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Identifying genomic and metabolic features that can underlie early successional and opportunistic lifestyles of human gut symbionts
We lack a deep understanding of genetic and metabolic attributes specializing in microbial consortia for initial and subsequent waves of colonization of our body habitats. Here we show that phylogenetically interspersed bacteria in Clostridium cluster XIVa, an abundant group of bacteria in the adult...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460192/ https://www.ncbi.nlm.nih.gov/pubmed/22665442 http://dx.doi.org/10.1101/gr.138198.112 |
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author | Lozupone, Catherine Faust, Karoline Raes, Jeroen Faith, Jeremiah J. Frank, Daniel N. Zaneveld, Jesse Gordon, Jeffrey I. Knight, Rob |
author_facet | Lozupone, Catherine Faust, Karoline Raes, Jeroen Faith, Jeremiah J. Frank, Daniel N. Zaneveld, Jesse Gordon, Jeffrey I. Knight, Rob |
author_sort | Lozupone, Catherine |
collection | PubMed |
description | We lack a deep understanding of genetic and metabolic attributes specializing in microbial consortia for initial and subsequent waves of colonization of our body habitats. Here we show that phylogenetically interspersed bacteria in Clostridium cluster XIVa, an abundant group of bacteria in the adult human gut also known as the Clostridium coccoides or Eubacterium rectale group, contains species that have evolved distribution patterns consistent with either early successional or stable gut communities. The species that specialize to the infant gut are more likely to associate with systemic infections and can reach high abundances in individuals with Inflammatory Bowel Disease (IBD), indicating that a subset of the microbiota that have adapted to pioneer/opportunistic lifestyles may do well in both early development and with disease. We identified genes likely selected during adaptation to pioneer/opportunistic lifestyles as those for which early succession association and not phylogenetic relationships explain genomic abundance. These genes reveal potential mechanisms by which opportunistic gut bacteria tolerate osmotic and oxidative stress and potentially important aspects of their metabolism. These genes may not only be biomarkers of properties associated with adaptation to early succession and disturbance, but also leads for developing therapies aimed at promoting reestablishment of stable gut communities following physiologic or pathologic disturbances. |
format | Online Article Text |
id | pubmed-3460192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-34601922012-10-06 Identifying genomic and metabolic features that can underlie early successional and opportunistic lifestyles of human gut symbionts Lozupone, Catherine Faust, Karoline Raes, Jeroen Faith, Jeremiah J. Frank, Daniel N. Zaneveld, Jesse Gordon, Jeffrey I. Knight, Rob Genome Res Research We lack a deep understanding of genetic and metabolic attributes specializing in microbial consortia for initial and subsequent waves of colonization of our body habitats. Here we show that phylogenetically interspersed bacteria in Clostridium cluster XIVa, an abundant group of bacteria in the adult human gut also known as the Clostridium coccoides or Eubacterium rectale group, contains species that have evolved distribution patterns consistent with either early successional or stable gut communities. The species that specialize to the infant gut are more likely to associate with systemic infections and can reach high abundances in individuals with Inflammatory Bowel Disease (IBD), indicating that a subset of the microbiota that have adapted to pioneer/opportunistic lifestyles may do well in both early development and with disease. We identified genes likely selected during adaptation to pioneer/opportunistic lifestyles as those for which early succession association and not phylogenetic relationships explain genomic abundance. These genes reveal potential mechanisms by which opportunistic gut bacteria tolerate osmotic and oxidative stress and potentially important aspects of their metabolism. These genes may not only be biomarkers of properties associated with adaptation to early succession and disturbance, but also leads for developing therapies aimed at promoting reestablishment of stable gut communities following physiologic or pathologic disturbances. Cold Spring Harbor Laboratory Press 2012-10 /pmc/articles/PMC3460192/ /pubmed/22665442 http://dx.doi.org/10.1101/gr.138198.112 Text en © 2012, Published by Cold Spring Harbor Laboratory Press This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported License), as described at http://creativecommons.org/licenses/by-nc/3.0/. |
spellingShingle | Research Lozupone, Catherine Faust, Karoline Raes, Jeroen Faith, Jeremiah J. Frank, Daniel N. Zaneveld, Jesse Gordon, Jeffrey I. Knight, Rob Identifying genomic and metabolic features that can underlie early successional and opportunistic lifestyles of human gut symbionts |
title | Identifying genomic and metabolic features that can underlie early successional and opportunistic lifestyles of human gut symbionts |
title_full | Identifying genomic and metabolic features that can underlie early successional and opportunistic lifestyles of human gut symbionts |
title_fullStr | Identifying genomic and metabolic features that can underlie early successional and opportunistic lifestyles of human gut symbionts |
title_full_unstemmed | Identifying genomic and metabolic features that can underlie early successional and opportunistic lifestyles of human gut symbionts |
title_short | Identifying genomic and metabolic features that can underlie early successional and opportunistic lifestyles of human gut symbionts |
title_sort | identifying genomic and metabolic features that can underlie early successional and opportunistic lifestyles of human gut symbionts |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460192/ https://www.ncbi.nlm.nih.gov/pubmed/22665442 http://dx.doi.org/10.1101/gr.138198.112 |
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