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Recent Acquisition of Helicobacter pylori by Baka Pygmies

Both anatomically modern humans and the gastric pathogen Helicobacter pylori originated in Africa, and both species have been associated for at least 100,000 years. Seven geographically distinct H. pylori populations exist, three of which are indigenous to Africa: hpAfrica1, hpAfrica2, and hpNEAfric...

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Autores principales: Nell, Sandra, Eibach, Daniel, Montano, Valeria, Maady, Ayas, Nkwescheu, Armand, Siri, Jose, Elamin, Wael F., Falush, Daniel, Linz, Bodo, Achtman, Mark, Moodley, Yoshan, Suerbaum, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777998/
https://www.ncbi.nlm.nih.gov/pubmed/24068950
http://dx.doi.org/10.1371/journal.pgen.1003775
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author Nell, Sandra
Eibach, Daniel
Montano, Valeria
Maady, Ayas
Nkwescheu, Armand
Siri, Jose
Elamin, Wael F.
Falush, Daniel
Linz, Bodo
Achtman, Mark
Moodley, Yoshan
Suerbaum, Sebastian
author_facet Nell, Sandra
Eibach, Daniel
Montano, Valeria
Maady, Ayas
Nkwescheu, Armand
Siri, Jose
Elamin, Wael F.
Falush, Daniel
Linz, Bodo
Achtman, Mark
Moodley, Yoshan
Suerbaum, Sebastian
author_sort Nell, Sandra
collection PubMed
description Both anatomically modern humans and the gastric pathogen Helicobacter pylori originated in Africa, and both species have been associated for at least 100,000 years. Seven geographically distinct H. pylori populations exist, three of which are indigenous to Africa: hpAfrica1, hpAfrica2, and hpNEAfrica. The oldest and most divergent population, hpAfrica2, evolved within San hunter-gatherers, who represent one of the deepest branches of the human population tree. Anticipating the presence of ancient H. pylori lineages within all hunter-gatherer populations, we investigated the prevalence and population structure of H. pylori within Baka Pygmies in Cameroon. Gastric biopsies were obtained by esophagogastroduodenoscopy from 77 Baka from two geographically separated populations, and from 101 non-Baka individuals from neighboring agriculturalist populations, and subsequently cultured for H. pylori. Unexpectedly, Baka Pygmies showed a significantly lower H. pylori infection rate (20.8%) than non-Baka (80.2%). We generated multilocus haplotypes for each H. pylori isolate by DNA sequencing, but were not able to identify Baka-specific lineages, and most isolates in our sample were assigned to hpNEAfrica or hpAfrica1. The population hpNEAfrica, a marker for the expansion of the Nilo-Saharan language family, was divided into East African and Central West African subpopulations. Similarly, a new hpAfrica1 subpopulation, identified mainly among Cameroonians, supports eastern and western expansions of Bantu languages. An age-structured transmission model shows that the low H. pylori prevalence among Baka Pygmies is achievable within the timeframe of a few hundred years and suggests that demographic factors such as small population size and unusually low life expectancy can lead to the eradication of H. pylori from individual human populations. The Baka were thus either H. pylori-free or lost their ancient lineages during past demographic fluctuations. Using coalescent simulations and phylogenetic inference, we show that Baka almost certainly acquired their extant H. pylori through secondary contact with their agriculturalist neighbors.
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spelling pubmed-37779982013-09-25 Recent Acquisition of Helicobacter pylori by Baka Pygmies Nell, Sandra Eibach, Daniel Montano, Valeria Maady, Ayas Nkwescheu, Armand Siri, Jose Elamin, Wael F. Falush, Daniel Linz, Bodo Achtman, Mark Moodley, Yoshan Suerbaum, Sebastian PLoS Genet Research Article Both anatomically modern humans and the gastric pathogen Helicobacter pylori originated in Africa, and both species have been associated for at least 100,000 years. Seven geographically distinct H. pylori populations exist, three of which are indigenous to Africa: hpAfrica1, hpAfrica2, and hpNEAfrica. The oldest and most divergent population, hpAfrica2, evolved within San hunter-gatherers, who represent one of the deepest branches of the human population tree. Anticipating the presence of ancient H. pylori lineages within all hunter-gatherer populations, we investigated the prevalence and population structure of H. pylori within Baka Pygmies in Cameroon. Gastric biopsies were obtained by esophagogastroduodenoscopy from 77 Baka from two geographically separated populations, and from 101 non-Baka individuals from neighboring agriculturalist populations, and subsequently cultured for H. pylori. Unexpectedly, Baka Pygmies showed a significantly lower H. pylori infection rate (20.8%) than non-Baka (80.2%). We generated multilocus haplotypes for each H. pylori isolate by DNA sequencing, but were not able to identify Baka-specific lineages, and most isolates in our sample were assigned to hpNEAfrica or hpAfrica1. The population hpNEAfrica, a marker for the expansion of the Nilo-Saharan language family, was divided into East African and Central West African subpopulations. Similarly, a new hpAfrica1 subpopulation, identified mainly among Cameroonians, supports eastern and western expansions of Bantu languages. An age-structured transmission model shows that the low H. pylori prevalence among Baka Pygmies is achievable within the timeframe of a few hundred years and suggests that demographic factors such as small population size and unusually low life expectancy can lead to the eradication of H. pylori from individual human populations. The Baka were thus either H. pylori-free or lost their ancient lineages during past demographic fluctuations. Using coalescent simulations and phylogenetic inference, we show that Baka almost certainly acquired their extant H. pylori through secondary contact with their agriculturalist neighbors. Public Library of Science 2013-09-19 /pmc/articles/PMC3777998/ /pubmed/24068950 http://dx.doi.org/10.1371/journal.pgen.1003775 Text en © 2013 Nell et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Nell, Sandra
Eibach, Daniel
Montano, Valeria
Maady, Ayas
Nkwescheu, Armand
Siri, Jose
Elamin, Wael F.
Falush, Daniel
Linz, Bodo
Achtman, Mark
Moodley, Yoshan
Suerbaum, Sebastian
Recent Acquisition of Helicobacter pylori by Baka Pygmies
title Recent Acquisition of Helicobacter pylori by Baka Pygmies
title_full Recent Acquisition of Helicobacter pylori by Baka Pygmies
title_fullStr Recent Acquisition of Helicobacter pylori by Baka Pygmies
title_full_unstemmed Recent Acquisition of Helicobacter pylori by Baka Pygmies
title_short Recent Acquisition of Helicobacter pylori by Baka Pygmies
title_sort recent acquisition of helicobacter pylori by baka pygmies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777998/
https://www.ncbi.nlm.nih.gov/pubmed/24068950
http://dx.doi.org/10.1371/journal.pgen.1003775
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