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Spatial structure favors microbial coexistence except when slower mediator diffusion weakens interactions

Microbes often exist in spatially structured environments and many of their interactions are mediated through diffusible metabolites. How does such a context affect microbial coexistence? To address this question, we use a model in which the spatial distributions of species and diffusible interactio...

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Autores principales: Lobanov, Alexander, Dyckman, Samantha, Kurkjian, Helen, Momeni, Babak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10348751/
https://www.ncbi.nlm.nih.gov/pubmed/37350317
http://dx.doi.org/10.7554/eLife.82504
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author Lobanov, Alexander
Dyckman, Samantha
Kurkjian, Helen
Momeni, Babak
author_facet Lobanov, Alexander
Dyckman, Samantha
Kurkjian, Helen
Momeni, Babak
author_sort Lobanov, Alexander
collection PubMed
description Microbes often exist in spatially structured environments and many of their interactions are mediated through diffusible metabolites. How does such a context affect microbial coexistence? To address this question, we use a model in which the spatial distributions of species and diffusible interaction mediators are explicitly included. We simulate the enrichment process, examining how microbial species spatially reorganize and how eventually a subset of them coexist. In our model, we find that slower motility of cells promotes coexistence by allowing species to co-localize with their facilitators and avoid their inhibitors. We additionally find that a spatially structured environment is more influential when species mostly facilitate each other, rather than when they are mostly competing. More coexistence is observed when species produce many mediators and consume some (not many or few) mediators, and when overall consumption and production rates are balanced. Interestingly, coexistence appears to be disfavored when mediators are diffusing slowly because that leads to weaker interaction strengths. Overall, our results offer new insights into how production, consumption, motility, and diffusion intersect to determine microbial coexistence in a spatially structured environment.
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spelling pubmed-103487512023-07-15 Spatial structure favors microbial coexistence except when slower mediator diffusion weakens interactions Lobanov, Alexander Dyckman, Samantha Kurkjian, Helen Momeni, Babak eLife Computational and Systems Biology Microbes often exist in spatially structured environments and many of their interactions are mediated through diffusible metabolites. How does such a context affect microbial coexistence? To address this question, we use a model in which the spatial distributions of species and diffusible interaction mediators are explicitly included. We simulate the enrichment process, examining how microbial species spatially reorganize and how eventually a subset of them coexist. In our model, we find that slower motility of cells promotes coexistence by allowing species to co-localize with their facilitators and avoid their inhibitors. We additionally find that a spatially structured environment is more influential when species mostly facilitate each other, rather than when they are mostly competing. More coexistence is observed when species produce many mediators and consume some (not many or few) mediators, and when overall consumption and production rates are balanced. Interestingly, coexistence appears to be disfavored when mediators are diffusing slowly because that leads to weaker interaction strengths. Overall, our results offer new insights into how production, consumption, motility, and diffusion intersect to determine microbial coexistence in a spatially structured environment. eLife Sciences Publications, Ltd 2023-06-23 /pmc/articles/PMC10348751/ /pubmed/37350317 http://dx.doi.org/10.7554/eLife.82504 Text en © 2023, Lobanov, Dyckman 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 Computational and Systems Biology
Lobanov, Alexander
Dyckman, Samantha
Kurkjian, Helen
Momeni, Babak
Spatial structure favors microbial coexistence except when slower mediator diffusion weakens interactions
title Spatial structure favors microbial coexistence except when slower mediator diffusion weakens interactions
title_full Spatial structure favors microbial coexistence except when slower mediator diffusion weakens interactions
title_fullStr Spatial structure favors microbial coexistence except when slower mediator diffusion weakens interactions
title_full_unstemmed Spatial structure favors microbial coexistence except when slower mediator diffusion weakens interactions
title_short Spatial structure favors microbial coexistence except when slower mediator diffusion weakens interactions
title_sort spatial structure favors microbial coexistence except when slower mediator diffusion weakens interactions
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10348751/
https://www.ncbi.nlm.nih.gov/pubmed/37350317
http://dx.doi.org/10.7554/eLife.82504
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AT kurkjianhelen spatialstructurefavorsmicrobialcoexistenceexceptwhenslowermediatordiffusionweakensinteractions
AT momenibabak spatialstructurefavorsmicrobialcoexistenceexceptwhenslowermediatordiffusionweakensinteractions