Loading…

Behavioural fever reduces ranaviral infection in toads

Host behaviour is known to influence disease dynamics. Additionally, hosts often change their behaviours in response to pathogen detection to resist and avoid disease. The capacity of wildlife populations to respond to pathogens using behavioural plasticity is critical for reducing the impacts of di...

Full description

Saved in:
Bibliographic Details
Published in:Functional ecology 2019-11, Vol.33 (11), p.2172-2179
Main Authors: Sauer, Erin L., Trejo, Nadia, Hoverman, Jason T., Rohr, Jason R., Pedersen, Amy
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c4677-d110b3ccdeb1098b6065a9272eb95d6ed75e35c056cd8fee60f4d0661bd437553
cites cdi_FETCH-LOGICAL-c4677-d110b3ccdeb1098b6065a9272eb95d6ed75e35c056cd8fee60f4d0661bd437553
container_end_page 2179
container_issue 11
container_start_page 2172
container_title Functional ecology
container_volume 33
creator Sauer, Erin L.
Trejo, Nadia
Hoverman, Jason T.
Rohr, Jason R.
Pedersen, Amy
description Host behaviour is known to influence disease dynamics. Additionally, hosts often change their behaviours in response to pathogen detection to resist and avoid disease. The capacity of wildlife populations to respond to pathogens using behavioural plasticity is critical for reducing the impacts of disease outbreaks. However, there is limited information regarding the ability of ectothermic vertebrates to resist diseases via behavioural plasticity. Here, we experimentally examine the effect of host behaviour on ranaviral infections, which affect at least 175 species of ectothermic vertebrates. We placed metamorphic (temporal block 1) or adult (block 2) southern toads (Anaxyrus terrestris) in thermal gradients, tested their temperature preferences before and after oral inoculation by measuring individual‐level body temperature over time, and measured ranaviral loads of viral‐exposed individuals. We found significant individual‐level variation in temperature preference and evidence for behavioural fever in both metamorphic and adult A. terrestris during the first 2 days after exposure. Additionally, we found that individual‐level change in temperature preference was negatively correlated with ranaviral load and a better predictor of load than average temperature preference or maximum temperature reached by an individual. In other words, an increase in baseline temperature preference was more important than simply reaching an absolute temperature. These results suggest that behavioural fever is an effective mechanism for resisting ranaviral infections. A free Plain Language Summary can be found within the Supporting Information of this article. A free Plain Language Summary can be found within the Supporting Information of this article.
doi_str_mv 10.1111/1365-2435.13427
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7546308</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2449992717</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4677-d110b3ccdeb1098b6065a9272eb95d6ed75e35c056cd8fee60f4d0661bd437553</originalsourceid><addsrcrecordid>eNqFkb1PwzAQxS0EoqUws6FKLCxp_Z1kQYKqBaRKLDBbjn2hqdKk2E1R_3scUipgwYutu5-f7t1D6JLgEQlnTJgUEeVMjAjjND5C_UPlGPUxlWmUcMl66Mz7JcY4FZSeoh5jmBNORR_Je1jobVE3TpfDHLbghg5sY8APna5Cp60XVQ5mU9RVeA03tbb-HJ3kuvRwsb8H6HU2fZk8RvPnh6fJ3TwyXMZxZAnBGTPGQkZwmmQSS6FTGlPIUmEl2FgAEwYLaWySA0icc4ulJJnlLBaCDdBtp7tushVYA9UmDKTWrlhpt1O1LtTvTlUs1Fu9VbEItnESBG72Aq5-b8Bv1KrwBspSV1A3XlHO0zRMROKAXv9Bl2EtVbCnKCOEC5rglhp3lHG19w7ywzAEqzYT1Sag2gTUVybhx9VPDwf-O4QAiA74KErY_aenZtNJJ_wJbrKVlQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2311452807</pqid></control><display><type>article</type><title>Behavioural fever reduces ranaviral infection in toads</title><source>Wiley-Blackwell Read &amp; Publish Collection</source><creator>Sauer, Erin L. ; Trejo, Nadia ; Hoverman, Jason T. ; Rohr, Jason R. ; Pedersen, Amy</creator><contributor>Pedersen, Amy</contributor><creatorcontrib>Sauer, Erin L. ; Trejo, Nadia ; Hoverman, Jason T. ; Rohr, Jason R. ; Pedersen, Amy ; Pedersen, Amy</creatorcontrib><description>Host behaviour is known to influence disease dynamics. Additionally, hosts often change their behaviours in response to pathogen detection to resist and avoid disease. The capacity of wildlife populations to respond to pathogens using behavioural plasticity is critical for reducing the impacts of disease outbreaks. However, there is limited information regarding the ability of ectothermic vertebrates to resist diseases via behavioural plasticity. Here, we experimentally examine the effect of host behaviour on ranaviral infections, which affect at least 175 species of ectothermic vertebrates. We placed metamorphic (temporal block 1) or adult (block 2) southern toads (Anaxyrus terrestris) in thermal gradients, tested their temperature preferences before and after oral inoculation by measuring individual‐level body temperature over time, and measured ranaviral loads of viral‐exposed individuals. We found significant individual‐level variation in temperature preference and evidence for behavioural fever in both metamorphic and adult A. terrestris during the first 2 days after exposure. Additionally, we found that individual‐level change in temperature preference was negatively correlated with ranaviral load and a better predictor of load than average temperature preference or maximum temperature reached by an individual. In other words, an increase in baseline temperature preference was more important than simply reaching an absolute temperature. These results suggest that behavioural fever is an effective mechanism for resisting ranaviral infections. A free Plain Language Summary can be found within the Supporting Information of this article. A free Plain Language Summary can be found within the Supporting Information of this article.</description><identifier>ISSN: 0269-8463</identifier><identifier>EISSN: 1365-2435</identifier><identifier>DOI: 10.1111/1365-2435.13427</identifier><identifier>PMID: 33041425</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>amphibian declines ; Animal behavior ; behavioural fever ; Body temperature ; Disease ; Disease control ; disease ecology ; Fever ; Infections ; Inoculation ; Pathogens ; Plastic properties ; Plasticity ; Preferences ; ranavirus ; Temperature ; Temperature preferences ; thermal biology ; thermoregulation ; Toads ; Vertebrates ; Wildlife</subject><ispartof>Functional ecology, 2019-11, Vol.33 (11), p.2172-2179</ispartof><rights>2019 The Authors. Functional Ecology © 2019 British Ecological Society</rights><rights>Functional Ecology © 2019 British Ecological Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4677-d110b3ccdeb1098b6065a9272eb95d6ed75e35c056cd8fee60f4d0661bd437553</citedby><cites>FETCH-LOGICAL-c4677-d110b3ccdeb1098b6065a9272eb95d6ed75e35c056cd8fee60f4d0661bd437553</cites><orcidid>0000-0002-8339-6498 ; 0000-0002-4002-2728</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33041425$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Pedersen, Amy</contributor><creatorcontrib>Sauer, Erin L.</creatorcontrib><creatorcontrib>Trejo, Nadia</creatorcontrib><creatorcontrib>Hoverman, Jason T.</creatorcontrib><creatorcontrib>Rohr, Jason R.</creatorcontrib><creatorcontrib>Pedersen, Amy</creatorcontrib><title>Behavioural fever reduces ranaviral infection in toads</title><title>Functional ecology</title><addtitle>Funct Ecol</addtitle><description>Host behaviour is known to influence disease dynamics. Additionally, hosts often change their behaviours in response to pathogen detection to resist and avoid disease. The capacity of wildlife populations to respond to pathogens using behavioural plasticity is critical for reducing the impacts of disease outbreaks. However, there is limited information regarding the ability of ectothermic vertebrates to resist diseases via behavioural plasticity. Here, we experimentally examine the effect of host behaviour on ranaviral infections, which affect at least 175 species of ectothermic vertebrates. We placed metamorphic (temporal block 1) or adult (block 2) southern toads (Anaxyrus terrestris) in thermal gradients, tested their temperature preferences before and after oral inoculation by measuring individual‐level body temperature over time, and measured ranaviral loads of viral‐exposed individuals. We found significant individual‐level variation in temperature preference and evidence for behavioural fever in both metamorphic and adult A. terrestris during the first 2 days after exposure. Additionally, we found that individual‐level change in temperature preference was negatively correlated with ranaviral load and a better predictor of load than average temperature preference or maximum temperature reached by an individual. In other words, an increase in baseline temperature preference was more important than simply reaching an absolute temperature. These results suggest that behavioural fever is an effective mechanism for resisting ranaviral infections. A free Plain Language Summary can be found within the Supporting Information of this article. A free Plain Language Summary can be found within the Supporting Information of this article.</description><subject>amphibian declines</subject><subject>Animal behavior</subject><subject>behavioural fever</subject><subject>Body temperature</subject><subject>Disease</subject><subject>Disease control</subject><subject>disease ecology</subject><subject>Fever</subject><subject>Infections</subject><subject>Inoculation</subject><subject>Pathogens</subject><subject>Plastic properties</subject><subject>Plasticity</subject><subject>Preferences</subject><subject>ranavirus</subject><subject>Temperature</subject><subject>Temperature preferences</subject><subject>thermal biology</subject><subject>thermoregulation</subject><subject>Toads</subject><subject>Vertebrates</subject><subject>Wildlife</subject><issn>0269-8463</issn><issn>1365-2435</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkb1PwzAQxS0EoqUws6FKLCxp_Z1kQYKqBaRKLDBbjn2hqdKk2E1R_3scUipgwYutu5-f7t1D6JLgEQlnTJgUEeVMjAjjND5C_UPlGPUxlWmUcMl66Mz7JcY4FZSeoh5jmBNORR_Je1jobVE3TpfDHLbghg5sY8APna5Cp60XVQ5mU9RVeA03tbb-HJ3kuvRwsb8H6HU2fZk8RvPnh6fJ3TwyXMZxZAnBGTPGQkZwmmQSS6FTGlPIUmEl2FgAEwYLaWySA0icc4ulJJnlLBaCDdBtp7tushVYA9UmDKTWrlhpt1O1LtTvTlUs1Fu9VbEItnESBG72Aq5-b8Bv1KrwBspSV1A3XlHO0zRMROKAXv9Bl2EtVbCnKCOEC5rglhp3lHG19w7ywzAEqzYT1Sag2gTUVybhx9VPDwf-O4QAiA74KErY_aenZtNJJ_wJbrKVlQ</recordid><startdate>201911</startdate><enddate>201911</enddate><creator>Sauer, Erin L.</creator><creator>Trejo, Nadia</creator><creator>Hoverman, Jason T.</creator><creator>Rohr, Jason R.</creator><creator>Pedersen, Amy</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7SN</scope><scope>7SS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8339-6498</orcidid><orcidid>https://orcid.org/0000-0002-4002-2728</orcidid></search><sort><creationdate>201911</creationdate><title>Behavioural fever reduces ranaviral infection in toads</title><author>Sauer, Erin L. ; Trejo, Nadia ; Hoverman, Jason T. ; Rohr, Jason R. ; Pedersen, Amy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4677-d110b3ccdeb1098b6065a9272eb95d6ed75e35c056cd8fee60f4d0661bd437553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>amphibian declines</topic><topic>Animal behavior</topic><topic>behavioural fever</topic><topic>Body temperature</topic><topic>Disease</topic><topic>Disease control</topic><topic>disease ecology</topic><topic>Fever</topic><topic>Infections</topic><topic>Inoculation</topic><topic>Pathogens</topic><topic>Plastic properties</topic><topic>Plasticity</topic><topic>Preferences</topic><topic>ranavirus</topic><topic>Temperature</topic><topic>Temperature preferences</topic><topic>thermal biology</topic><topic>thermoregulation</topic><topic>Toads</topic><topic>Vertebrates</topic><topic>Wildlife</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sauer, Erin L.</creatorcontrib><creatorcontrib>Trejo, Nadia</creatorcontrib><creatorcontrib>Hoverman, Jason T.</creatorcontrib><creatorcontrib>Rohr, Jason R.</creatorcontrib><creatorcontrib>Pedersen, Amy</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Functional ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sauer, Erin L.</au><au>Trejo, Nadia</au><au>Hoverman, Jason T.</au><au>Rohr, Jason R.</au><au>Pedersen, Amy</au><au>Pedersen, Amy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Behavioural fever reduces ranaviral infection in toads</atitle><jtitle>Functional ecology</jtitle><addtitle>Funct Ecol</addtitle><date>2019-11</date><risdate>2019</risdate><volume>33</volume><issue>11</issue><spage>2172</spage><epage>2179</epage><pages>2172-2179</pages><issn>0269-8463</issn><eissn>1365-2435</eissn><abstract>Host behaviour is known to influence disease dynamics. Additionally, hosts often change their behaviours in response to pathogen detection to resist and avoid disease. The capacity of wildlife populations to respond to pathogens using behavioural plasticity is critical for reducing the impacts of disease outbreaks. However, there is limited information regarding the ability of ectothermic vertebrates to resist diseases via behavioural plasticity. Here, we experimentally examine the effect of host behaviour on ranaviral infections, which affect at least 175 species of ectothermic vertebrates. We placed metamorphic (temporal block 1) or adult (block 2) southern toads (Anaxyrus terrestris) in thermal gradients, tested their temperature preferences before and after oral inoculation by measuring individual‐level body temperature over time, and measured ranaviral loads of viral‐exposed individuals. We found significant individual‐level variation in temperature preference and evidence for behavioural fever in both metamorphic and adult A. terrestris during the first 2 days after exposure. Additionally, we found that individual‐level change in temperature preference was negatively correlated with ranaviral load and a better predictor of load than average temperature preference or maximum temperature reached by an individual. In other words, an increase in baseline temperature preference was more important than simply reaching an absolute temperature. These results suggest that behavioural fever is an effective mechanism for resisting ranaviral infections. A free Plain Language Summary can be found within the Supporting Information of this article. A free Plain Language Summary can be found within the Supporting Information of this article.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33041425</pmid><doi>10.1111/1365-2435.13427</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-8339-6498</orcidid><orcidid>https://orcid.org/0000-0002-4002-2728</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0269-8463
ispartof Functional ecology, 2019-11, Vol.33 (11), p.2172-2179
issn 0269-8463
1365-2435
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7546308
source Wiley-Blackwell Read & Publish Collection
subjects amphibian declines
Animal behavior
behavioural fever
Body temperature
Disease
Disease control
disease ecology
Fever
Infections
Inoculation
Pathogens
Plastic properties
Plasticity
Preferences
ranavirus
Temperature
Temperature preferences
thermal biology
thermoregulation
Toads
Vertebrates
Wildlife
title Behavioural fever reduces ranaviral infection in toads
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T05%3A16%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Behavioural%20fever%20reduces%20ranaviral%20infection%20in%20toads&rft.jtitle=Functional%20ecology&rft.au=Sauer,%20Erin%20L.&rft.date=2019-11&rft.volume=33&rft.issue=11&rft.spage=2172&rft.epage=2179&rft.pages=2172-2179&rft.issn=0269-8463&rft.eissn=1365-2435&rft_id=info:doi/10.1111/1365-2435.13427&rft_dat=%3Cproquest_pubme%3E2449992717%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4677-d110b3ccdeb1098b6065a9272eb95d6ed75e35c056cd8fee60f4d0661bd437553%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2311452807&rft_id=info:pmid/33041425&rfr_iscdi=true