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Untargeted Gut Metabolomics to Delve the Interplay between Selenium Supplementation and Gut Microbiota
[Image: see text] Selenium (Se) is an essential trace element with important health roles due to the antioxidant properties of selenoproteins. To analyze the interplay between Se and gut microbiota, gut metabolomic profiles were determined in conventional (C) and microbiota depleted mice (Abx) after...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8902802/ https://www.ncbi.nlm.nih.gov/pubmed/34734730 http://dx.doi.org/10.1021/acs.jproteome.1c00411 |
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author | Callejón-Leblic, Belén Selma-Royo, Marta Collado, María Carmen Gómez-Ariza, José Luis Abril, Nieves García-Barrera, Tamara |
author_facet | Callejón-Leblic, Belén Selma-Royo, Marta Collado, María Carmen Gómez-Ariza, José Luis Abril, Nieves García-Barrera, Tamara |
author_sort | Callejón-Leblic, Belén |
collection | PubMed |
description | [Image: see text] Selenium (Se) is an essential trace element with important health roles due to the antioxidant properties of selenoproteins. To analyze the interplay between Se and gut microbiota, gut metabolomic profiles were determined in conventional (C) and microbiota depleted mice (Abx) after Se-supplementation (Abx-Se) by untargeted metabolomics, using an analytical multiplatform based on GC-MS and UHPLC-QTOF-MS (MassIVE ID MSV000087829). Gut microbiota profiling was performed by 16S rRNA gene amplicon sequencing. Significant differences in the levels of about 70% of the gut metabolites determined, including fatty acyls, glycerolipids, glycerophospholipids, and steroids, were found in Abx-Se compared to Abx, and only 30% were different between Abx-Se and C, suggesting an important effect of Se-supplementation on Abx mice metabolism. At genus level, the correlation analysis showed strong associations between metabolites and gut bacterial profiles. Likewise, higher abundance of Lactobacillus spp., a potentially beneficial genus enriched after Se-supplementation, was associated with higher levels of prenol lipids, phosphatidylglycerols (C-Se), steroids and diterpenoids (Abx-Se), and also with lower levels of fatty acids (Abx-Se). Thus, we observed a crucial interaction between Se intake–microbiota–metabolites, although further studies to clarify the specific mechanisms are needed. This is the first study about untargeted gut metabolomics after microbiota depletion and Se-supplementation. |
format | Online Article Text |
id | pubmed-8902802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-89028022022-03-09 Untargeted Gut Metabolomics to Delve the Interplay between Selenium Supplementation and Gut Microbiota Callejón-Leblic, Belén Selma-Royo, Marta Collado, María Carmen Gómez-Ariza, José Luis Abril, Nieves García-Barrera, Tamara J Proteome Res [Image: see text] Selenium (Se) is an essential trace element with important health roles due to the antioxidant properties of selenoproteins. To analyze the interplay between Se and gut microbiota, gut metabolomic profiles were determined in conventional (C) and microbiota depleted mice (Abx) after Se-supplementation (Abx-Se) by untargeted metabolomics, using an analytical multiplatform based on GC-MS and UHPLC-QTOF-MS (MassIVE ID MSV000087829). Gut microbiota profiling was performed by 16S rRNA gene amplicon sequencing. Significant differences in the levels of about 70% of the gut metabolites determined, including fatty acyls, glycerolipids, glycerophospholipids, and steroids, were found in Abx-Se compared to Abx, and only 30% were different between Abx-Se and C, suggesting an important effect of Se-supplementation on Abx mice metabolism. At genus level, the correlation analysis showed strong associations between metabolites and gut bacterial profiles. Likewise, higher abundance of Lactobacillus spp., a potentially beneficial genus enriched after Se-supplementation, was associated with higher levels of prenol lipids, phosphatidylglycerols (C-Se), steroids and diterpenoids (Abx-Se), and also with lower levels of fatty acids (Abx-Se). Thus, we observed a crucial interaction between Se intake–microbiota–metabolites, although further studies to clarify the specific mechanisms are needed. This is the first study about untargeted gut metabolomics after microbiota depletion and Se-supplementation. American Chemical Society 2021-11-04 2022-03-04 /pmc/articles/PMC8902802/ /pubmed/34734730 http://dx.doi.org/10.1021/acs.jproteome.1c00411 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Callejón-Leblic, Belén Selma-Royo, Marta Collado, María Carmen Gómez-Ariza, José Luis Abril, Nieves García-Barrera, Tamara Untargeted Gut Metabolomics to Delve the Interplay between Selenium Supplementation and Gut Microbiota |
title | Untargeted Gut
Metabolomics to Delve the Interplay
between Selenium Supplementation and Gut Microbiota |
title_full | Untargeted Gut
Metabolomics to Delve the Interplay
between Selenium Supplementation and Gut Microbiota |
title_fullStr | Untargeted Gut
Metabolomics to Delve the Interplay
between Selenium Supplementation and Gut Microbiota |
title_full_unstemmed | Untargeted Gut
Metabolomics to Delve the Interplay
between Selenium Supplementation and Gut Microbiota |
title_short | Untargeted Gut
Metabolomics to Delve the Interplay
between Selenium Supplementation and Gut Microbiota |
title_sort | untargeted gut
metabolomics to delve the interplay
between selenium supplementation and gut microbiota |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8902802/ https://www.ncbi.nlm.nih.gov/pubmed/34734730 http://dx.doi.org/10.1021/acs.jproteome.1c00411 |
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