Evolutionarily Stable Coevolution Between a Plastic Lytic Virus and Its Microbial Host

Hosts influence and are influenced by viral replication. Cell size, for example, is a fundamental trait for microbial hosts that can not only alter the probability of viral adsorption, but also constrain the host physiological processes that the virus relies on to replicate. This intrinsic connectio...

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Main Authors: Melinda Choua, Michael R. Heath, Juan A. Bonachela
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-05-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmicb.2021.637490/full
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spelling doaj-ce722170220a4e39bbf3a5c0e58fb51b2021-05-20T05:36:34ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2021-05-011210.3389/fmicb.2021.637490637490Evolutionarily Stable Coevolution Between a Plastic Lytic Virus and Its Microbial HostMelinda Choua0Michael R. Heath1Juan A. Bonachela2Marine Population Modeling Group, Department of Mathematics and Statistics, University of Strathclyde, Scotland, United KingdomMarine Population Modeling Group, Department of Mathematics and Statistics, University of Strathclyde, Scotland, United KingdomDepartment of Ecology, Evolution and Natural Resources, Rutgers University, New Brunswick, NJ, United StatesHosts influence and are influenced by viral replication. Cell size, for example, is a fundamental trait for microbial hosts that can not only alter the probability of viral adsorption, but also constrain the host physiological processes that the virus relies on to replicate. This intrinsic connection can affect the fitness of both host and virus, and therefore their mutual evolution. Here, we study the coevolution of bacterial hosts and their viruses by considering the dependence of viral performance on the host physiological state (viral plasticity). To this end, we modified a standard host-lytic phage model to include viral plasticity, and compared the coevolutionary strategies emerging under different scenarios, including cases in which only the virus or the host evolve. For all cases, we also obtained the evolutionary prediction of the traditional version of the model, which assumes a non-plastic virus. Our results reveal that the presence of the virus leads to an increase in host size and growth rate in the long term, which benefits both interacting populations. Our results also show that viral plasticity and evolution influence the classic host quality-quantity trade-off. Poor nutrient environments lead to abundant low-quality hosts, which tends to increase viral infection time. Conversely, richer nutrient environments lead to fewer but high-quality hosts, which decrease viral infection time. Our results can contribute to advancing our understanding of the microbial response to changing environments. For instance, both cell size and viral-induced mortality are essential factors that determine the structure and dynamics of the marine microbial community, and therefore our study can improve predictions of how marine ecosystems respond to environmental change. Our study can also help devise more reliable strategies to use phage to, for example, fight bacterial infections.https://www.frontiersin.org/articles/10.3389/fmicb.2021.637490/fullphage (bacteriophage)virus modelinglysisviral latencyE. coliT phage
collection DOAJ
language English
format Article
sources DOAJ
author Melinda Choua
Michael R. Heath
Juan A. Bonachela
spellingShingle Melinda Choua
Michael R. Heath
Juan A. Bonachela
Evolutionarily Stable Coevolution Between a Plastic Lytic Virus and Its Microbial Host
Frontiers in Microbiology
phage (bacteriophage)
virus modeling
lysis
viral latency
E. coli
T phage
author_facet Melinda Choua
Michael R. Heath
Juan A. Bonachela
author_sort Melinda Choua
title Evolutionarily Stable Coevolution Between a Plastic Lytic Virus and Its Microbial Host
title_short Evolutionarily Stable Coevolution Between a Plastic Lytic Virus and Its Microbial Host
title_full Evolutionarily Stable Coevolution Between a Plastic Lytic Virus and Its Microbial Host
title_fullStr Evolutionarily Stable Coevolution Between a Plastic Lytic Virus and Its Microbial Host
title_full_unstemmed Evolutionarily Stable Coevolution Between a Plastic Lytic Virus and Its Microbial Host
title_sort evolutionarily stable coevolution between a plastic lytic virus and its microbial host
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2021-05-01
description Hosts influence and are influenced by viral replication. Cell size, for example, is a fundamental trait for microbial hosts that can not only alter the probability of viral adsorption, but also constrain the host physiological processes that the virus relies on to replicate. This intrinsic connection can affect the fitness of both host and virus, and therefore their mutual evolution. Here, we study the coevolution of bacterial hosts and their viruses by considering the dependence of viral performance on the host physiological state (viral plasticity). To this end, we modified a standard host-lytic phage model to include viral plasticity, and compared the coevolutionary strategies emerging under different scenarios, including cases in which only the virus or the host evolve. For all cases, we also obtained the evolutionary prediction of the traditional version of the model, which assumes a non-plastic virus. Our results reveal that the presence of the virus leads to an increase in host size and growth rate in the long term, which benefits both interacting populations. Our results also show that viral plasticity and evolution influence the classic host quality-quantity trade-off. Poor nutrient environments lead to abundant low-quality hosts, which tends to increase viral infection time. Conversely, richer nutrient environments lead to fewer but high-quality hosts, which decrease viral infection time. Our results can contribute to advancing our understanding of the microbial response to changing environments. For instance, both cell size and viral-induced mortality are essential factors that determine the structure and dynamics of the marine microbial community, and therefore our study can improve predictions of how marine ecosystems respond to environmental change. Our study can also help devise more reliable strategies to use phage to, for example, fight bacterial infections.
topic phage (bacteriophage)
virus modeling
lysis
viral latency
E. coli
T phage
url https://www.frontiersin.org/articles/10.3389/fmicb.2021.637490/full
work_keys_str_mv AT melindachoua evolutionarilystablecoevolutionbetweenaplasticlyticvirusanditsmicrobialhost
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