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The Macaque Gut Microbiome in Health, Lentiviral Infection, and Chronic Enterocolitis

The vertebrate gut harbors a vast community of bacterial mutualists, the composition of which is modulated by the host immune system. Many gastrointestinal (GI) diseases are expected to be associated with disruptions of host-bacterial interactions, but relatively few comprehensive studies have been...

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Autores principales: McKenna, Philip, Hoffmann, Christian, Minkah, Nana, Aye, Pyone Pyone, Lackner, Andrew, Liu, Zongzhi, Lozupone, Catherine A, Hamady, Micah, Knight, Rob, Bushman, Frederic D
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2222957/
https://www.ncbi.nlm.nih.gov/pubmed/18248093
http://dx.doi.org/10.1371/journal.ppat.0040020
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author McKenna, Philip
Hoffmann, Christian
Minkah, Nana
Aye, Pyone Pyone
Lackner, Andrew
Liu, Zongzhi
Lozupone, Catherine A
Hamady, Micah
Knight, Rob
Bushman, Frederic D
author_facet McKenna, Philip
Hoffmann, Christian
Minkah, Nana
Aye, Pyone Pyone
Lackner, Andrew
Liu, Zongzhi
Lozupone, Catherine A
Hamady, Micah
Knight, Rob
Bushman, Frederic D
author_sort McKenna, Philip
collection PubMed
description The vertebrate gut harbors a vast community of bacterial mutualists, the composition of which is modulated by the host immune system. Many gastrointestinal (GI) diseases are expected to be associated with disruptions of host-bacterial interactions, but relatively few comprehensive studies have been reported. We have used the rhesus macaque model to investigate forces shaping GI bacterial communities. We used DNA bar coding and pyrosequencing to characterize 141,000 sequences of 16S rRNA genes obtained from 100 uncultured GI bacterial samples, allowing quantitative analysis of community composition in health and disease. Microbial communities of macaques were distinct from those of mice and humans in both abundance and types of taxa present. The macaque communities differed among samples from intestinal mucosa, colonic contents, and stool, paralleling studies of humans. Communities also differed among animals, over time within individual animals, and between males and females. To investigate changes associated with disease, samples of colonic contents taken at necropsy were compared between healthy animals and animals with colitis and undergoing antibiotic therapy. Communities from diseased and healthy animals also differed significantly in composition. This work provides comprehensive data and improved methods for studying the role of commensal microbiota in macaque models of GI diseases and provides a model for the large-scale screening of the human gut microbiome.
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spelling pubmed-22229572008-02-01 The Macaque Gut Microbiome in Health, Lentiviral Infection, and Chronic Enterocolitis McKenna, Philip Hoffmann, Christian Minkah, Nana Aye, Pyone Pyone Lackner, Andrew Liu, Zongzhi Lozupone, Catherine A Hamady, Micah Knight, Rob Bushman, Frederic D PLoS Pathog Research Article The vertebrate gut harbors a vast community of bacterial mutualists, the composition of which is modulated by the host immune system. Many gastrointestinal (GI) diseases are expected to be associated with disruptions of host-bacterial interactions, but relatively few comprehensive studies have been reported. We have used the rhesus macaque model to investigate forces shaping GI bacterial communities. We used DNA bar coding and pyrosequencing to characterize 141,000 sequences of 16S rRNA genes obtained from 100 uncultured GI bacterial samples, allowing quantitative analysis of community composition in health and disease. Microbial communities of macaques were distinct from those of mice and humans in both abundance and types of taxa present. The macaque communities differed among samples from intestinal mucosa, colonic contents, and stool, paralleling studies of humans. Communities also differed among animals, over time within individual animals, and between males and females. To investigate changes associated with disease, samples of colonic contents taken at necropsy were compared between healthy animals and animals with colitis and undergoing antibiotic therapy. Communities from diseased and healthy animals also differed significantly in composition. This work provides comprehensive data and improved methods for studying the role of commensal microbiota in macaque models of GI diseases and provides a model for the large-scale screening of the human gut microbiome. Public Library of Science 2008-02 2008-02-01 /pmc/articles/PMC2222957/ /pubmed/18248093 http://dx.doi.org/10.1371/journal.ppat.0040020 Text en © 2008 McKenna 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
McKenna, Philip
Hoffmann, Christian
Minkah, Nana
Aye, Pyone Pyone
Lackner, Andrew
Liu, Zongzhi
Lozupone, Catherine A
Hamady, Micah
Knight, Rob
Bushman, Frederic D
The Macaque Gut Microbiome in Health, Lentiviral Infection, and Chronic Enterocolitis
title The Macaque Gut Microbiome in Health, Lentiviral Infection, and Chronic Enterocolitis
title_full The Macaque Gut Microbiome in Health, Lentiviral Infection, and Chronic Enterocolitis
title_fullStr The Macaque Gut Microbiome in Health, Lentiviral Infection, and Chronic Enterocolitis
title_full_unstemmed The Macaque Gut Microbiome in Health, Lentiviral Infection, and Chronic Enterocolitis
title_short The Macaque Gut Microbiome in Health, Lentiviral Infection, and Chronic Enterocolitis
title_sort macaque gut microbiome in health, lentiviral infection, and chronic enterocolitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2222957/
https://www.ncbi.nlm.nih.gov/pubmed/18248093
http://dx.doi.org/10.1371/journal.ppat.0040020
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