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Microbiome derived acidity protects against microbial invasion in Drosophila

Microbial invasions underlie host-microbe interactions that result in microbial pathogenesis and probiotic colonization. While these processes are of broad interest, there are still gaps in our understanding of the barriers to entry and how some microbes overcome them. In this study, we explore the...

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Autores principales: Barron, Alexander J., Lesperance, Danielle N. A., Doucette, Jeremy, Calle, Sthefany, Broderick, Nichole A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9882140/
https://www.ncbi.nlm.nih.gov/pubmed/36711873
http://dx.doi.org/10.1101/2023.01.12.523836
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author Barron, Alexander J.
Lesperance, Danielle N. A.
Doucette, Jeremy
Calle, Sthefany
Broderick, Nichole A.
author_facet Barron, Alexander J.
Lesperance, Danielle N. A.
Doucette, Jeremy
Calle, Sthefany
Broderick, Nichole A.
author_sort Barron, Alexander J.
collection PubMed
description Microbial invasions underlie host-microbe interactions that result in microbial pathogenesis and probiotic colonization. While these processes are of broad interest, there are still gaps in our understanding of the barriers to entry and how some microbes overcome them. In this study, we explore the effects of the microbiome on invasions of foreign microbes in Drosophila melanogaster. We demonstrate that gut microbes Lactiplantibacillus plantarum and Acetobacter tropicalis improve survival during invasion of a lethal gut pathogen and lead to a reduction in microbial burden. Using a novel multi-organism interactions assay, we report that L. plantarum inhibits the growth of three invasive Gram-negative bacteria, while A. tropicalis prevents this inhibition. A series of in vitro and in vivo experiments revealed that inhibition by L. plantarum is linked to its ability to acidify both internal and external environments, including culture media, fly food, and the gut itself, while A. tropicalis diminishes the inhibition by quenching acids. We propose that acid produced by the microbiome serves as an important gatekeeper to microbial invasions, as only microbes capable of tolerating acidic environments can colonize the host. The methods described herein will add to the growing breadth of tools to study microbe-microbe interactions in broad contexts.
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spelling pubmed-98821402023-01-28 Microbiome derived acidity protects against microbial invasion in Drosophila Barron, Alexander J. Lesperance, Danielle N. A. Doucette, Jeremy Calle, Sthefany Broderick, Nichole A. bioRxiv Article Microbial invasions underlie host-microbe interactions that result in microbial pathogenesis and probiotic colonization. While these processes are of broad interest, there are still gaps in our understanding of the barriers to entry and how some microbes overcome them. In this study, we explore the effects of the microbiome on invasions of foreign microbes in Drosophila melanogaster. We demonstrate that gut microbes Lactiplantibacillus plantarum and Acetobacter tropicalis improve survival during invasion of a lethal gut pathogen and lead to a reduction in microbial burden. Using a novel multi-organism interactions assay, we report that L. plantarum inhibits the growth of three invasive Gram-negative bacteria, while A. tropicalis prevents this inhibition. A series of in vitro and in vivo experiments revealed that inhibition by L. plantarum is linked to its ability to acidify both internal and external environments, including culture media, fly food, and the gut itself, while A. tropicalis diminishes the inhibition by quenching acids. We propose that acid produced by the microbiome serves as an important gatekeeper to microbial invasions, as only microbes capable of tolerating acidic environments can colonize the host. The methods described herein will add to the growing breadth of tools to study microbe-microbe interactions in broad contexts. Cold Spring Harbor Laboratory 2023-01-12 /pmc/articles/PMC9882140/ /pubmed/36711873 http://dx.doi.org/10.1101/2023.01.12.523836 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Barron, Alexander J.
Lesperance, Danielle N. A.
Doucette, Jeremy
Calle, Sthefany
Broderick, Nichole A.
Microbiome derived acidity protects against microbial invasion in Drosophila
title Microbiome derived acidity protects against microbial invasion in Drosophila
title_full Microbiome derived acidity protects against microbial invasion in Drosophila
title_fullStr Microbiome derived acidity protects against microbial invasion in Drosophila
title_full_unstemmed Microbiome derived acidity protects against microbial invasion in Drosophila
title_short Microbiome derived acidity protects against microbial invasion in Drosophila
title_sort microbiome derived acidity protects against microbial invasion in drosophila
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9882140/
https://www.ncbi.nlm.nih.gov/pubmed/36711873
http://dx.doi.org/10.1101/2023.01.12.523836
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