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dc.contributor.authorNelson, Paul G.
dc.contributor.authorMay, Georgiana
dc.date.accessioned2017-12-20T17:20:18Z
dc.date.available2017-12-20T17:20:18Z
dc.date.issued2017-12
dc.identifier.citationCoevolution between Mutualists and Parasites in Symbiotic Communities May Lead to the Evolution of Lower Virulence 2017, 190 (6):803 The American Naturalisten
dc.identifier.issn0003-0147
dc.identifier.issn1537-5323
dc.identifier.doi10.1086/694334
dc.identifier.urihttp://hdl.handle.net/10150/626255
dc.description.abstractMost eukaryotes harbor a diverse community of parasitic, mutualistic, and commensal microbial symbionts. Although the diversity of these microbial symbiotic communities has recently drawn considerable attention, theory regarding the evolution of interactions among symbionts and with the host is still in its nascent stages. Here we evaluate the role of interactions among coinfecting symbionts in the evolution of symbiont virulence toward the host. To do so, we place the virulence-transmission trade-off into a community context and model the evolution of symbiont trophic modes along the continuum from parasitism (virulence) to mutualism (negative virulence). We establish a framework for studying multiple infections of a host by the same symbiont species and coinfection by multiple species, using a concept of shared costs, wherein the negative consequences of virulence (or harm) toward the host are shared among symbionts. Our results show that mutualism can be maintained under infection by multiple symbionts when shared costs are sufficiently low, while greater virulence and parasitism toward the host are more likely when shared costs are high. Last, for coinfection by more than one species, we show that if the presence of a mutualist ameliorates some of the costs of pathogen virulence, then the symbiotic community may more often evolve to a more commensal state and maintain mutualisms.
dc.language.isoenen
dc.publisherUNIV CHICAGO PRESSen
dc.relation.urlhttp://www.journals.uchicago.edu/doi/10.1086/694334en
dc.rights© 2017 by The University of Chicago. All rights reserved. This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).en
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.subjectcoevolutionen
dc.subjectmutualismen
dc.subjectvirulenceen
dc.subjectsymbiosisen
dc.subjecttrade-offsen
dc.subjectparasitismen
dc.titleCoevolution between Mutualists and Parasites in Symbiotic Communities May Lead to the Evolution of Lower Virulenceen
dc.typeArticleen
dc.contributor.departmentUniv Arizona, Ecol & Evolutionary Biolen
dc.identifier.journalThe American Naturalisten
dc.description.note12 month embargo; Published online: 28 Sept 2017en
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.en
dc.eprint.versionFinal published versionen
html.description.abstractMost eukaryotes harbor a diverse community of parasitic, mutualistic, and commensal microbial symbionts. Although the diversity of these microbial symbiotic communities has recently drawn considerable attention, theory regarding the evolution of interactions among symbionts and with the host is still in its nascent stages. Here we evaluate the role of interactions among coinfecting symbionts in the evolution of symbiont virulence toward the host. To do so, we place the virulence-transmission trade-off into a community context and model the evolution of symbiont trophic modes along the continuum from parasitism (virulence) to mutualism (negative virulence). We establish a framework for studying multiple infections of a host by the same symbiont species and coinfection by multiple species, using a concept of shared costs, wherein the negative consequences of virulence (or harm) toward the host are shared among symbionts. Our results show that mutualism can be maintained under infection by multiple symbionts when shared costs are sufficiently low, while greater virulence and parasitism toward the host are more likely when shared costs are high. Last, for coinfection by more than one species, we show that if the presence of a mutualist ameliorates some of the costs of pathogen virulence, then the symbiotic community may more often evolve to a more commensal state and maintain mutualisms.


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© 2017 by The University of Chicago. All rights reserved. This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).
Except where otherwise noted, this item's license is described as © 2017 by The University of Chicago. All rights reserved. This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).