Origin, spread and demography of the Mycobacterium tuberculosis complex.

The evolutionary timing and spread of the Mycobacterium tuberculosis complex (MTBC), one of the most successful groups of bacterial pathogens, remains largely unknown. Here, using mycobacterial tandem repeat sequences as genetic markers, we show that the MTBC consists of two independent clades, one...

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Main Authors: Thierry Wirth, Falk Hildebrand, Caroline Allix-Béguec, Florian Wölbeling, Tanja Kubica, Kristin Kremer, Dick van Soolingen, Sabine Rüsch-Gerdes, Camille Locht, Sylvain Brisse, Axel Meyer, Philip Supply, Stefan Niemann
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-09-01
Series:PLoS Pathogens
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18802459/?tool=EBI
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spelling doaj-e07bdcf35f844004a9c4e7c82e56c1c02021-04-21T16:58:17ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742008-09-0149e100016010.1371/journal.ppat.1000160Origin, spread and demography of the Mycobacterium tuberculosis complex.Thierry WirthFalk HildebrandCaroline Allix-BéguecFlorian WölbelingTanja KubicaKristin KremerDick van SoolingenSabine Rüsch-GerdesCamille LochtSylvain BrisseAxel MeyerPhilip SupplyStefan NiemannThe evolutionary timing and spread of the Mycobacterium tuberculosis complex (MTBC), one of the most successful groups of bacterial pathogens, remains largely unknown. Here, using mycobacterial tandem repeat sequences as genetic markers, we show that the MTBC consists of two independent clades, one composed exclusively of M. tuberculosis lineages from humans and the other composed of both animal and human isolates. The latter also likely derived from a human pathogenic lineage, supporting the hypothesis of an original human host. Using Bayesian statistics and experimental data on the variability of the mycobacterial markers in infected patients, we estimated the age of the MTBC at 40,000 years, coinciding with the expansion of "modern" human populations out of Africa. Furthermore, coalescence analysis revealed a strong and recent demographic expansion in almost all M. tuberculosis lineages, which coincides with the human population explosion over the last two centuries. These findings thus unveil the dynamic dimension of the association between human host and pathogen populations.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18802459/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Thierry Wirth
Falk Hildebrand
Caroline Allix-Béguec
Florian Wölbeling
Tanja Kubica
Kristin Kremer
Dick van Soolingen
Sabine Rüsch-Gerdes
Camille Locht
Sylvain Brisse
Axel Meyer
Philip Supply
Stefan Niemann
spellingShingle Thierry Wirth
Falk Hildebrand
Caroline Allix-Béguec
Florian Wölbeling
Tanja Kubica
Kristin Kremer
Dick van Soolingen
Sabine Rüsch-Gerdes
Camille Locht
Sylvain Brisse
Axel Meyer
Philip Supply
Stefan Niemann
Origin, spread and demography of the Mycobacterium tuberculosis complex.
PLoS Pathogens
author_facet Thierry Wirth
Falk Hildebrand
Caroline Allix-Béguec
Florian Wölbeling
Tanja Kubica
Kristin Kremer
Dick van Soolingen
Sabine Rüsch-Gerdes
Camille Locht
Sylvain Brisse
Axel Meyer
Philip Supply
Stefan Niemann
author_sort Thierry Wirth
title Origin, spread and demography of the Mycobacterium tuberculosis complex.
title_short Origin, spread and demography of the Mycobacterium tuberculosis complex.
title_full Origin, spread and demography of the Mycobacterium tuberculosis complex.
title_fullStr Origin, spread and demography of the Mycobacterium tuberculosis complex.
title_full_unstemmed Origin, spread and demography of the Mycobacterium tuberculosis complex.
title_sort origin, spread and demography of the mycobacterium tuberculosis complex.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2008-09-01
description The evolutionary timing and spread of the Mycobacterium tuberculosis complex (MTBC), one of the most successful groups of bacterial pathogens, remains largely unknown. Here, using mycobacterial tandem repeat sequences as genetic markers, we show that the MTBC consists of two independent clades, one composed exclusively of M. tuberculosis lineages from humans and the other composed of both animal and human isolates. The latter also likely derived from a human pathogenic lineage, supporting the hypothesis of an original human host. Using Bayesian statistics and experimental data on the variability of the mycobacterial markers in infected patients, we estimated the age of the MTBC at 40,000 years, coinciding with the expansion of "modern" human populations out of Africa. Furthermore, coalescence analysis revealed a strong and recent demographic expansion in almost all M. tuberculosis lineages, which coincides with the human population explosion over the last two centuries. These findings thus unveil the dynamic dimension of the association between human host and pathogen populations.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18802459/?tool=EBI
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