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Drosophila Perpetuates Nutritional Mutualism by Promoting the Fitness of Its Intestinal Symbiont Lactobacillus plantarum
Facultative animal-bacteria symbioses, which are critical determinants of animal fitness, are largely assumed to be mutualistic. However, whether commensal bacteria benefit from the association has not been rigorously assessed. Using a simple and tractable gnotobiotic model— Drosophila mono-associat...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5807057/ https://www.ncbi.nlm.nih.gov/pubmed/29290388 http://dx.doi.org/10.1016/j.cmet.2017.11.011 |
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author | Storelli, Gilles Strigini, Maura Grenier, Théodore Bozonnet, Loan Schwarzer, Martin Daniel, Catherine Matos, Renata Leulier, François |
author_facet | Storelli, Gilles Strigini, Maura Grenier, Théodore Bozonnet, Loan Schwarzer, Martin Daniel, Catherine Matos, Renata Leulier, François |
author_sort | Storelli, Gilles |
collection | PubMed |
description | Facultative animal-bacteria symbioses, which are critical determinants of animal fitness, are largely assumed to be mutualistic. However, whether commensal bacteria benefit from the association has not been rigorously assessed. Using a simple and tractable gnotobiotic model— Drosophila mono-associated with one of its dominant commensals, Lactobacillus plantarum—we reveal that in addition to benefiting animal growth, this facultative symbiosis has a positive impact on commensal bacteria fitness. We find that bacteria encounter a strong cost during gut transit, yet larvae-derived maintenance factors override this cost and increase bacterial population fitness, thus perpetuating symbiosis. In addition, we demonstrate that the maintenance of the association is required for achieving maximum animal growth benefits upon chronic undernutrition. Taken together, our study establishes a prototypical case of facultative nutritional mutualism, whereby a farming mechanism perpetuates animal-bacteria symbiosis, which bolsters fitness gains for both partners upon poor nutritional conditions. |
format | Online Article Text |
id | pubmed-5807057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58070572018-02-13 Drosophila Perpetuates Nutritional Mutualism by Promoting the Fitness of Its Intestinal Symbiont Lactobacillus plantarum Storelli, Gilles Strigini, Maura Grenier, Théodore Bozonnet, Loan Schwarzer, Martin Daniel, Catherine Matos, Renata Leulier, François Cell Metab Article Facultative animal-bacteria symbioses, which are critical determinants of animal fitness, are largely assumed to be mutualistic. However, whether commensal bacteria benefit from the association has not been rigorously assessed. Using a simple and tractable gnotobiotic model— Drosophila mono-associated with one of its dominant commensals, Lactobacillus plantarum—we reveal that in addition to benefiting animal growth, this facultative symbiosis has a positive impact on commensal bacteria fitness. We find that bacteria encounter a strong cost during gut transit, yet larvae-derived maintenance factors override this cost and increase bacterial population fitness, thus perpetuating symbiosis. In addition, we demonstrate that the maintenance of the association is required for achieving maximum animal growth benefits upon chronic undernutrition. Taken together, our study establishes a prototypical case of facultative nutritional mutualism, whereby a farming mechanism perpetuates animal-bacteria symbiosis, which bolsters fitness gains for both partners upon poor nutritional conditions. Cell Press 2018-02-06 /pmc/articles/PMC5807057/ /pubmed/29290388 http://dx.doi.org/10.1016/j.cmet.2017.11.011 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Storelli, Gilles Strigini, Maura Grenier, Théodore Bozonnet, Loan Schwarzer, Martin Daniel, Catherine Matos, Renata Leulier, François Drosophila Perpetuates Nutritional Mutualism by Promoting the Fitness of Its Intestinal Symbiont Lactobacillus plantarum |
title | Drosophila Perpetuates Nutritional Mutualism by Promoting the Fitness of Its Intestinal Symbiont Lactobacillus plantarum |
title_full | Drosophila Perpetuates Nutritional Mutualism by Promoting the Fitness of Its Intestinal Symbiont Lactobacillus plantarum |
title_fullStr | Drosophila Perpetuates Nutritional Mutualism by Promoting the Fitness of Its Intestinal Symbiont Lactobacillus plantarum |
title_full_unstemmed | Drosophila Perpetuates Nutritional Mutualism by Promoting the Fitness of Its Intestinal Symbiont Lactobacillus plantarum |
title_short | Drosophila Perpetuates Nutritional Mutualism by Promoting the Fitness of Its Intestinal Symbiont Lactobacillus plantarum |
title_sort | drosophila perpetuates nutritional mutualism by promoting the fitness of its intestinal symbiont lactobacillus plantarum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5807057/ https://www.ncbi.nlm.nih.gov/pubmed/29290388 http://dx.doi.org/10.1016/j.cmet.2017.11.011 |
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