Drosophila-associated bacteria differentially shape the nutritional requirements of their host during juvenile growth.

The interplay between nutrition and the microbial communities colonizing the gastrointestinal tract (i.e., gut microbiota) determines juvenile growth trajectory. Nutritional deficiencies trigger developmental delays, and an immature gut microbiota is a hallmark of pathologies related to childhood un...

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Main Authors: Jessika Consuegra, Théodore Grenier, Patrice Baa-Puyoulet, Isabelle Rahioui, Houssam Akherraz, Hugo Gervais, Nicolas Parisot, Pedro da Silva, Hubert Charles, Federica Calevro, François Leulier
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-03-01
Series:PLoS Biology
Online Access:https://doi.org/10.1371/journal.pbio.3000681
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spelling doaj-3b2c6068fa2f4295bef35ec91d23410a2021-07-02T21:21:59ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852020-03-01183e300068110.1371/journal.pbio.3000681Drosophila-associated bacteria differentially shape the nutritional requirements of their host during juvenile growth.Jessika ConsuegraThéodore GrenierPatrice Baa-PuyouletIsabelle RahiouiHoussam AkherrazHugo GervaisNicolas ParisotPedro da SilvaHubert CharlesFederica CalevroFrançois LeulierThe interplay between nutrition and the microbial communities colonizing the gastrointestinal tract (i.e., gut microbiota) determines juvenile growth trajectory. Nutritional deficiencies trigger developmental delays, and an immature gut microbiota is a hallmark of pathologies related to childhood undernutrition. However, how host-associated bacteria modulate the impact of nutrition on juvenile growth remains elusive. Here, using gnotobiotic Drosophila melanogaster larvae independently associated with Acetobacter pomorumWJL (ApWJL) and Lactobacillus plantarumNC8 (LpNC8), 2 model Drosophila-associated bacteria, we performed a large-scale, systematic nutritional screen based on larval growth in 40 different and precisely controlled nutritional environments. We combined these results with genome-based metabolic network reconstruction to define the biosynthetic capacities of Drosophila germ-free (GF) larvae and its 2 bacterial partners. We first established that ApWJL and LpNC8 differentially fulfill the nutritional requirements of the ex-GF larvae and parsed such difference down to individual amino acids, vitamins, other micronutrients, and trace metals. We found that Drosophila-associated bacteria not only fortify the host's diet with essential nutrients but, in specific instances, functionally compensate for host auxotrophies by either providing a metabolic intermediate or nutrient derivative to the host or by uptaking, concentrating, and delivering contaminant traces of micronutrients. Our systematic work reveals that beyond the molecular dialogue engaged between the host and its bacterial partners, Drosophila and its associated bacteria establish an integrated nutritional network relying on nutrient provision and utilization.https://doi.org/10.1371/journal.pbio.3000681
collection DOAJ
language English
format Article
sources DOAJ
author Jessika Consuegra
Théodore Grenier
Patrice Baa-Puyoulet
Isabelle Rahioui
Houssam Akherraz
Hugo Gervais
Nicolas Parisot
Pedro da Silva
Hubert Charles
Federica Calevro
François Leulier
spellingShingle Jessika Consuegra
Théodore Grenier
Patrice Baa-Puyoulet
Isabelle Rahioui
Houssam Akherraz
Hugo Gervais
Nicolas Parisot
Pedro da Silva
Hubert Charles
Federica Calevro
François Leulier
Drosophila-associated bacteria differentially shape the nutritional requirements of their host during juvenile growth.
PLoS Biology
author_facet Jessika Consuegra
Théodore Grenier
Patrice Baa-Puyoulet
Isabelle Rahioui
Houssam Akherraz
Hugo Gervais
Nicolas Parisot
Pedro da Silva
Hubert Charles
Federica Calevro
François Leulier
author_sort Jessika Consuegra
title Drosophila-associated bacteria differentially shape the nutritional requirements of their host during juvenile growth.
title_short Drosophila-associated bacteria differentially shape the nutritional requirements of their host during juvenile growth.
title_full Drosophila-associated bacteria differentially shape the nutritional requirements of their host during juvenile growth.
title_fullStr Drosophila-associated bacteria differentially shape the nutritional requirements of their host during juvenile growth.
title_full_unstemmed Drosophila-associated bacteria differentially shape the nutritional requirements of their host during juvenile growth.
title_sort drosophila-associated bacteria differentially shape the nutritional requirements of their host during juvenile growth.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2020-03-01
description The interplay between nutrition and the microbial communities colonizing the gastrointestinal tract (i.e., gut microbiota) determines juvenile growth trajectory. Nutritional deficiencies trigger developmental delays, and an immature gut microbiota is a hallmark of pathologies related to childhood undernutrition. However, how host-associated bacteria modulate the impact of nutrition on juvenile growth remains elusive. Here, using gnotobiotic Drosophila melanogaster larvae independently associated with Acetobacter pomorumWJL (ApWJL) and Lactobacillus plantarumNC8 (LpNC8), 2 model Drosophila-associated bacteria, we performed a large-scale, systematic nutritional screen based on larval growth in 40 different and precisely controlled nutritional environments. We combined these results with genome-based metabolic network reconstruction to define the biosynthetic capacities of Drosophila germ-free (GF) larvae and its 2 bacterial partners. We first established that ApWJL and LpNC8 differentially fulfill the nutritional requirements of the ex-GF larvae and parsed such difference down to individual amino acids, vitamins, other micronutrients, and trace metals. We found that Drosophila-associated bacteria not only fortify the host's diet with essential nutrients but, in specific instances, functionally compensate for host auxotrophies by either providing a metabolic intermediate or nutrient derivative to the host or by uptaking, concentrating, and delivering contaminant traces of micronutrients. Our systematic work reveals that beyond the molecular dialogue engaged between the host and its bacterial partners, Drosophila and its associated bacteria establish an integrated nutritional network relying on nutrient provision and utilization.
url https://doi.org/10.1371/journal.pbio.3000681
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