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Intestinal GCN2 controls Drosophila systemic growth in response to Lactiplantibacillus plantarum symbiotic cues encoded by r/tRNA operons

Symbiotic bacteria interact with their host through symbiotic cues. Here, we took advantage of the mutualism between Drosophila and Lactiplantibacillus plantarum (Lp) to investigate a novel mechanism of host-symbiont interaction. Using chemically defined diets, we found that association with Lp impr...

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Autores principales: Grenier, Théodore, Consuegra, Jessika, Ferrarini, Mariana G, Akherraz, Houssam, Bai, Longwei, Dusabyinema, Yves, Rahioui, Isabelle, Da Silva, Pedro, Gillet, Benjamin, Hughes, Sandrine, Ramos, Cathy I, Matos, Renata C, Leulier, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10289812/
https://www.ncbi.nlm.nih.gov/pubmed/37294006
http://dx.doi.org/10.7554/eLife.76584
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author Grenier, Théodore
Consuegra, Jessika
Ferrarini, Mariana G
Akherraz, Houssam
Bai, Longwei
Dusabyinema, Yves
Rahioui, Isabelle
Da Silva, Pedro
Gillet, Benjamin
Hughes, Sandrine
Ramos, Cathy I
Matos, Renata C
Leulier, François
author_facet Grenier, Théodore
Consuegra, Jessika
Ferrarini, Mariana G
Akherraz, Houssam
Bai, Longwei
Dusabyinema, Yves
Rahioui, Isabelle
Da Silva, Pedro
Gillet, Benjamin
Hughes, Sandrine
Ramos, Cathy I
Matos, Renata C
Leulier, François
author_sort Grenier, Théodore
collection PubMed
description Symbiotic bacteria interact with their host through symbiotic cues. Here, we took advantage of the mutualism between Drosophila and Lactiplantibacillus plantarum (Lp) to investigate a novel mechanism of host-symbiont interaction. Using chemically defined diets, we found that association with Lp improves the growth of larvae-fed amino acid-imbalanced diets, even though Lp cannot produce the limiting amino acid. We show that in this context Lp supports its host’s growth through a molecular dialogue that requires functional operons encoding ribosomal and transfer RNAs (r/tRNAs) in Lp and the general control nonderepressible 2 (GCN2) kinase in Drosophila’s enterocytes. Our data indicate that Lp’s r/tRNAs are packaged in extracellular vesicles and activate GCN2 in a subset of larval enterocytes, a mechanism necessary to remodel the intestinal transcriptome and ultimately to support anabolic growth. Based on our findings, we propose a novel beneficial molecular dialogue between host and microbes, which relies on a non-canonical role of GCN2 as a mediator of non-nutritional symbiotic cues encoded by r/tRNA operons.
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spelling pubmed-102898122023-06-24 Intestinal GCN2 controls Drosophila systemic growth in response to Lactiplantibacillus plantarum symbiotic cues encoded by r/tRNA operons Grenier, Théodore Consuegra, Jessika Ferrarini, Mariana G Akherraz, Houssam Bai, Longwei Dusabyinema, Yves Rahioui, Isabelle Da Silva, Pedro Gillet, Benjamin Hughes, Sandrine Ramos, Cathy I Matos, Renata C Leulier, François eLife Developmental Biology Symbiotic bacteria interact with their host through symbiotic cues. Here, we took advantage of the mutualism between Drosophila and Lactiplantibacillus plantarum (Lp) to investigate a novel mechanism of host-symbiont interaction. Using chemically defined diets, we found that association with Lp improves the growth of larvae-fed amino acid-imbalanced diets, even though Lp cannot produce the limiting amino acid. We show that in this context Lp supports its host’s growth through a molecular dialogue that requires functional operons encoding ribosomal and transfer RNAs (r/tRNAs) in Lp and the general control nonderepressible 2 (GCN2) kinase in Drosophila’s enterocytes. Our data indicate that Lp’s r/tRNAs are packaged in extracellular vesicles and activate GCN2 in a subset of larval enterocytes, a mechanism necessary to remodel the intestinal transcriptome and ultimately to support anabolic growth. Based on our findings, we propose a novel beneficial molecular dialogue between host and microbes, which relies on a non-canonical role of GCN2 as a mediator of non-nutritional symbiotic cues encoded by r/tRNA operons. eLife Sciences Publications, Ltd 2023-06-09 /pmc/articles/PMC10289812/ /pubmed/37294006 http://dx.doi.org/10.7554/eLife.76584 Text en © 2023, Grenier et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Grenier, Théodore
Consuegra, Jessika
Ferrarini, Mariana G
Akherraz, Houssam
Bai, Longwei
Dusabyinema, Yves
Rahioui, Isabelle
Da Silva, Pedro
Gillet, Benjamin
Hughes, Sandrine
Ramos, Cathy I
Matos, Renata C
Leulier, François
Intestinal GCN2 controls Drosophila systemic growth in response to Lactiplantibacillus plantarum symbiotic cues encoded by r/tRNA operons
title Intestinal GCN2 controls Drosophila systemic growth in response to Lactiplantibacillus plantarum symbiotic cues encoded by r/tRNA operons
title_full Intestinal GCN2 controls Drosophila systemic growth in response to Lactiplantibacillus plantarum symbiotic cues encoded by r/tRNA operons
title_fullStr Intestinal GCN2 controls Drosophila systemic growth in response to Lactiplantibacillus plantarum symbiotic cues encoded by r/tRNA operons
title_full_unstemmed Intestinal GCN2 controls Drosophila systemic growth in response to Lactiplantibacillus plantarum symbiotic cues encoded by r/tRNA operons
title_short Intestinal GCN2 controls Drosophila systemic growth in response to Lactiplantibacillus plantarum symbiotic cues encoded by r/tRNA operons
title_sort intestinal gcn2 controls drosophila systemic growth in response to lactiplantibacillus plantarum symbiotic cues encoded by r/trna operons
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10289812/
https://www.ncbi.nlm.nih.gov/pubmed/37294006
http://dx.doi.org/10.7554/eLife.76584
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