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...
Main Authors: | , , , , , , , , , , |
---|---|
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 |
id |
doaj-3b2c6068fa2f4295bef35ec91d23410a |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT jessikaconsuegra drosophilaassociatedbacteriadifferentiallyshapethenutritionalrequirementsoftheirhostduringjuvenilegrowth AT theodoregrenier drosophilaassociatedbacteriadifferentiallyshapethenutritionalrequirementsoftheirhostduringjuvenilegrowth AT patricebaapuyoulet drosophilaassociatedbacteriadifferentiallyshapethenutritionalrequirementsoftheirhostduringjuvenilegrowth AT isabellerahioui drosophilaassociatedbacteriadifferentiallyshapethenutritionalrequirementsoftheirhostduringjuvenilegrowth AT houssamakherraz drosophilaassociatedbacteriadifferentiallyshapethenutritionalrequirementsoftheirhostduringjuvenilegrowth AT hugogervais drosophilaassociatedbacteriadifferentiallyshapethenutritionalrequirementsoftheirhostduringjuvenilegrowth AT nicolasparisot drosophilaassociatedbacteriadifferentiallyshapethenutritionalrequirementsoftheirhostduringjuvenilegrowth AT pedrodasilva drosophilaassociatedbacteriadifferentiallyshapethenutritionalrequirementsoftheirhostduringjuvenilegrowth AT hubertcharles drosophilaassociatedbacteriadifferentiallyshapethenutritionalrequirementsoftheirhostduringjuvenilegrowth AT federicacalevro drosophilaassociatedbacteriadifferentiallyshapethenutritionalrequirementsoftheirhostduringjuvenilegrowth AT francoisleulier drosophilaassociatedbacteriadifferentiallyshapethenutritionalrequirementsoftheirhostduringjuvenilegrowth |
_version_ |
1721322039088775168 |