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Controlling evolutionary dynamics to optimize microbial bioremediation

Some microbes have a fascinating ability to degrade compounds that are toxic for humans in a process called bioremediation. Although these traits help microbes survive the toxins, carrying them can be costly if the benefit of detoxification is shared by all surrounding microbes, whether they detoxif...

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Detalles Bibliográficos
Autores principales: Shibasaki, Shota, Mitri, Sara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7513707/
https://www.ncbi.nlm.nih.gov/pubmed/33005234
http://dx.doi.org/10.1111/eva.13050
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author Shibasaki, Shota
Mitri, Sara
author_facet Shibasaki, Shota
Mitri, Sara
author_sort Shibasaki, Shota
collection PubMed
description Some microbes have a fascinating ability to degrade compounds that are toxic for humans in a process called bioremediation. Although these traits help microbes survive the toxins, carrying them can be costly if the benefit of detoxification is shared by all surrounding microbes, whether they detoxify or not. Detoxification can thereby be seen as a public goods game, where nondegrading mutants can sweep through the population and collapse bioremediation. Here, we constructed an evolutionary game theoretical model to optimize bioremediation in a chemostat initially containing “cooperating” (detoxifying) microbes. We consider two types of mutants: “cheaters” that do not detoxify, and mutants that become resistant to the toxin through private mechanisms that do not benefit others. By manipulating the concentration and flow rate of a toxin into the chemostat, we identified conditions where cooperators can exclude cheaters that differ in their private resistance. However, eventually, cheaters are bound to invade. To overcome this inevitable outcome and maximize detoxification efficiency, cooperators can be periodically reinoculated into the population. Our study investigates the outcome of an evolutionary game combining both public and private goods and demonstrates how environmental parameters can be used to control evolutionary dynamics in practical applications.
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spelling pubmed-75137072020-09-30 Controlling evolutionary dynamics to optimize microbial bioremediation Shibasaki, Shota Mitri, Sara Evol Appl Original Articles Some microbes have a fascinating ability to degrade compounds that are toxic for humans in a process called bioremediation. Although these traits help microbes survive the toxins, carrying them can be costly if the benefit of detoxification is shared by all surrounding microbes, whether they detoxify or not. Detoxification can thereby be seen as a public goods game, where nondegrading mutants can sweep through the population and collapse bioremediation. Here, we constructed an evolutionary game theoretical model to optimize bioremediation in a chemostat initially containing “cooperating” (detoxifying) microbes. We consider two types of mutants: “cheaters” that do not detoxify, and mutants that become resistant to the toxin through private mechanisms that do not benefit others. By manipulating the concentration and flow rate of a toxin into the chemostat, we identified conditions where cooperators can exclude cheaters that differ in their private resistance. However, eventually, cheaters are bound to invade. To overcome this inevitable outcome and maximize detoxification efficiency, cooperators can be periodically reinoculated into the population. Our study investigates the outcome of an evolutionary game combining both public and private goods and demonstrates how environmental parameters can be used to control evolutionary dynamics in practical applications. John Wiley and Sons Inc. 2020-07-28 /pmc/articles/PMC7513707/ /pubmed/33005234 http://dx.doi.org/10.1111/eva.13050 Text en © 2020 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Shibasaki, Shota
Mitri, Sara
Controlling evolutionary dynamics to optimize microbial bioremediation
title Controlling evolutionary dynamics to optimize microbial bioremediation
title_full Controlling evolutionary dynamics to optimize microbial bioremediation
title_fullStr Controlling evolutionary dynamics to optimize microbial bioremediation
title_full_unstemmed Controlling evolutionary dynamics to optimize microbial bioremediation
title_short Controlling evolutionary dynamics to optimize microbial bioremediation
title_sort controlling evolutionary dynamics to optimize microbial bioremediation
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7513707/
https://www.ncbi.nlm.nih.gov/pubmed/33005234
http://dx.doi.org/10.1111/eva.13050
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