Cargando…

Modulation of microbial community dynamics by spatial partitioning

Microbial communities inhabit spatial architectures that divide a global environment into isolated or semi-isolated local environments, which leads to the partitioning of a microbial community into a collection of local communities. Despite its ubiquity and great interest in related processes, how a...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Feilun, Ha, Yuanchi, Weiss, Andrea, Wang, Meidi, Letourneau, Jeffrey, Wang, Shangying, Luo, Nan, Huang, Shuquan, Lee, Charlotte T., David, Lawrence, You, Lingchong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8967799/
https://www.ncbi.nlm.nih.gov/pubmed/35145274
http://dx.doi.org/10.1038/s41589-021-00961-w
_version_ 1784678904777146368
author Wu, Feilun
Ha, Yuanchi
Weiss, Andrea
Wang, Meidi
Letourneau, Jeffrey
Wang, Shangying
Luo, Nan
Huang, Shuquan
Lee, Charlotte T.
David, Lawrence
You, Lingchong
author_facet Wu, Feilun
Ha, Yuanchi
Weiss, Andrea
Wang, Meidi
Letourneau, Jeffrey
Wang, Shangying
Luo, Nan
Huang, Shuquan
Lee, Charlotte T.
David, Lawrence
You, Lingchong
author_sort Wu, Feilun
collection PubMed
description Microbial communities inhabit spatial architectures that divide a global environment into isolated or semi-isolated local environments, which leads to the partitioning of a microbial community into a collection of local communities. Despite its ubiquity and great interest in related processes, how and to what extent spatial partitioning affects the structures and dynamics of microbial communities is poorly understood. Using modeling and quantitative experiments with simple and complex microbial communities, we demonstrate that spatial partitioning modulates the community dynamics by altering the local interaction types and global interaction strength. Partitioning promotes the persistence of populations with negative interactions but suppresses those with positive interactions. For a community consisting of populations with both positive and negative interactions, an intermediate level of partitioning maximizes the overall diversity of the community. Our results reveal a general mechanism underlying the maintenance of microbial diversity and have implications for natural and engineered communities.
format Online
Article
Text
id pubmed-8967799
institution National Center for Biotechnology Information
language English
publishDate 2022
record_format MEDLINE/PubMed
spelling pubmed-89677992022-08-10 Modulation of microbial community dynamics by spatial partitioning Wu, Feilun Ha, Yuanchi Weiss, Andrea Wang, Meidi Letourneau, Jeffrey Wang, Shangying Luo, Nan Huang, Shuquan Lee, Charlotte T. David, Lawrence You, Lingchong Nat Chem Biol Article Microbial communities inhabit spatial architectures that divide a global environment into isolated or semi-isolated local environments, which leads to the partitioning of a microbial community into a collection of local communities. Despite its ubiquity and great interest in related processes, how and to what extent spatial partitioning affects the structures and dynamics of microbial communities is poorly understood. Using modeling and quantitative experiments with simple and complex microbial communities, we demonstrate that spatial partitioning modulates the community dynamics by altering the local interaction types and global interaction strength. Partitioning promotes the persistence of populations with negative interactions but suppresses those with positive interactions. For a community consisting of populations with both positive and negative interactions, an intermediate level of partitioning maximizes the overall diversity of the community. Our results reveal a general mechanism underlying the maintenance of microbial diversity and have implications for natural and engineered communities. 2022-04 2022-02-10 /pmc/articles/PMC8967799/ /pubmed/35145274 http://dx.doi.org/10.1038/s41589-021-00961-w Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: https://www.springernature.com/gp/open-research/policies/accepted-manuscript-terms
spellingShingle Article
Wu, Feilun
Ha, Yuanchi
Weiss, Andrea
Wang, Meidi
Letourneau, Jeffrey
Wang, Shangying
Luo, Nan
Huang, Shuquan
Lee, Charlotte T.
David, Lawrence
You, Lingchong
Modulation of microbial community dynamics by spatial partitioning
title Modulation of microbial community dynamics by spatial partitioning
title_full Modulation of microbial community dynamics by spatial partitioning
title_fullStr Modulation of microbial community dynamics by spatial partitioning
title_full_unstemmed Modulation of microbial community dynamics by spatial partitioning
title_short Modulation of microbial community dynamics by spatial partitioning
title_sort modulation of microbial community dynamics by spatial partitioning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8967799/
https://www.ncbi.nlm.nih.gov/pubmed/35145274
http://dx.doi.org/10.1038/s41589-021-00961-w
work_keys_str_mv AT wufeilun modulationofmicrobialcommunitydynamicsbyspatialpartitioning
AT hayuanchi modulationofmicrobialcommunitydynamicsbyspatialpartitioning
AT weissandrea modulationofmicrobialcommunitydynamicsbyspatialpartitioning
AT wangmeidi modulationofmicrobialcommunitydynamicsbyspatialpartitioning
AT letourneaujeffrey modulationofmicrobialcommunitydynamicsbyspatialpartitioning
AT wangshangying modulationofmicrobialcommunitydynamicsbyspatialpartitioning
AT luonan modulationofmicrobialcommunitydynamicsbyspatialpartitioning
AT huangshuquan modulationofmicrobialcommunitydynamicsbyspatialpartitioning
AT leecharlottet modulationofmicrobialcommunitydynamicsbyspatialpartitioning
AT davidlawrence modulationofmicrobialcommunitydynamicsbyspatialpartitioning
AT youlingchong modulationofmicrobialcommunitydynamicsbyspatialpartitioning