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Global dynamics of microbial communities emerge from local interaction rules

Most microbes live in spatially structured communities (e.g., biofilms) in which they interact with their neighbors through the local exchange of diffusible molecules. To understand the functioning of these communities, it is essential to uncover how these local interactions shape community-level pr...

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Autores principales: van Vliet, Simon, Hauert, Christoph, Fridberg, Kyle, Ackermann, Martin, Dal Co, Alma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8926250/
https://www.ncbi.nlm.nih.gov/pubmed/35245282
http://dx.doi.org/10.1371/journal.pcbi.1009877
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author van Vliet, Simon
Hauert, Christoph
Fridberg, Kyle
Ackermann, Martin
Dal Co, Alma
author_facet van Vliet, Simon
Hauert, Christoph
Fridberg, Kyle
Ackermann, Martin
Dal Co, Alma
author_sort van Vliet, Simon
collection PubMed
description Most microbes live in spatially structured communities (e.g., biofilms) in which they interact with their neighbors through the local exchange of diffusible molecules. To understand the functioning of these communities, it is essential to uncover how these local interactions shape community-level properties, such as the community composition, spatial arrangement, and growth rate. Here, we present a mathematical framework to derive community-level properties from the molecular mechanisms underlying the cell-cell interactions for systems consisting of two cell types. Our framework consists of two parts: a biophysical model to derive the local interaction rules (i.e. interaction range and strength) from the molecular parameters underlying the cell-cell interactions and a graph based model to derive the equilibrium properties of the community (i.e. composition, spatial arrangement, and growth rate) from these local interaction rules. Our framework shows that key molecular parameters underlying the cell-cell interactions (e.g., the uptake and leakage rates of molecules) determine community-level properties. We apply our model to mutualistic cross-feeding communities and show that spatial structure can be detrimental for these communities. Moreover, our model can qualitatively recapitulate the properties of an experimental microbial community. Our framework can be extended to a variety of systems of two interacting cell types, within and beyond the microbial world, and contributes to our understanding of how community-level properties emerge from microscopic interactions between cells.
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spelling pubmed-89262502022-03-17 Global dynamics of microbial communities emerge from local interaction rules van Vliet, Simon Hauert, Christoph Fridberg, Kyle Ackermann, Martin Dal Co, Alma PLoS Comput Biol Research Article Most microbes live in spatially structured communities (e.g., biofilms) in which they interact with their neighbors through the local exchange of diffusible molecules. To understand the functioning of these communities, it is essential to uncover how these local interactions shape community-level properties, such as the community composition, spatial arrangement, and growth rate. Here, we present a mathematical framework to derive community-level properties from the molecular mechanisms underlying the cell-cell interactions for systems consisting of two cell types. Our framework consists of two parts: a biophysical model to derive the local interaction rules (i.e. interaction range and strength) from the molecular parameters underlying the cell-cell interactions and a graph based model to derive the equilibrium properties of the community (i.e. composition, spatial arrangement, and growth rate) from these local interaction rules. Our framework shows that key molecular parameters underlying the cell-cell interactions (e.g., the uptake and leakage rates of molecules) determine community-level properties. We apply our model to mutualistic cross-feeding communities and show that spatial structure can be detrimental for these communities. Moreover, our model can qualitatively recapitulate the properties of an experimental microbial community. Our framework can be extended to a variety of systems of two interacting cell types, within and beyond the microbial world, and contributes to our understanding of how community-level properties emerge from microscopic interactions between cells. Public Library of Science 2022-03-04 /pmc/articles/PMC8926250/ /pubmed/35245282 http://dx.doi.org/10.1371/journal.pcbi.1009877 Text en © 2022 van Vliet et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
van Vliet, Simon
Hauert, Christoph
Fridberg, Kyle
Ackermann, Martin
Dal Co, Alma
Global dynamics of microbial communities emerge from local interaction rules
title Global dynamics of microbial communities emerge from local interaction rules
title_full Global dynamics of microbial communities emerge from local interaction rules
title_fullStr Global dynamics of microbial communities emerge from local interaction rules
title_full_unstemmed Global dynamics of microbial communities emerge from local interaction rules
title_short Global dynamics of microbial communities emerge from local interaction rules
title_sort global dynamics of microbial communities emerge from local interaction rules
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8926250/
https://www.ncbi.nlm.nih.gov/pubmed/35245282
http://dx.doi.org/10.1371/journal.pcbi.1009877
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