Predators and Patterns of Within-Host Growth Can Mediate Both Among-Host Competition and Evolution of Transmission Potential of Parasites
Parasite prevalence shows tremendous spatiotemporal variation. Theory indicates that this variation might stem from life-history characteristics of parasites and key ecological factors. Here, we illustrate how the interaction of an important predator and the schedule of transmission potential of two...
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Veröffentlicht in: | The American naturalist 2014-08, Vol.184 (S1), p.S77-S90 |
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description | Parasite prevalence shows tremendous spatiotemporal variation. Theory indicates that this variation might stem from life-history characteristics of parasites and key ecological factors. Here, we illustrate how the interaction of an important predator and the schedule of transmission potential of two parasites can explain parasite abundance. A field survey showed that a noncastrating fungus (Metschnikowia bicuspidata) commonly infected a dominant zooplankton host (Daphnia dentifera), while a castrating bacterial parasite (Pasteuria ramosa) was rare. This result seemed surprising given that the bacterium produces many more infectious propagules (spores) than the fungus upon host death. The fungus’s dominance can be explained by the schedule of within-host growth of parasites (i.e., how transmission potential changes over the course of infection) and the release of spores from “sloppy” predators (Chaoborusspp., who consumeDaphniaprey whole and then later regurgitate the carapace and parasite spores). In essence, sloppy predators create a niche that the faster-schedule fungus currently occupies. However, a selection experiment showed that the slower-schedule bacterium can evolve into this faster-schedule, predator-mediated niche (but pays a cost in maximal spore yield to do so). Hence, our study shows how parasite life history can interact with predation to strongly influence the ecology, epidemiology, and evolution of infectious disease. |
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J. R. ; Hall, Spencer R. ; Housley Ochs, Jessica ; Sebastian, Mathew ; Duffy, Meghan A.</creator><contributor>Symposium Curtis M. Lively ; Curtis M. Lively</contributor><creatorcontrib>Auld, Stuart K. J. R. ; Hall, Spencer R. ; Housley Ochs, Jessica ; Sebastian, Mathew ; Duffy, Meghan A. ; Symposium Curtis M. Lively ; Curtis M. Lively</creatorcontrib><description>Parasite prevalence shows tremendous spatiotemporal variation. Theory indicates that this variation might stem from life-history characteristics of parasites and key ecological factors. Here, we illustrate how the interaction of an important predator and the schedule of transmission potential of two parasites can explain parasite abundance. A field survey showed that a noncastrating fungus (Metschnikowia bicuspidata) commonly infected a dominant zooplankton host (Daphnia dentifera), while a castrating bacterial parasite (Pasteuria ramosa) was rare. This result seemed surprising given that the bacterium produces many more infectious propagules (spores) than the fungus upon host death. The fungus’s dominance can be explained by the schedule of within-host growth of parasites (i.e., how transmission potential changes over the course of infection) and the release of spores from “sloppy” predators (Chaoborusspp., who consumeDaphniaprey whole and then later regurgitate the carapace and parasite spores). In essence, sloppy predators create a niche that the faster-schedule fungus currently occupies. However, a selection experiment showed that the slower-schedule bacterium can evolve into this faster-schedule, predator-mediated niche (but pays a cost in maximal spore yield to do so). Hence, our study shows how parasite life history can interact with predation to strongly influence the ecology, epidemiology, and evolution of infectious disease.</description><identifier>ISSN: 0003-0147</identifier><identifier>EISSN: 1537-5323</identifier><identifier>DOI: 10.1086/676927</identifier><identifier>PMID: 25061679</identifier><identifier>CODEN: AMNTA4</identifier><language>eng</language><publisher>United States: University of Chicago Press</publisher><subject>Animals ; Bacteria ; Bacterial spores ; Biological Evolution ; Chaoborus ; Chironomidae ; Daphnia ; Daphnia - microbiology ; Daphnia - parasitology ; Daphnia dentifera ; Ecological competition ; Ecology ; Epidemiology ; Freshwater ; Fungal spores ; Fungi ; Host-Pathogen Interactions - genetics ; Indiana ; Infections ; Infectious diseases ; Life Cycle Stages ; Metschnikowia - physiology ; Metschnikowia bicuspidata ; Michigan ; Obligate parasites ; Parasite hosts ; Parasites ; Pasteuria - genetics ; Pasteuria - pathogenicity ; Pasteuria ramosa ; Plankton ; Predation ; Predators ; Predatory Behavior</subject><ispartof>The American naturalist, 2014-08, Vol.184 (S1), p.S77-S90</ispartof><rights>2014 by The University of Chicago. 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A field survey showed that a noncastrating fungus (Metschnikowia bicuspidata) commonly infected a dominant zooplankton host (Daphnia dentifera), while a castrating bacterial parasite (Pasteuria ramosa) was rare. This result seemed surprising given that the bacterium produces many more infectious propagules (spores) than the fungus upon host death. The fungus’s dominance can be explained by the schedule of within-host growth of parasites (i.e., how transmission potential changes over the course of infection) and the release of spores from “sloppy” predators (Chaoborusspp., who consumeDaphniaprey whole and then later regurgitate the carapace and parasite spores). In essence, sloppy predators create a niche that the faster-schedule fungus currently occupies. However, a selection experiment showed that the slower-schedule bacterium can evolve into this faster-schedule, predator-mediated niche (but pays a cost in maximal spore yield to do so). Hence, our study shows how parasite life history can interact with predation to strongly influence the ecology, epidemiology, and evolution of infectious disease.</description><subject>Animals</subject><subject>Bacteria</subject><subject>Bacterial spores</subject><subject>Biological Evolution</subject><subject>Chaoborus</subject><subject>Chironomidae</subject><subject>Daphnia</subject><subject>Daphnia - microbiology</subject><subject>Daphnia - parasitology</subject><subject>Daphnia dentifera</subject><subject>Ecological competition</subject><subject>Ecology</subject><subject>Epidemiology</subject><subject>Freshwater</subject><subject>Fungal spores</subject><subject>Fungi</subject><subject>Host-Pathogen Interactions - genetics</subject><subject>Indiana</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Life Cycle Stages</subject><subject>Metschnikowia - physiology</subject><subject>Metschnikowia bicuspidata</subject><subject>Michigan</subject><subject>Obligate parasites</subject><subject>Parasite hosts</subject><subject>Parasites</subject><subject>Pasteuria - genetics</subject><subject>Pasteuria - pathogenicity</subject><subject>Pasteuria ramosa</subject><subject>Plankton</subject><subject>Predation</subject><subject>Predators</subject><subject>Predatory Behavior</subject><issn>0003-0147</issn><issn>1537-5323</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkt9qFDEYxYNY7Fr1EWRAEW9G8z-by7rUtlBxLypeDtlMpptlJhnzZRQfwbc226ldKAi9Cif5cXK-nCD0iuAPBC_lR6mkpuoJWhDBVC0YZU_RAmPMaky4OkbPAXZFaq7FM3RMBZZEKr1Af9bJtSbHBJUJbbU2ObsUoIpd9d3nrQ_1RYRcnaf4K2-rlQnVF9d6k131KZaN0yGGmxlZxWF02Wcfw63V2c_YT7eqeF0nE2DwAHu9jtmF7E2_P1mbZMBnBy_QUWd6cC_v1hP07fPZ9eqivvp6frk6vaotlzTXQrbYWot1a3FH-MaZJcGdoIxLpqwycsmZWjItidooWl5FaNEZuuHWGOWcZifo_ew7pvhjcpCbksu6vjfBxQkaIiQmlCkuHoFyTbQmau_65gG6i1MKZZBCCUp4yYML9W6mbIoAyXXNmPxg0u-G4GbfYzP3WMDXd3bTZnDtPfavuEO0yW69NTdxTA7gcOns04xtV9C3j0APE-ygfIf_BfsLZ8O9Pg</recordid><startdate>20140801</startdate><enddate>20140801</enddate><creator>Auld, Stuart K. 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R. ; Hall, Spencer R. ; Housley Ochs, Jessica ; Sebastian, Mathew ; Duffy, Meghan A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-56d0ccc09dc0f14bea810f5234637c7a68437839617b72769595fa2b4caa7ee93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Bacteria</topic><topic>Bacterial spores</topic><topic>Biological Evolution</topic><topic>Chaoborus</topic><topic>Chironomidae</topic><topic>Daphnia</topic><topic>Daphnia - microbiology</topic><topic>Daphnia - parasitology</topic><topic>Daphnia dentifera</topic><topic>Ecological competition</topic><topic>Ecology</topic><topic>Epidemiology</topic><topic>Freshwater</topic><topic>Fungal spores</topic><topic>Fungi</topic><topic>Host-Pathogen Interactions - genetics</topic><topic>Indiana</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Life Cycle Stages</topic><topic>Metschnikowia - physiology</topic><topic>Metschnikowia bicuspidata</topic><topic>Michigan</topic><topic>Obligate parasites</topic><topic>Parasite hosts</topic><topic>Parasites</topic><topic>Pasteuria - genetics</topic><topic>Pasteuria - pathogenicity</topic><topic>Pasteuria ramosa</topic><topic>Plankton</topic><topic>Predation</topic><topic>Predators</topic><topic>Predatory Behavior</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Auld, Stuart K. 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R.</creatorcontrib><creatorcontrib>Hall, Spencer R.</creatorcontrib><creatorcontrib>Housley Ochs, Jessica</creatorcontrib><creatorcontrib>Sebastian, Mathew</creatorcontrib><creatorcontrib>Duffy, Meghan A.</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><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>The American naturalist</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Auld, Stuart K. J. R.</au><au>Hall, Spencer R.</au><au>Housley Ochs, Jessica</au><au>Sebastian, Mathew</au><au>Duffy, Meghan A.</au><au>Symposium Curtis M. Lively</au><au>Curtis M. Lively</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predators and Patterns of Within-Host Growth Can Mediate Both Among-Host Competition and Evolution of Transmission Potential of Parasites</atitle><jtitle>The American naturalist</jtitle><addtitle>Am Nat</addtitle><date>2014-08-01</date><risdate>2014</risdate><volume>184</volume><issue>S1</issue><spage>S77</spage><epage>S90</epage><pages>S77-S90</pages><issn>0003-0147</issn><eissn>1537-5323</eissn><coden>AMNTA4</coden><abstract>Parasite prevalence shows tremendous spatiotemporal variation. Theory indicates that this variation might stem from life-history characteristics of parasites and key ecological factors. Here, we illustrate how the interaction of an important predator and the schedule of transmission potential of two parasites can explain parasite abundance. A field survey showed that a noncastrating fungus (Metschnikowia bicuspidata) commonly infected a dominant zooplankton host (Daphnia dentifera), while a castrating bacterial parasite (Pasteuria ramosa) was rare. This result seemed surprising given that the bacterium produces many more infectious propagules (spores) than the fungus upon host death. The fungus’s dominance can be explained by the schedule of within-host growth of parasites (i.e., how transmission potential changes over the course of infection) and the release of spores from “sloppy” predators (Chaoborusspp., who consumeDaphniaprey whole and then later regurgitate the carapace and parasite spores). In essence, sloppy predators create a niche that the faster-schedule fungus currently occupies. However, a selection experiment showed that the slower-schedule bacterium can evolve into this faster-schedule, predator-mediated niche (but pays a cost in maximal spore yield to do so). Hence, our study shows how parasite life history can interact with predation to strongly influence the ecology, epidemiology, and evolution of infectious disease.</abstract><cop>United States</cop><pub>University of Chicago Press</pub><pmid>25061679</pmid><doi>10.1086/676927</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Bacteria Bacterial spores Biological Evolution Chaoborus Chironomidae Daphnia Daphnia - microbiology Daphnia - parasitology Daphnia dentifera Ecological competition Ecology Epidemiology Freshwater Fungal spores Fungi Host-Pathogen Interactions - genetics Indiana Infections Infectious diseases Life Cycle Stages Metschnikowia - physiology Metschnikowia bicuspidata Michigan Obligate parasites Parasite hosts Parasites Pasteuria - genetics Pasteuria - pathogenicity Pasteuria ramosa Plankton Predation Predators Predatory Behavior |
title | Predators and Patterns of Within-Host Growth Can Mediate Both Among-Host Competition and Evolution of Transmission Potential of Parasites |
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