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Interplay between the human gut microbiome and host metabolism

The human gut is inhabited by a complex and metabolically active microbial ecosystem. While many studies focused on the effect of individual microbial taxa on human health, their overall metabolic potential has been under-explored. Using whole-metagenome shotgun sequencing data in 1,004 twins, we fi...

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Autores principales: Visconti, Alessia, Le Roy, Caroline I., Rosa, Fabio, Rossi, Niccolò, Martin, Tiphaine C., Mohney, Robert P., Li, Weizhong, de Rinaldis, Emanuele, Bell, Jordana T., Venter, J. Craig, Nelson, Karen E., Spector, Tim D., Falchi, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776654/
https://www.ncbi.nlm.nih.gov/pubmed/31582752
http://dx.doi.org/10.1038/s41467-019-12476-z
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author Visconti, Alessia
Le Roy, Caroline I.
Rosa, Fabio
Rossi, Niccolò
Martin, Tiphaine C.
Mohney, Robert P.
Li, Weizhong
de Rinaldis, Emanuele
Bell, Jordana T.
Venter, J. Craig
Nelson, Karen E.
Spector, Tim D.
Falchi, Mario
author_facet Visconti, Alessia
Le Roy, Caroline I.
Rosa, Fabio
Rossi, Niccolò
Martin, Tiphaine C.
Mohney, Robert P.
Li, Weizhong
de Rinaldis, Emanuele
Bell, Jordana T.
Venter, J. Craig
Nelson, Karen E.
Spector, Tim D.
Falchi, Mario
author_sort Visconti, Alessia
collection PubMed
description The human gut is inhabited by a complex and metabolically active microbial ecosystem. While many studies focused on the effect of individual microbial taxa on human health, their overall metabolic potential has been under-explored. Using whole-metagenome shotgun sequencing data in 1,004 twins, we first observed that unrelated subjects share, on average, almost double the number of metabolic pathways (82%) than species (43%). Then, using 673 blood and 713 faecal metabolites, we found metabolic pathways to be associated with 34% of blood and 95% of faecal metabolites, with over 18,000 significant associations, while species showed less than 3,000 associations. Finally, we estimated that the microbiome was involved in a dialogue between 71% of faecal, and 15% of blood, metabolites. This study underlines the importance of studying the microbial metabolic potential rather than focusing purely on taxonomy to find therapeutic and diagnostic targets, and provides a unique resource describing the interplay between the microbiome and the systemic and faecal metabolic environments.
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spelling pubmed-67766542019-10-07 Interplay between the human gut microbiome and host metabolism Visconti, Alessia Le Roy, Caroline I. Rosa, Fabio Rossi, Niccolò Martin, Tiphaine C. Mohney, Robert P. Li, Weizhong de Rinaldis, Emanuele Bell, Jordana T. Venter, J. Craig Nelson, Karen E. Spector, Tim D. Falchi, Mario Nat Commun Article The human gut is inhabited by a complex and metabolically active microbial ecosystem. While many studies focused on the effect of individual microbial taxa on human health, their overall metabolic potential has been under-explored. Using whole-metagenome shotgun sequencing data in 1,004 twins, we first observed that unrelated subjects share, on average, almost double the number of metabolic pathways (82%) than species (43%). Then, using 673 blood and 713 faecal metabolites, we found metabolic pathways to be associated with 34% of blood and 95% of faecal metabolites, with over 18,000 significant associations, while species showed less than 3,000 associations. Finally, we estimated that the microbiome was involved in a dialogue between 71% of faecal, and 15% of blood, metabolites. This study underlines the importance of studying the microbial metabolic potential rather than focusing purely on taxonomy to find therapeutic and diagnostic targets, and provides a unique resource describing the interplay between the microbiome and the systemic and faecal metabolic environments. Nature Publishing Group UK 2019-10-03 /pmc/articles/PMC6776654/ /pubmed/31582752 http://dx.doi.org/10.1038/s41467-019-12476-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Visconti, Alessia
Le Roy, Caroline I.
Rosa, Fabio
Rossi, Niccolò
Martin, Tiphaine C.
Mohney, Robert P.
Li, Weizhong
de Rinaldis, Emanuele
Bell, Jordana T.
Venter, J. Craig
Nelson, Karen E.
Spector, Tim D.
Falchi, Mario
Interplay between the human gut microbiome and host metabolism
title Interplay between the human gut microbiome and host metabolism
title_full Interplay between the human gut microbiome and host metabolism
title_fullStr Interplay between the human gut microbiome and host metabolism
title_full_unstemmed Interplay between the human gut microbiome and host metabolism
title_short Interplay between the human gut microbiome and host metabolism
title_sort interplay between the human gut microbiome and host metabolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776654/
https://www.ncbi.nlm.nih.gov/pubmed/31582752
http://dx.doi.org/10.1038/s41467-019-12476-z
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