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Evolutionary modeling suggests that addictions may be driven by competition-induced microbiome dysbiosis

Recent studies revealed mechanisms by which the microbiome affects its host’s brain, behavior and wellbeing, and that dysbiosis – persistent microbiome-imbalance – is associated with the onset and progress of various chronic diseases, including addictive behaviors. Yet, understanding of the ecologic...

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Autores principales: Lewin-Epstein, Ohad, Jaques, Yanabah, Feldman, Marcus W., Kaufer, Daniela, Hadany, Lilach
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372008/
https://www.ncbi.nlm.nih.gov/pubmed/37495841
http://dx.doi.org/10.1038/s42003-023-05099-0
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author Lewin-Epstein, Ohad
Jaques, Yanabah
Feldman, Marcus W.
Kaufer, Daniela
Hadany, Lilach
author_facet Lewin-Epstein, Ohad
Jaques, Yanabah
Feldman, Marcus W.
Kaufer, Daniela
Hadany, Lilach
author_sort Lewin-Epstein, Ohad
collection PubMed
description Recent studies revealed mechanisms by which the microbiome affects its host’s brain, behavior and wellbeing, and that dysbiosis – persistent microbiome-imbalance – is associated with the onset and progress of various chronic diseases, including addictive behaviors. Yet, understanding of the ecological and evolutionary processes that shape the host-microbiome ecosystem and affect the host state, is still limited. Here we propose that competition dynamics within the microbiome, associated with host-microbiome mutual regulation, may promote dysbiosis and aggravate addictive behaviors. We construct a mathematical framework, modeling the dynamics of the host-microbiome ecosystem in response to alterations. We find that when this ecosystem is exposed to substantial perturbations, the microbiome may shift towards a composition that reinforces the new host state. Such a positive feedback loop augments post-perturbation imbalances, hindering attempts to return to the initial equilibrium, promoting relapse episodes and prolonging addictions. We show that the initial microbiome composition is a key factor: a diverse microbiome enhances the ecosystem’s resilience, whereas lower microbiome diversity is more prone to lead to dysbiosis, exacerbating addictions. This framework provides evolutionary and ecological perspectives on host-microbiome interactions and their implications for host behavior and health, while offering verifiable predictions with potential relevance to clinical treatments.
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spelling pubmed-103720082023-07-28 Evolutionary modeling suggests that addictions may be driven by competition-induced microbiome dysbiosis Lewin-Epstein, Ohad Jaques, Yanabah Feldman, Marcus W. Kaufer, Daniela Hadany, Lilach Commun Biol Article Recent studies revealed mechanisms by which the microbiome affects its host’s brain, behavior and wellbeing, and that dysbiosis – persistent microbiome-imbalance – is associated with the onset and progress of various chronic diseases, including addictive behaviors. Yet, understanding of the ecological and evolutionary processes that shape the host-microbiome ecosystem and affect the host state, is still limited. Here we propose that competition dynamics within the microbiome, associated with host-microbiome mutual regulation, may promote dysbiosis and aggravate addictive behaviors. We construct a mathematical framework, modeling the dynamics of the host-microbiome ecosystem in response to alterations. We find that when this ecosystem is exposed to substantial perturbations, the microbiome may shift towards a composition that reinforces the new host state. Such a positive feedback loop augments post-perturbation imbalances, hindering attempts to return to the initial equilibrium, promoting relapse episodes and prolonging addictions. We show that the initial microbiome composition is a key factor: a diverse microbiome enhances the ecosystem’s resilience, whereas lower microbiome diversity is more prone to lead to dysbiosis, exacerbating addictions. This framework provides evolutionary and ecological perspectives on host-microbiome interactions and their implications for host behavior and health, while offering verifiable predictions with potential relevance to clinical treatments. Nature Publishing Group UK 2023-07-26 /pmc/articles/PMC10372008/ /pubmed/37495841 http://dx.doi.org/10.1038/s42003-023-05099-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lewin-Epstein, Ohad
Jaques, Yanabah
Feldman, Marcus W.
Kaufer, Daniela
Hadany, Lilach
Evolutionary modeling suggests that addictions may be driven by competition-induced microbiome dysbiosis
title Evolutionary modeling suggests that addictions may be driven by competition-induced microbiome dysbiosis
title_full Evolutionary modeling suggests that addictions may be driven by competition-induced microbiome dysbiosis
title_fullStr Evolutionary modeling suggests that addictions may be driven by competition-induced microbiome dysbiosis
title_full_unstemmed Evolutionary modeling suggests that addictions may be driven by competition-induced microbiome dysbiosis
title_short Evolutionary modeling suggests that addictions may be driven by competition-induced microbiome dysbiosis
title_sort evolutionary modeling suggests that addictions may be driven by competition-induced microbiome dysbiosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372008/
https://www.ncbi.nlm.nih.gov/pubmed/37495841
http://dx.doi.org/10.1038/s42003-023-05099-0
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