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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...

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Autores principales: Storelli, Gilles, Strigini, Maura, Grenier, Théodore, Bozonnet, Loan, Schwarzer, Martin, Daniel, Catherine, Matos, Renata, Leulier, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2018
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.
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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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