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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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. |
format | Online Article Text |
id | pubmed-6965111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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