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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2008-09-01
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Series: | PLoS Pathogens |
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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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