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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...

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Autores principales: Lozupone, Catherine, Faust, Karoline, Raes, Jeroen, Faith, Jeremiah J., Frank, Daniel N., Zaneveld, Jesse, Gordon, Jeffrey I., Knight, Rob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2012
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.
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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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