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Systems-level metabolism of the altered Schaedler flora, a complete gut microbiota

The altered Schaedler flora (ASF) is a model microbial community with both in vivo and in vitro relevance. Here we provide the first characterization of the ASF community in vitro, independent of a murine host. We compared the functional genetic content of the ASF to wild murine metagenomes and foun...

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Autores principales: Biggs, Matthew B, Medlock, Gregory L, Moutinho, Thomas J, Lees, Hannah J, Swann, Jonathan R, Kolling, Glynis L, Papin, Jason A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5270571/
https://www.ncbi.nlm.nih.gov/pubmed/27824342
http://dx.doi.org/10.1038/ismej.2016.130
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author Biggs, Matthew B
Medlock, Gregory L
Moutinho, Thomas J
Lees, Hannah J
Swann, Jonathan R
Kolling, Glynis L
Papin, Jason A
author_facet Biggs, Matthew B
Medlock, Gregory L
Moutinho, Thomas J
Lees, Hannah J
Swann, Jonathan R
Kolling, Glynis L
Papin, Jason A
author_sort Biggs, Matthew B
collection PubMed
description The altered Schaedler flora (ASF) is a model microbial community with both in vivo and in vitro relevance. Here we provide the first characterization of the ASF community in vitro, independent of a murine host. We compared the functional genetic content of the ASF to wild murine metagenomes and found that the ASF functionally represents wild microbiomes better than random consortia of similar taxonomic composition. We developed a chemically defined medium that supported growth of seven of the eight ASF members. To elucidate the metabolic capabilities of these ASF species—including potential for interactions such as cross-feeding—we performed a spent media screen and analyzed the results through dynamic growth measurements and non-targeted metabolic profiling. We found that cross-feeding is relatively rare (32 of 3570 possible cases), but is enriched between Clostridium ASF356 and Parabacteroides ASF519. We identified many cases of emergent metabolism (856 of 3570 possible cases). These data will inform efforts to understand ASF dynamics and spatial distribution in vivo, to design pre- and probiotics that modulate relative abundances of ASF members, and will be essential for validating computational models of ASF metabolism. Well-characterized, experimentally tractable microbial communities enable research that can translate into more effective microbiome-targeted therapies to improve human health.
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spelling pubmed-52705712017-02-07 Systems-level metabolism of the altered Schaedler flora, a complete gut microbiota Biggs, Matthew B Medlock, Gregory L Moutinho, Thomas J Lees, Hannah J Swann, Jonathan R Kolling, Glynis L Papin, Jason A ISME J Original Article The altered Schaedler flora (ASF) is a model microbial community with both in vivo and in vitro relevance. Here we provide the first characterization of the ASF community in vitro, independent of a murine host. We compared the functional genetic content of the ASF to wild murine metagenomes and found that the ASF functionally represents wild microbiomes better than random consortia of similar taxonomic composition. We developed a chemically defined medium that supported growth of seven of the eight ASF members. To elucidate the metabolic capabilities of these ASF species—including potential for interactions such as cross-feeding—we performed a spent media screen and analyzed the results through dynamic growth measurements and non-targeted metabolic profiling. We found that cross-feeding is relatively rare (32 of 3570 possible cases), but is enriched between Clostridium ASF356 and Parabacteroides ASF519. We identified many cases of emergent metabolism (856 of 3570 possible cases). These data will inform efforts to understand ASF dynamics and spatial distribution in vivo, to design pre- and probiotics that modulate relative abundances of ASF members, and will be essential for validating computational models of ASF metabolism. Well-characterized, experimentally tractable microbial communities enable research that can translate into more effective microbiome-targeted therapies to improve human health. Nature Publishing Group 2017-02 2016-11-08 /pmc/articles/PMC5270571/ /pubmed/27824342 http://dx.doi.org/10.1038/ismej.2016.130 Text en Copyright © 2017 International Society for Microbial Ecology http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Biggs, Matthew B
Medlock, Gregory L
Moutinho, Thomas J
Lees, Hannah J
Swann, Jonathan R
Kolling, Glynis L
Papin, Jason A
Systems-level metabolism of the altered Schaedler flora, a complete gut microbiota
title Systems-level metabolism of the altered Schaedler flora, a complete gut microbiota
title_full Systems-level metabolism of the altered Schaedler flora, a complete gut microbiota
title_fullStr Systems-level metabolism of the altered Schaedler flora, a complete gut microbiota
title_full_unstemmed Systems-level metabolism of the altered Schaedler flora, a complete gut microbiota
title_short Systems-level metabolism of the altered Schaedler flora, a complete gut microbiota
title_sort systems-level metabolism of the altered schaedler flora, a complete gut microbiota
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5270571/
https://www.ncbi.nlm.nih.gov/pubmed/27824342
http://dx.doi.org/10.1038/ismej.2016.130
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