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Gut microbes predominantly act as living beneficial partners rather than raw nutrients
Animals and their gut microbes mutually benefit their health. Nutrition plays a central role in this, directly influencing both host and microbial fitness and the nature of their interactions. This makes nutritional symbioses a complex and dynamic tri-system of diet-microbiota-host. Despite recent d...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10366161/ https://www.ncbi.nlm.nih.gov/pubmed/37488173 http://dx.doi.org/10.1038/s41598-023-38669-7 |
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author | da Silva Soares, Nuno Filipe Quagliariello, Andrea Yigitturk, Seren Martino, Maria Elena |
author_facet | da Silva Soares, Nuno Filipe Quagliariello, Andrea Yigitturk, Seren Martino, Maria Elena |
author_sort | da Silva Soares, Nuno Filipe |
collection | PubMed |
description | Animals and their gut microbes mutually benefit their health. Nutrition plays a central role in this, directly influencing both host and microbial fitness and the nature of their interactions. This makes nutritional symbioses a complex and dynamic tri-system of diet-microbiota-host. Despite recent discoveries on this field, full control over the interplay among these partners is challenging and hinders the resolution of fundamental questions, such as how to parse the gut microbes’ effect as raw nutrition or as symbiotic partners? To tackle this, we made use of the well-characterized Drosophila melanogaster/Lactiplantibacillus plantarum experimental model of nutritional symbiosis to generate a quantitative framework of gut microbes’ effect on the host. By coupling experimental assays and Random Forest analysis, we show that the beneficial effect of L. plantarum strains primarily results from the active relationship as symbionts rather than raw nutrients, regardless of the bacterial strain. Metabolomic analysis of both active and inactive bacterial cells further demonstrated the crucial role of the production of beneficial bacterial metabolites, such as N-acetylated-amino-acids, as result of active bacterial growth and function. Altogether, our results provide a ranking and quantification of the main bacterial features contributing to sustain animal growth. We demonstrate that bacterial activity is the predominant and necessary variable involved in bacteria-mediated benefit, followed by strain-specific properties and the nutritional potential of the bacterial cells. This contributes to elucidate the role of beneficial bacteria and probiotics, creating a broad quantitative framework for host-gut microbiome that can be expanded to other model systems. |
format | Online Article Text |
id | pubmed-10366161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103661612023-07-26 Gut microbes predominantly act as living beneficial partners rather than raw nutrients da Silva Soares, Nuno Filipe Quagliariello, Andrea Yigitturk, Seren Martino, Maria Elena Sci Rep Article Animals and their gut microbes mutually benefit their health. Nutrition plays a central role in this, directly influencing both host and microbial fitness and the nature of their interactions. This makes nutritional symbioses a complex and dynamic tri-system of diet-microbiota-host. Despite recent discoveries on this field, full control over the interplay among these partners is challenging and hinders the resolution of fundamental questions, such as how to parse the gut microbes’ effect as raw nutrition or as symbiotic partners? To tackle this, we made use of the well-characterized Drosophila melanogaster/Lactiplantibacillus plantarum experimental model of nutritional symbiosis to generate a quantitative framework of gut microbes’ effect on the host. By coupling experimental assays and Random Forest analysis, we show that the beneficial effect of L. plantarum strains primarily results from the active relationship as symbionts rather than raw nutrients, regardless of the bacterial strain. Metabolomic analysis of both active and inactive bacterial cells further demonstrated the crucial role of the production of beneficial bacterial metabolites, such as N-acetylated-amino-acids, as result of active bacterial growth and function. Altogether, our results provide a ranking and quantification of the main bacterial features contributing to sustain animal growth. We demonstrate that bacterial activity is the predominant and necessary variable involved in bacteria-mediated benefit, followed by strain-specific properties and the nutritional potential of the bacterial cells. This contributes to elucidate the role of beneficial bacteria and probiotics, creating a broad quantitative framework for host-gut microbiome that can be expanded to other model systems. Nature Publishing Group UK 2023-07-24 /pmc/articles/PMC10366161/ /pubmed/37488173 http://dx.doi.org/10.1038/s41598-023-38669-7 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 da Silva Soares, Nuno Filipe Quagliariello, Andrea Yigitturk, Seren Martino, Maria Elena Gut microbes predominantly act as living beneficial partners rather than raw nutrients |
title | Gut microbes predominantly act as living beneficial partners rather than raw nutrients |
title_full | Gut microbes predominantly act as living beneficial partners rather than raw nutrients |
title_fullStr | Gut microbes predominantly act as living beneficial partners rather than raw nutrients |
title_full_unstemmed | Gut microbes predominantly act as living beneficial partners rather than raw nutrients |
title_short | Gut microbes predominantly act as living beneficial partners rather than raw nutrients |
title_sort | gut microbes predominantly act as living beneficial partners rather than raw nutrients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10366161/ https://www.ncbi.nlm.nih.gov/pubmed/37488173 http://dx.doi.org/10.1038/s41598-023-38669-7 |
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