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Association of Fecal Microbial Diversity and Taxonomy with Selected Enzymatic Functions
Few microbial functions have been compared to a comprehensive survey of the human fecal microbiome. We evaluated determinants of fecal microbial β-glucuronidase and β-glucosidase activities, focusing especially on associations with microbial alpha and beta diversity and taxonomy. We enrolled 51 heal...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3386201/ https://www.ncbi.nlm.nih.gov/pubmed/22761886 http://dx.doi.org/10.1371/journal.pone.0039745 |
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author | Flores, Roberto Shi, Jianxin Gail, Mitchell H. Gajer, Pawel Ravel, Jacques Goedert, James J. |
author_facet | Flores, Roberto Shi, Jianxin Gail, Mitchell H. Gajer, Pawel Ravel, Jacques Goedert, James J. |
author_sort | Flores, Roberto |
collection | PubMed |
description | Few microbial functions have been compared to a comprehensive survey of the human fecal microbiome. We evaluated determinants of fecal microbial β-glucuronidase and β-glucosidase activities, focusing especially on associations with microbial alpha and beta diversity and taxonomy. We enrolled 51 healthy volunteers (26 female, mean age 39) who provided questionnaire data and multiple aliquots of a stool, from which proteins were extracted to quantify β-glucuronidase and β-glucosidase activities, and DNA was extracted to amplify and pyrosequence 16S rRNA gene sequences to classify and quantify microbiome diversity and taxonomy. Fecal β-glucuronidase was elevated with weight loss of at least 5 lb. (P = 0.03), whereas β-glucosidase was marginally reduced in the four vegetarians (P = 0.06). Both enzymes were correlated directly with microbiome richness and alpha diversity measures, directly with the abundance of four Firmicutes Clostridia genera, and inversely with the abundance of two other genera (Firmicutes Lactobacillales Streptococcus and Bacteroidetes Rikenellaceae Alistipes) (all P = 0.05–0.0001). Beta diversity reflected the taxonomic associations. These observations suggest that these enzymatic functions are performed by particular taxa and that diversity indices may serve as surrogates of bacterial functions. Independent validation and deeper understanding of these associations are needed, particularly to characterize functions and pathways that may be amenable to manipulation. |
format | Online Article Text |
id | pubmed-3386201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33862012012-07-03 Association of Fecal Microbial Diversity and Taxonomy with Selected Enzymatic Functions Flores, Roberto Shi, Jianxin Gail, Mitchell H. Gajer, Pawel Ravel, Jacques Goedert, James J. PLoS One Research Article Few microbial functions have been compared to a comprehensive survey of the human fecal microbiome. We evaluated determinants of fecal microbial β-glucuronidase and β-glucosidase activities, focusing especially on associations with microbial alpha and beta diversity and taxonomy. We enrolled 51 healthy volunteers (26 female, mean age 39) who provided questionnaire data and multiple aliquots of a stool, from which proteins were extracted to quantify β-glucuronidase and β-glucosidase activities, and DNA was extracted to amplify and pyrosequence 16S rRNA gene sequences to classify and quantify microbiome diversity and taxonomy. Fecal β-glucuronidase was elevated with weight loss of at least 5 lb. (P = 0.03), whereas β-glucosidase was marginally reduced in the four vegetarians (P = 0.06). Both enzymes were correlated directly with microbiome richness and alpha diversity measures, directly with the abundance of four Firmicutes Clostridia genera, and inversely with the abundance of two other genera (Firmicutes Lactobacillales Streptococcus and Bacteroidetes Rikenellaceae Alistipes) (all P = 0.05–0.0001). Beta diversity reflected the taxonomic associations. These observations suggest that these enzymatic functions are performed by particular taxa and that diversity indices may serve as surrogates of bacterial functions. Independent validation and deeper understanding of these associations are needed, particularly to characterize functions and pathways that may be amenable to manipulation. Public Library of Science 2012-06-28 /pmc/articles/PMC3386201/ /pubmed/22761886 http://dx.doi.org/10.1371/journal.pone.0039745 Text en This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Flores, Roberto Shi, Jianxin Gail, Mitchell H. Gajer, Pawel Ravel, Jacques Goedert, James J. Association of Fecal Microbial Diversity and Taxonomy with Selected Enzymatic Functions |
title | Association of Fecal Microbial Diversity and Taxonomy with Selected Enzymatic Functions |
title_full | Association of Fecal Microbial Diversity and Taxonomy with Selected Enzymatic Functions |
title_fullStr | Association of Fecal Microbial Diversity and Taxonomy with Selected Enzymatic Functions |
title_full_unstemmed | Association of Fecal Microbial Diversity and Taxonomy with Selected Enzymatic Functions |
title_short | Association of Fecal Microbial Diversity and Taxonomy with Selected Enzymatic Functions |
title_sort | association of fecal microbial diversity and taxonomy with selected enzymatic functions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3386201/ https://www.ncbi.nlm.nih.gov/pubmed/22761886 http://dx.doi.org/10.1371/journal.pone.0039745 |
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