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The human microbial exposome: expanding the Exposome-Explorer database with gut microbial metabolites

Metabolites produced by the gut microbiota play an important role in the cross-talk with the human host. Many microbial metabolites are biologically active and can pass the gut barrier and make it into the systemic circulation, where they form the gut microbial exposome, i.e. the totality of gut mic...

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Autores principales: Neveu, Vanessa, Nicolas, Geneviève, Amara, Adam, Salek, Reza M., Scalbert, Augustin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9894932/
https://www.ncbi.nlm.nih.gov/pubmed/36732606
http://dx.doi.org/10.1038/s41598-022-26366-w
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author Neveu, Vanessa
Nicolas, Geneviève
Amara, Adam
Salek, Reza M.
Scalbert, Augustin
author_facet Neveu, Vanessa
Nicolas, Geneviève
Amara, Adam
Salek, Reza M.
Scalbert, Augustin
author_sort Neveu, Vanessa
collection PubMed
description Metabolites produced by the gut microbiota play an important role in the cross-talk with the human host. Many microbial metabolites are biologically active and can pass the gut barrier and make it into the systemic circulation, where they form the gut microbial exposome, i.e. the totality of gut microbial metabolites in body fluids or tissues of the host. A major difficulty faced when studying the microbial exposome and its role in health and diseases is to differentiate metabolites solely or partially derived from microbial metabolism from those produced by the host or coming from the diet. Our objective was to collect data from the scientific literature and build a database on gut microbial metabolites and on evidence of their microbial origin. Three types of evidence on the microbial origin of the gut microbial exposome were defined: (1) metabolites are produced in vitro by human faecal bacteria; (2) metabolites show reduced concentrations in humans or experimental animals upon treatment with antibiotics; (3) metabolites show reduced concentrations in germ-free animals when compared with conventional animals. Data was manually collected from peer-reviewed publications and inserted in the Exposome-Explorer database. Furthermore, to explore the chemical space of the microbial exposome and predict metabolites uniquely formed by the microbiota, genome-scale metabolic models (GSMMs) of gut bacterial strains and humans were compared. A total of 1848 records on one or more types of evidence on the gut microbial origin of 457 metabolites was collected in Exposome-Explorer. Data on their known precursors and concentrations in human blood, urine and faeces was also collected. About 66% of the predicted gut microbial metabolites (n = 1543) were found to be unique microbial metabolites not found in the human GSMM, neither in the list of 457 metabolites curated in Exposome-Explorer, and can be targets for new experimental studies. This new data on the gut microbial exposome, freely available in Exposome-Explorer (http://exposome-explorer.iarc.fr/), will help researchers to identify poorly studied microbial metabolites to be considered in future studies on the gut microbiota, and study their functionalities and role in health and diseases.
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spelling pubmed-98949322023-02-04 The human microbial exposome: expanding the Exposome-Explorer database with gut microbial metabolites Neveu, Vanessa Nicolas, Geneviève Amara, Adam Salek, Reza M. Scalbert, Augustin Sci Rep Article Metabolites produced by the gut microbiota play an important role in the cross-talk with the human host. Many microbial metabolites are biologically active and can pass the gut barrier and make it into the systemic circulation, where they form the gut microbial exposome, i.e. the totality of gut microbial metabolites in body fluids or tissues of the host. A major difficulty faced when studying the microbial exposome and its role in health and diseases is to differentiate metabolites solely or partially derived from microbial metabolism from those produced by the host or coming from the diet. Our objective was to collect data from the scientific literature and build a database on gut microbial metabolites and on evidence of their microbial origin. Three types of evidence on the microbial origin of the gut microbial exposome were defined: (1) metabolites are produced in vitro by human faecal bacteria; (2) metabolites show reduced concentrations in humans or experimental animals upon treatment with antibiotics; (3) metabolites show reduced concentrations in germ-free animals when compared with conventional animals. Data was manually collected from peer-reviewed publications and inserted in the Exposome-Explorer database. Furthermore, to explore the chemical space of the microbial exposome and predict metabolites uniquely formed by the microbiota, genome-scale metabolic models (GSMMs) of gut bacterial strains and humans were compared. A total of 1848 records on one or more types of evidence on the gut microbial origin of 457 metabolites was collected in Exposome-Explorer. Data on their known precursors and concentrations in human blood, urine and faeces was also collected. About 66% of the predicted gut microbial metabolites (n = 1543) were found to be unique microbial metabolites not found in the human GSMM, neither in the list of 457 metabolites curated in Exposome-Explorer, and can be targets for new experimental studies. This new data on the gut microbial exposome, freely available in Exposome-Explorer (http://exposome-explorer.iarc.fr/), will help researchers to identify poorly studied microbial metabolites to be considered in future studies on the gut microbiota, and study their functionalities and role in health and diseases. Nature Publishing Group UK 2023-02-02 /pmc/articles/PMC9894932/ /pubmed/36732606 http://dx.doi.org/10.1038/s41598-022-26366-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Neveu, Vanessa
Nicolas, Geneviève
Amara, Adam
Salek, Reza M.
Scalbert, Augustin
The human microbial exposome: expanding the Exposome-Explorer database with gut microbial metabolites
title The human microbial exposome: expanding the Exposome-Explorer database with gut microbial metabolites
title_full The human microbial exposome: expanding the Exposome-Explorer database with gut microbial metabolites
title_fullStr The human microbial exposome: expanding the Exposome-Explorer database with gut microbial metabolites
title_full_unstemmed The human microbial exposome: expanding the Exposome-Explorer database with gut microbial metabolites
title_short The human microbial exposome: expanding the Exposome-Explorer database with gut microbial metabolites
title_sort human microbial exposome: expanding the exposome-explorer database with gut microbial metabolites
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9894932/
https://www.ncbi.nlm.nih.gov/pubmed/36732606
http://dx.doi.org/10.1038/s41598-022-26366-w
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