Modeling microbial metabolic trade-offs in a chemostat.

Microbes face intense competition in the natural world, and so need to wisely allocate their resources to multiple functions, in particular to metabolism. Understanding competition among metabolic strategies that are subject to trade-offs is therefore crucial for deeper insight into the competition,...

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Main Authors: Zhiyuan Li, Bo Liu, Sophia Hsin-Jung Li, Christopher G King, Zemer Gitai, Ned S Wingreen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-08-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1008156
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spelling doaj-15bf27c00c724da3bf30d21c830f3f8c2021-04-21T15:17:42ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582020-08-01168e100815610.1371/journal.pcbi.1008156Modeling microbial metabolic trade-offs in a chemostat.Zhiyuan LiBo LiuSophia Hsin-Jung LiChristopher G KingZemer GitaiNed S WingreenMicrobes face intense competition in the natural world, and so need to wisely allocate their resources to multiple functions, in particular to metabolism. Understanding competition among metabolic strategies that are subject to trade-offs is therefore crucial for deeper insight into the competition, cooperation, and community assembly of microorganisms. In this work, we evaluate competing metabolic strategies within an ecological context by considering not only how the environment influences cell growth, but also how microbes shape their chemical environment. Utilizing chemostat-based resource-competition models, we exhibit a set of intuitive and general procedures for assessing metabolic strategies. Using this framework, we are able to relate and unify multiple metabolic models, and to demonstrate how the fitness landscape of strategies becomes intrinsically dynamic due to species-environment feedback. Such dynamic fitness landscapes produce rich behaviors, and prove to be crucial for ecological and evolutionarily stable coexistence in all the models we examined.https://doi.org/10.1371/journal.pcbi.1008156
collection DOAJ
language English
format Article
sources DOAJ
author Zhiyuan Li
Bo Liu
Sophia Hsin-Jung Li
Christopher G King
Zemer Gitai
Ned S Wingreen
spellingShingle Zhiyuan Li
Bo Liu
Sophia Hsin-Jung Li
Christopher G King
Zemer Gitai
Ned S Wingreen
Modeling microbial metabolic trade-offs in a chemostat.
PLoS Computational Biology
author_facet Zhiyuan Li
Bo Liu
Sophia Hsin-Jung Li
Christopher G King
Zemer Gitai
Ned S Wingreen
author_sort Zhiyuan Li
title Modeling microbial metabolic trade-offs in a chemostat.
title_short Modeling microbial metabolic trade-offs in a chemostat.
title_full Modeling microbial metabolic trade-offs in a chemostat.
title_fullStr Modeling microbial metabolic trade-offs in a chemostat.
title_full_unstemmed Modeling microbial metabolic trade-offs in a chemostat.
title_sort modeling microbial metabolic trade-offs in a chemostat.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2020-08-01
description Microbes face intense competition in the natural world, and so need to wisely allocate their resources to multiple functions, in particular to metabolism. Understanding competition among metabolic strategies that are subject to trade-offs is therefore crucial for deeper insight into the competition, cooperation, and community assembly of microorganisms. In this work, we evaluate competing metabolic strategies within an ecological context by considering not only how the environment influences cell growth, but also how microbes shape their chemical environment. Utilizing chemostat-based resource-competition models, we exhibit a set of intuitive and general procedures for assessing metabolic strategies. Using this framework, we are able to relate and unify multiple metabolic models, and to demonstrate how the fitness landscape of strategies becomes intrinsically dynamic due to species-environment feedback. Such dynamic fitness landscapes produce rich behaviors, and prove to be crucial for ecological and evolutionarily stable coexistence in all the models we examined.
url https://doi.org/10.1371/journal.pcbi.1008156
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