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Interaction variability shapes succession of synthetic microbial ecosystems

Cellular interactions are a major driver for the assembly and functioning of microbial communities. Their strengths are shown to be highly variable in nature; however, it is unclear how such variations regulate community behaviors. Here we construct synthetic Lactococcus lactis consortia and mathema...

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Autores principales: Liu, Feng, Mao, Junwen, Kong, Wentao, Hua, Qiang, Feng, Youjun, Bashir, Rashid, Lu, Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965111/
https://www.ncbi.nlm.nih.gov/pubmed/31949154
http://dx.doi.org/10.1038/s41467-019-13986-6
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author Liu, Feng
Mao, Junwen
Kong, Wentao
Hua, Qiang
Feng, Youjun
Bashir, Rashid
Lu, Ting
author_facet Liu, Feng
Mao, Junwen
Kong, Wentao
Hua, Qiang
Feng, Youjun
Bashir, Rashid
Lu, Ting
author_sort Liu, Feng
collection PubMed
description Cellular interactions are a major driver for the assembly and functioning of microbial communities. Their strengths are shown to be highly variable in nature; however, it is unclear how such variations regulate community behaviors. Here we construct synthetic Lactococcus lactis consortia and mathematical models to elucidate the role of interaction variability in ecosystem succession and to further determine if casting variability into modeling empowers bottom-up predictions. For a consortium of bacteriocin-mediated cooperation and competition, we find increasing the variations of cooperation, from either altered labor partition or random sampling, drives the community into distinct structures. When the cooperation and competition are additionally modulated by pH, ecosystem succession becomes jointly controlled by the variations of both interactions and yields more diversified dynamics. Mathematical models incorporating variability successfully capture all of these experimental observations. Our study demonstrates interaction variability as a key regulator of community dynamics, providing insights into bottom-up predictions of microbial ecosystems.
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spelling pubmed-69651112020-01-22 Interaction variability shapes succession of synthetic microbial ecosystems Liu, Feng Mao, Junwen Kong, Wentao Hua, Qiang Feng, Youjun Bashir, Rashid Lu, Ting Nat Commun Article Cellular interactions are a major driver for the assembly and functioning of microbial communities. Their strengths are shown to be highly variable in nature; however, it is unclear how such variations regulate community behaviors. Here we construct synthetic Lactococcus lactis consortia and mathematical models to elucidate the role of interaction variability in ecosystem succession and to further determine if casting variability into modeling empowers bottom-up predictions. For a consortium of bacteriocin-mediated cooperation and competition, we find increasing the variations of cooperation, from either altered labor partition or random sampling, drives the community into distinct structures. When the cooperation and competition are additionally modulated by pH, ecosystem succession becomes jointly controlled by the variations of both interactions and yields more diversified dynamics. Mathematical models incorporating variability successfully capture all of these experimental observations. Our study demonstrates interaction variability as a key regulator of community dynamics, providing insights into bottom-up predictions of microbial ecosystems. Nature Publishing Group UK 2020-01-16 /pmc/articles/PMC6965111/ /pubmed/31949154 http://dx.doi.org/10.1038/s41467-019-13986-6 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Liu, Feng
Mao, Junwen
Kong, Wentao
Hua, Qiang
Feng, Youjun
Bashir, Rashid
Lu, Ting
Interaction variability shapes succession of synthetic microbial ecosystems
title Interaction variability shapes succession of synthetic microbial ecosystems
title_full Interaction variability shapes succession of synthetic microbial ecosystems
title_fullStr Interaction variability shapes succession of synthetic microbial ecosystems
title_full_unstemmed Interaction variability shapes succession of synthetic microbial ecosystems
title_short Interaction variability shapes succession of synthetic microbial ecosystems
title_sort interaction variability shapes succession of synthetic microbial ecosystems
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965111/
https://www.ncbi.nlm.nih.gov/pubmed/31949154
http://dx.doi.org/10.1038/s41467-019-13986-6
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