Coevolution between Mutualists and Parasites in Symbiotic Communities May Lead to the Evolution of Lower Virulence
Most 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 stil...
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description | Most 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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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.</description><identifier>ISSN: 0003-0147</identifier><identifier>EISSN: 1537-5323</identifier><identifier>DOI: 10.1086/694334</identifier><identifier>PMID: 29166166</identifier><language>eng</language><publisher>United States: The University of Chicago Press</publisher><subject>Animals ; Biodiversity ; Biological Evolution ; Coevolution ; Communities ; Concurrent infection ; Costs ; Eukaryotes ; Evolution ; Host-Pathogen Interactions ; Microorganisms ; Models, Biological ; Mutualism ; Parasites ; Parasitic diseases ; Parasitism ; Plant Diseases - microbiology ; Plants - microbiology ; Species ; Symbionts ; Symbiosis - physiology ; Virulence</subject><ispartof>The American naturalist, 2017-12, Vol.190 (6), p.803-817</ispartof><rights>2017 by The University of Chicago</rights><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), which permits non-commercial reuse of the work with attribution. For commercial use, contact .</rights><rights>Copyright University of Chicago, acting through its Press Dec 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-e87ecf74e118fc91769987ac19a0f55025779aef7a6571cc844e4cd78a71d1553</citedby><cites>FETCH-LOGICAL-c390t-e87ecf74e118fc91769987ac19a0f55025779aef7a6571cc844e4cd78a71d1553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/26521020$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/26521020$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29166166$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nelson, Paul G.</creatorcontrib><creatorcontrib>May, Georgiana</creatorcontrib><title>Coevolution between Mutualists and Parasites in Symbiotic Communities May Lead to the Evolution of Lower Virulence</title><title>The American naturalist</title><addtitle>Am Nat</addtitle><description>Most 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.</description><subject>Animals</subject><subject>Biodiversity</subject><subject>Biological Evolution</subject><subject>Coevolution</subject><subject>Communities</subject><subject>Concurrent infection</subject><subject>Costs</subject><subject>Eukaryotes</subject><subject>Evolution</subject><subject>Host-Pathogen Interactions</subject><subject>Microorganisms</subject><subject>Models, Biological</subject><subject>Mutualism</subject><subject>Parasites</subject><subject>Parasitic diseases</subject><subject>Parasitism</subject><subject>Plant Diseases - microbiology</subject><subject>Plants - microbiology</subject><subject>Species</subject><subject>Symbionts</subject><subject>Symbiosis - physiology</subject><subject>Virulence</subject><issn>0003-0147</issn><issn>1537-5323</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkW1LHDEQgINYvKvVf6AELKVftk02m2TzUQ61hROFtn5dctlZzbG7OfOi3L9vyp4nFAaGYR6eGWYQOqXkGyW1-C5UxVh1gOaUM1lwVrJDNCeEsILQSs7QxxDWuVSV4kdoVioqRI458gsHL65P0boRryC-Aoz4NsWkextiwHps8b32OtgIAdsR_9oOK-uiNXjhhiGNNtrcuNVbvATd4uhwfAJ8tXe6Di_dK3j8YH3qYTTwCX3odB_gZJeP0Z_rq9-LH8Xy7ubn4nJZGKZILKCWYDpZAaV1ZxSVQqlaakOVJh3npORSKg2d1IJLakxdVVCZVtZa0pZyzo7R18m78e45QYjNYIOBvtcjuBQaqoSsBSOEZvTiP3Ttkh_zdk3JpBC14iXJ1JeJMt6F4KFrNt4O2m8bSpp_X2imL2TwfKdLqwHaPfZ29gx8noBknqzRj27jIYT3oXvP2YStQ3T-XSN4SUle6C_1PZdx</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>Nelson, Paul G.</creator><creator>May, Georgiana</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><general>University of Chicago, acting through its Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope></search><sort><creationdate>20171201</creationdate><title>Coevolution between Mutualists and Parasites in Symbiotic Communities May Lead to the Evolution of Lower Virulence</title><author>Nelson, Paul G. ; May, Georgiana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-e87ecf74e118fc91769987ac19a0f55025779aef7a6571cc844e4cd78a71d1553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Biodiversity</topic><topic>Biological Evolution</topic><topic>Coevolution</topic><topic>Communities</topic><topic>Concurrent infection</topic><topic>Costs</topic><topic>Eukaryotes</topic><topic>Evolution</topic><topic>Host-Pathogen Interactions</topic><topic>Microorganisms</topic><topic>Models, Biological</topic><topic>Mutualism</topic><topic>Parasites</topic><topic>Parasitic diseases</topic><topic>Parasitism</topic><topic>Plant Diseases - microbiology</topic><topic>Plants - microbiology</topic><topic>Species</topic><topic>Symbionts</topic><topic>Symbiosis - physiology</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nelson, Paul G.</creatorcontrib><creatorcontrib>May, Georgiana</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The American naturalist</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nelson, Paul G.</au><au>May, Georgiana</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coevolution between Mutualists and Parasites in Symbiotic Communities May Lead to the Evolution of Lower Virulence</atitle><jtitle>The American naturalist</jtitle><addtitle>Am Nat</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>190</volume><issue>6</issue><spage>803</spage><epage>817</epage><pages>803-817</pages><issn>0003-0147</issn><eissn>1537-5323</eissn><abstract>Most 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.</abstract><cop>United States</cop><pub>The University of Chicago Press</pub><pmid>29166166</pmid><doi>10.1086/694334</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biodiversity Biological Evolution Coevolution Communities Concurrent infection Costs Eukaryotes Evolution Host-Pathogen Interactions Microorganisms Models, Biological Mutualism Parasites Parasitic diseases Parasitism Plant Diseases - microbiology Plants - microbiology Species Symbionts Symbiosis - physiology Virulence |
title | Coevolution between Mutualists and Parasites in Symbiotic Communities May Lead to the Evolution of Lower Virulence |
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