The majority of isolates belonged to L1.1 followed by L1.2.1 and L1.2.2. Comparison of the single nucleotide variant (SNV) phylogenetic tree and the clades defined by spoligotyping revealed some monophyletic clades representing EAI2_MNL, EAI2_NTM and EAI6_BGD1 spoligotypes. Our work demonstrates that ambiguity in spoligotype assignment could be partially resolved if the entire DR region is investigated. Using the information to map L1 diversity across Southeast Asia highlighted differences in the dominant strain-types in each individual country, despite extensive interactions between populations over time. This finding supported the hypothesis that there is co-evolution between the bacteria and the host, and have implications for tuberculosis disease control. Nature Publishing Group UK 2018-08-02 /pmc/articles/PMC6072702/ /pubmed/30072734 http://dx.doi.org/10.1038/s41598-018-29986-3 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Palittapongarnpim, Prasit
Ajawatanawong, Pravech
Viratyosin, Wasna
Smittipat, Nat
Disratthakit, Areeya
Mahasirimongkol, Surakameth
Yanai, Hideki
Yamada, Norio
Nedsuwan, Supalert
Imasanguan, Worarat
Kantipong, Pacharee
Chaiyasirinroje, Boonchai
Wongyai, Jiraporn
Toyo-oka, Licht
Phelan, Jody
Parkhill, Julian
Clark, Taane G.
Hibberd, Martin L.
Ruengchai, Wuthiwat
Palittapongarnpim, Panawun
Juthayothin, Tada
Tongsima, Sissades
Tokunaga, Katsushi
Evidence for Host-Bacterial Co-evolution via Genome Sequence Analysis of 480 Thai Mycobacterium tuberculosis Lineage 1 Isolates
title Evidence for Host-Bacterial Co-evolution via Genome Sequence Analysis of 480 Thai Mycobacterium tuberculosis Lineage 1 Isolates
title_full Evidence for Host-Bacterial Co-evolution via Genome Sequence Analysis of 480 Thai Mycobacterium tuberculosis Lineage 1 Isolates
title_fullStr Evidence for Host-Bacterial Co-evolution via Genome Sequence Analysis of 480 Thai Mycobacterium tuberculosis Lineage 1 Isolates
title_full_unstemmed Evidence for Host-Bacterial Co-evolution via Genome Sequence Analysis of 480 Thai Mycobacterium tuberculosis Lineage 1 Isolates
title_short Evidence for Host-Bacterial Co-evolution via Genome Sequence Analysis of 480 Thai Mycobacterium tuberculosis Lineage 1 Isolates
title_sort evidence for host-bacterial co-evolution via genome sequence analysis of 480 thai mycobacterium tuberculosis lineage 1 isolates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072702/
https://www.ncbi.nlm.nih.gov/pubmed/30072734
http://dx.doi.org/10.1038/s41598-018-29986-3
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