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Origin and Global Expansion of Mycobacterium tuberculosis Complex Lineage 3
SIMPLE SUMMARY: Tuberculosis still causes 1.5 million deaths annually and is mainly caused by Mycobacterium tuberculosis complex strains belonging to three evolutionary modern lineages (Lineages 2–4). While Lineage 2 and Lineage 4 virtually conquered the world, Lineage 3 is particularly successful i...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222951/ https://www.ncbi.nlm.nih.gov/pubmed/35741753 http://dx.doi.org/10.3390/genes13060990 |
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author | Shuaib, Yassir A. Utpatel, Christian Kohl, Thomas A. Barilar, Ivan Diricks, Margo Ashraf, Nadia Wieler, Lothar H. Kerubo, Glennah Mesfin, Eyob A. Diallo, Awa Ba Al-Hajoj, Sahal Ndung’u, Perpetua Fitzgibbon, Margaret M. Vaziri, Farzam Sintchenko, Vitali Martinez, Elena Viegas, Sofia O. Zhou, Yang Azmy, Aya Al-Amry, Khaled Godreuil, Sylvain Varma-Basil, Mandira Narang, Anshika Ali, Solomon Beckert, Patrick Dreyer, Viola Kabwe, Mwila Bates, Matthew Hoelscher, Michael Rachow, Andrea Gori, Andrea Tekwu, Emmanuel M. Sidze, Larissa K. Jean-Paul, Assam A. Beng, Veronique P. Ntoumi, Francine Frank, Matthias Diallo, Aissatou Gaye Mboup, Souleymane Tessema, Belay Beyene, Dereje Khan, Sadiq N. Diel, Roland Supply, Philip Maurer, Florian P. Hoffmann, Harald Niemann, Stefan Merker, Matthias |
author_facet | Shuaib, Yassir A. Utpatel, Christian Kohl, Thomas A. Barilar, Ivan Diricks, Margo Ashraf, Nadia Wieler, Lothar H. Kerubo, Glennah Mesfin, Eyob A. Diallo, Awa Ba Al-Hajoj, Sahal Ndung’u, Perpetua Fitzgibbon, Margaret M. Vaziri, Farzam Sintchenko, Vitali Martinez, Elena Viegas, Sofia O. Zhou, Yang Azmy, Aya Al-Amry, Khaled Godreuil, Sylvain Varma-Basil, Mandira Narang, Anshika Ali, Solomon Beckert, Patrick Dreyer, Viola Kabwe, Mwila Bates, Matthew Hoelscher, Michael Rachow, Andrea Gori, Andrea Tekwu, Emmanuel M. Sidze, Larissa K. Jean-Paul, Assam A. Beng, Veronique P. Ntoumi, Francine Frank, Matthias Diallo, Aissatou Gaye Mboup, Souleymane Tessema, Belay Beyene, Dereje Khan, Sadiq N. Diel, Roland Supply, Philip Maurer, Florian P. Hoffmann, Harald Niemann, Stefan Merker, Matthias |
author_sort | Shuaib, Yassir A. |
collection | PubMed |
description | SIMPLE SUMMARY: Tuberculosis still causes 1.5 million deaths annually and is mainly caused by Mycobacterium tuberculosis complex strains belonging to three evolutionary modern lineages (Lineages 2–4). While Lineage 2 and Lineage 4 virtually conquered the world, Lineage 3 is particularly successful in Northern and Eastern Africa, as well as in Southern Asia, the suspected evolutionary origin of these strains. Here, we sought to understand how Lineage 3 strains came to the African continent. To this end, we performed routine genotyping to characterize over 2500 clinical isolates from 38 countries. We then selected a representative collection of 373 isolates for a whole-genome analysis and a modeling approach to infer the geographic origin of different sublineages. In fact, the origin of Lineage 3 could be located in India, and we found evidence for independent introductions of four distinct sublineages into North/East Africa, in line with known ancient exchanges and migrations between both world regions. Our study illustrates that the evolutionary history of humans and their pathogens are closely connected and further provides a systematic understanding of the genomic diversity of Lineage 3, which could be important for the development of new tuberculosis vaccines or new therapeutics. ABSTRACT: Mycobacterium tuberculosis complex (MTBC) Lineage 3 (L3) strains are abundant in world regions with the highest tuberculosis burden. To investigate the population structure and the global diversity of this major lineage, we analyzed a dataset comprising 2682 L3 strains from 38 countries over 5 continents, by employing 24-loci mycobacterial interspersed repetitive unit-variable number of tandem repeats genotyping (MIRU-VNTR) and drug susceptibility testing. We further combined whole-genome sequencing (WGS) and phylogeographic analysis for 373 strains representing the global L3 genetic diversity. Ancestral state reconstruction confirmed that the origin of L3 strains is located in Southern Asia and further revealed multiple independent introduction events into North-East and East Africa. This study provides a systematic understanding of the global diversity of L3 strains and reports phylogenetic variations that could inform clinical trials which evaluate the effectivity of new drugs/regimens or vaccine candidates. |
format | Online Article Text |
id | pubmed-9222951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92229512022-06-24 Origin and Global Expansion of Mycobacterium tuberculosis Complex Lineage 3 Shuaib, Yassir A. Utpatel, Christian Kohl, Thomas A. Barilar, Ivan Diricks, Margo Ashraf, Nadia Wieler, Lothar H. Kerubo, Glennah Mesfin, Eyob A. Diallo, Awa Ba Al-Hajoj, Sahal Ndung’u, Perpetua Fitzgibbon, Margaret M. Vaziri, Farzam Sintchenko, Vitali Martinez, Elena Viegas, Sofia O. Zhou, Yang Azmy, Aya Al-Amry, Khaled Godreuil, Sylvain Varma-Basil, Mandira Narang, Anshika Ali, Solomon Beckert, Patrick Dreyer, Viola Kabwe, Mwila Bates, Matthew Hoelscher, Michael Rachow, Andrea Gori, Andrea Tekwu, Emmanuel M. Sidze, Larissa K. Jean-Paul, Assam A. Beng, Veronique P. Ntoumi, Francine Frank, Matthias Diallo, Aissatou Gaye Mboup, Souleymane Tessema, Belay Beyene, Dereje Khan, Sadiq N. Diel, Roland Supply, Philip Maurer, Florian P. Hoffmann, Harald Niemann, Stefan Merker, Matthias Genes (Basel) Article SIMPLE SUMMARY: Tuberculosis still causes 1.5 million deaths annually and is mainly caused by Mycobacterium tuberculosis complex strains belonging to three evolutionary modern lineages (Lineages 2–4). While Lineage 2 and Lineage 4 virtually conquered the world, Lineage 3 is particularly successful in Northern and Eastern Africa, as well as in Southern Asia, the suspected evolutionary origin of these strains. Here, we sought to understand how Lineage 3 strains came to the African continent. To this end, we performed routine genotyping to characterize over 2500 clinical isolates from 38 countries. We then selected a representative collection of 373 isolates for a whole-genome analysis and a modeling approach to infer the geographic origin of different sublineages. In fact, the origin of Lineage 3 could be located in India, and we found evidence for independent introductions of four distinct sublineages into North/East Africa, in line with known ancient exchanges and migrations between both world regions. Our study illustrates that the evolutionary history of humans and their pathogens are closely connected and further provides a systematic understanding of the genomic diversity of Lineage 3, which could be important for the development of new tuberculosis vaccines or new therapeutics. ABSTRACT: Mycobacterium tuberculosis complex (MTBC) Lineage 3 (L3) strains are abundant in world regions with the highest tuberculosis burden. To investigate the population structure and the global diversity of this major lineage, we analyzed a dataset comprising 2682 L3 strains from 38 countries over 5 continents, by employing 24-loci mycobacterial interspersed repetitive unit-variable number of tandem repeats genotyping (MIRU-VNTR) and drug susceptibility testing. We further combined whole-genome sequencing (WGS) and phylogeographic analysis for 373 strains representing the global L3 genetic diversity. Ancestral state reconstruction confirmed that the origin of L3 strains is located in Southern Asia and further revealed multiple independent introduction events into North-East and East Africa. This study provides a systematic understanding of the global diversity of L3 strains and reports phylogenetic variations that could inform clinical trials which evaluate the effectivity of new drugs/regimens or vaccine candidates. MDPI 2022-05-31 /pmc/articles/PMC9222951/ /pubmed/35741753 http://dx.doi.org/10.3390/genes13060990 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shuaib, Yassir A. Utpatel, Christian Kohl, Thomas A. Barilar, Ivan Diricks, Margo Ashraf, Nadia Wieler, Lothar H. Kerubo, Glennah Mesfin, Eyob A. Diallo, Awa Ba Al-Hajoj, Sahal Ndung’u, Perpetua Fitzgibbon, Margaret M. Vaziri, Farzam Sintchenko, Vitali Martinez, Elena Viegas, Sofia O. Zhou, Yang Azmy, Aya Al-Amry, Khaled Godreuil, Sylvain Varma-Basil, Mandira Narang, Anshika Ali, Solomon Beckert, Patrick Dreyer, Viola Kabwe, Mwila Bates, Matthew Hoelscher, Michael Rachow, Andrea Gori, Andrea Tekwu, Emmanuel M. Sidze, Larissa K. Jean-Paul, Assam A. Beng, Veronique P. Ntoumi, Francine Frank, Matthias Diallo, Aissatou Gaye Mboup, Souleymane Tessema, Belay Beyene, Dereje Khan, Sadiq N. Diel, Roland Supply, Philip Maurer, Florian P. Hoffmann, Harald Niemann, Stefan Merker, Matthias Origin and Global Expansion of Mycobacterium tuberculosis Complex Lineage 3 |
title | Origin and Global Expansion of Mycobacterium tuberculosis Complex Lineage 3 |
title_full | Origin and Global Expansion of Mycobacterium tuberculosis Complex Lineage 3 |
title_fullStr | Origin and Global Expansion of Mycobacterium tuberculosis Complex Lineage 3 |
title_full_unstemmed | Origin and Global Expansion of Mycobacterium tuberculosis Complex Lineage 3 |
title_short | Origin and Global Expansion of Mycobacterium tuberculosis Complex Lineage 3 |
title_sort | origin and global expansion of mycobacterium tuberculosis complex lineage 3 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222951/ https://www.ncbi.nlm.nih.gov/pubmed/35741753 http://dx.doi.org/10.3390/genes13060990 |
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