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Modeling Drosophila gut microbe interactions reveals metabolic interconnectivity

We know a lot about varying gut microbiome compositions. Yet, how the bacteria affect each other remains elusive. In mammals, this is largely based on the sheer complexity of the microbiome with at least hundreds of different species. Thus, model organisms such as Drosophila melanogaster are commonl...

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Autores principales: Schönborn, Jürgen W., Stewart, Fiona A., Enriquez, Kerstin Maas, Akhtar, Irfan, Droste, Andrea, Waschina, Silvio, Beller, Mathias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528732/
https://www.ncbi.nlm.nih.gov/pubmed/34712918
http://dx.doi.org/10.1016/j.isci.2021.103216
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author Schönborn, Jürgen W.
Stewart, Fiona A.
Enriquez, Kerstin Maas
Akhtar, Irfan
Droste, Andrea
Waschina, Silvio
Beller, Mathias
author_facet Schönborn, Jürgen W.
Stewart, Fiona A.
Enriquez, Kerstin Maas
Akhtar, Irfan
Droste, Andrea
Waschina, Silvio
Beller, Mathias
author_sort Schönborn, Jürgen W.
collection PubMed
description We know a lot about varying gut microbiome compositions. Yet, how the bacteria affect each other remains elusive. In mammals, this is largely based on the sheer complexity of the microbiome with at least hundreds of different species. Thus, model organisms such as Drosophila melanogaster are commonly used to investigate mechanistic questions as the microbiome consists of only about 10 leading bacterial species. Here, we isolated gut bacteria from laboratory-reared Drosophila, sequenced their respective genomes, and used this information to reconstruct genome-scale metabolic models. With these, we simulated growth in mono- and co-culture conditions and different media including a synthetic diet designed to grow Drosophila melanogaster. Our simulations reveal a synergistic growth of some but not all gut microbiome members, which stems on the exchange of distinct metabolites including tricarboxylic acid cycle intermediates. Culturing experiments confirmed our predictions. Our study thus demonstrates the possibility to predict microbiome-derived growth-promoting cross-feeding.
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spelling pubmed-85287322021-10-27 Modeling Drosophila gut microbe interactions reveals metabolic interconnectivity Schönborn, Jürgen W. Stewart, Fiona A. Enriquez, Kerstin Maas Akhtar, Irfan Droste, Andrea Waschina, Silvio Beller, Mathias iScience Article We know a lot about varying gut microbiome compositions. Yet, how the bacteria affect each other remains elusive. In mammals, this is largely based on the sheer complexity of the microbiome with at least hundreds of different species. Thus, model organisms such as Drosophila melanogaster are commonly used to investigate mechanistic questions as the microbiome consists of only about 10 leading bacterial species. Here, we isolated gut bacteria from laboratory-reared Drosophila, sequenced their respective genomes, and used this information to reconstruct genome-scale metabolic models. With these, we simulated growth in mono- and co-culture conditions and different media including a synthetic diet designed to grow Drosophila melanogaster. Our simulations reveal a synergistic growth of some but not all gut microbiome members, which stems on the exchange of distinct metabolites including tricarboxylic acid cycle intermediates. Culturing experiments confirmed our predictions. Our study thus demonstrates the possibility to predict microbiome-derived growth-promoting cross-feeding. Elsevier 2021-10-06 /pmc/articles/PMC8528732/ /pubmed/34712918 http://dx.doi.org/10.1016/j.isci.2021.103216 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Schönborn, Jürgen W.
Stewart, Fiona A.
Enriquez, Kerstin Maas
Akhtar, Irfan
Droste, Andrea
Waschina, Silvio
Beller, Mathias
Modeling Drosophila gut microbe interactions reveals metabolic interconnectivity
title Modeling Drosophila gut microbe interactions reveals metabolic interconnectivity
title_full Modeling Drosophila gut microbe interactions reveals metabolic interconnectivity
title_fullStr Modeling Drosophila gut microbe interactions reveals metabolic interconnectivity
title_full_unstemmed Modeling Drosophila gut microbe interactions reveals metabolic interconnectivity
title_short Modeling Drosophila gut microbe interactions reveals metabolic interconnectivity
title_sort modeling drosophila gut microbe interactions reveals metabolic interconnectivity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528732/
https://www.ncbi.nlm.nih.gov/pubmed/34712918
http://dx.doi.org/10.1016/j.isci.2021.103216
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