Can the behaviour of threespine stickleback parasitized with Schistocephalus solidus be replicated by manipulating host physiology?
Sticklebacks infected by the parasitic flatworm Schistocephalus solidus show dramatic changes in phenotype, including a loss of species-typical behavioural responses to predators. The timing of host behaviour change coincides with the development of infectivity of the parasite to the final host (a p...
Gespeichert in:
Veröffentlicht in: | Journal of experimental biology 2017-01, Vol.220 (Pt 2), p.237-246 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 246 |
---|---|
container_issue | Pt 2 |
container_start_page | 237 |
container_title | Journal of experimental biology |
container_volume | 220 |
creator | Grécias, Lucie Hébert, François Olivier Berger, Chloé Suzanne Barber, Iain Aubin-Horth, Nadia |
description | Sticklebacks infected by the parasitic flatworm Schistocephalus solidus show dramatic changes in phenotype, including a loss of species-typical behavioural responses to predators. The timing of host behaviour change coincides with the development of infectivity of the parasite to the final host (a piscivorous bird), making it an ideal model for studying the mechanisms of infection-induced behavioural modification. However, whether the loss of host anti-predator behaviour results from direct manipulation by the parasite, or is a by-product (e.g. host immune response) or side effect of infection (e.g. energetic loss), remains controversial. To understand the physiological mechanisms that generate these behavioural changes, we quantified the behavioural profiles of experimentally infected fish and attempted to replicate these in non-parasitized fish by exposing them to treatments including immunity activation and fasting, or by pharmacologically inhibiting the stress axis. All fish were screened for the following behaviours: activity, water depth preference, sociability, phototaxis, anti-predator response and latency to feed. We were able to change individual behaviours with certain treatments. Our results suggest that the impact of S. solidus on the stickleback might be of a multifactorial nature. The behaviour changes observed in infected fish might result from the combined effects of modifying the serotonergic axis, lack of energy and activation of the immune system. |
doi_str_mv | 10.1242/jeb.151456 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1872822240</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1872822240</sourcerecordid><originalsourceid>FETCH-LOGICAL-c348t-5ff40b7c69b8334edf75413e0959259ed59a1366c90d3dc1659eb46620e5a8ef3</originalsourceid><addsrcrecordid>eNqNkc1rFTEUxYMo9rW68Q-QgBspTM33TFZSHn5BoYvqekgydzp5zZuMSUZ5bvuPN_KqC1fezeEefhy49yD0ipILygR7twN7QSUVUj1BGyrattF1eYo2hDDWEC30CTrNeUfqKCmeoxPWdpQyLTbofmtmXCbAFibzw8c14ThWIwHkxc-Ac_HuLoA17g4vJpnsi_8FA_7py4Rv3ORziQ6WyYQ14xyDH6pawAmW4J0pFbUHvDezX9Zgip9v8RRzwct0yD6GeHt4_wI9G03I8PJRz9C3jx--bj83V9efvmwvrxrHRVcaOY6C2NYpbTvOBQxjKwXlQLTUTGoYpDaUK-U0GfjgqKqeFUoxAtJ0MPIz9PaYu6T4fYVc-r3PDkIwM8Q197RrWccYE-Q_UK5aTqXgFX3zD7qrX5zrIT2r_-66thOiUudHyqWYc4KxX5Lfm3ToKel_t9jXFvtjixV-_Ri52j0Mf9E_tfEHFkuZUA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2006887844</pqid></control><display><type>article</type><title>Can the behaviour of threespine stickleback parasitized with Schistocephalus solidus be replicated by manipulating host physiology?</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><source>Company of Biologists</source><creator>Grécias, Lucie ; Hébert, François Olivier ; Berger, Chloé Suzanne ; Barber, Iain ; Aubin-Horth, Nadia</creator><creatorcontrib>Grécias, Lucie ; Hébert, François Olivier ; Berger, Chloé Suzanne ; Barber, Iain ; Aubin-Horth, Nadia</creatorcontrib><description>Sticklebacks infected by the parasitic flatworm Schistocephalus solidus show dramatic changes in phenotype, including a loss of species-typical behavioural responses to predators. The timing of host behaviour change coincides with the development of infectivity of the parasite to the final host (a piscivorous bird), making it an ideal model for studying the mechanisms of infection-induced behavioural modification. However, whether the loss of host anti-predator behaviour results from direct manipulation by the parasite, or is a by-product (e.g. host immune response) or side effect of infection (e.g. energetic loss), remains controversial. To understand the physiological mechanisms that generate these behavioural changes, we quantified the behavioural profiles of experimentally infected fish and attempted to replicate these in non-parasitized fish by exposing them to treatments including immunity activation and fasting, or by pharmacologically inhibiting the stress axis. All fish were screened for the following behaviours: activity, water depth preference, sociability, phototaxis, anti-predator response and latency to feed. We were able to change individual behaviours with certain treatments. Our results suggest that the impact of S. solidus on the stickleback might be of a multifactorial nature. The behaviour changes observed in infected fish might result from the combined effects of modifying the serotonergic axis, lack of energy and activation of the immune system.</description><identifier>ISSN: 0022-0949</identifier><identifier>EISSN: 1477-9145</identifier><identifier>DOI: 10.1242/jeb.151456</identifier><identifier>PMID: 27811294</identifier><language>eng</language><publisher>England: The Company of Biologists Ltd</publisher><subject>Animals ; Behavior ; Behavior, Animal - physiology ; Cestoda - physiology ; Cestode Infections - parasitology ; Cestode Infections - veterinary ; Female ; Fish ; Fish Diseases - parasitology ; Gasterosteus aculeatus ; Host-Parasite Interactions ; Immune response ; Immune system ; Immunity ; Infections ; Infectivity ; Latency ; Male ; Pharmacology ; Phenotypes ; Phototaxis ; Predators ; Schistocephalus solidus ; Smegmamorpha - immunology ; Smegmamorpha - physiology ; Water depth</subject><ispartof>Journal of experimental biology, 2017-01, Vol.220 (Pt 2), p.237-246</ispartof><rights>2017. Published by The Company of Biologists Ltd.</rights><rights>Copyright The Company of Biologists Ltd Jan 15, 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c348t-5ff40b7c69b8334edf75413e0959259ed59a1366c90d3dc1659eb46620e5a8ef3</citedby><cites>FETCH-LOGICAL-c348t-5ff40b7c69b8334edf75413e0959259ed59a1366c90d3dc1659eb46620e5a8ef3</cites><orcidid>0000-0002-9030-634X ; 0000-0003-3955-6674</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3665,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27811294$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Grécias, Lucie</creatorcontrib><creatorcontrib>Hébert, François Olivier</creatorcontrib><creatorcontrib>Berger, Chloé Suzanne</creatorcontrib><creatorcontrib>Barber, Iain</creatorcontrib><creatorcontrib>Aubin-Horth, Nadia</creatorcontrib><title>Can the behaviour of threespine stickleback parasitized with Schistocephalus solidus be replicated by manipulating host physiology?</title><title>Journal of experimental biology</title><addtitle>J Exp Biol</addtitle><description>Sticklebacks infected by the parasitic flatworm Schistocephalus solidus show dramatic changes in phenotype, including a loss of species-typical behavioural responses to predators. The timing of host behaviour change coincides with the development of infectivity of the parasite to the final host (a piscivorous bird), making it an ideal model for studying the mechanisms of infection-induced behavioural modification. However, whether the loss of host anti-predator behaviour results from direct manipulation by the parasite, or is a by-product (e.g. host immune response) or side effect of infection (e.g. energetic loss), remains controversial. To understand the physiological mechanisms that generate these behavioural changes, we quantified the behavioural profiles of experimentally infected fish and attempted to replicate these in non-parasitized fish by exposing them to treatments including immunity activation and fasting, or by pharmacologically inhibiting the stress axis. All fish were screened for the following behaviours: activity, water depth preference, sociability, phototaxis, anti-predator response and latency to feed. We were able to change individual behaviours with certain treatments. Our results suggest that the impact of S. solidus on the stickleback might be of a multifactorial nature. The behaviour changes observed in infected fish might result from the combined effects of modifying the serotonergic axis, lack of energy and activation of the immune system.</description><subject>Animals</subject><subject>Behavior</subject><subject>Behavior, Animal - physiology</subject><subject>Cestoda - physiology</subject><subject>Cestode Infections - parasitology</subject><subject>Cestode Infections - veterinary</subject><subject>Female</subject><subject>Fish</subject><subject>Fish Diseases - parasitology</subject><subject>Gasterosteus aculeatus</subject><subject>Host-Parasite Interactions</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Immunity</subject><subject>Infections</subject><subject>Infectivity</subject><subject>Latency</subject><subject>Male</subject><subject>Pharmacology</subject><subject>Phenotypes</subject><subject>Phototaxis</subject><subject>Predators</subject><subject>Schistocephalus solidus</subject><subject>Smegmamorpha - immunology</subject><subject>Smegmamorpha - physiology</subject><subject>Water depth</subject><issn>0022-0949</issn><issn>1477-9145</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1rFTEUxYMo9rW68Q-QgBspTM33TFZSHn5BoYvqekgydzp5zZuMSUZ5bvuPN_KqC1fezeEefhy49yD0ipILygR7twN7QSUVUj1BGyrattF1eYo2hDDWEC30CTrNeUfqKCmeoxPWdpQyLTbofmtmXCbAFibzw8c14ThWIwHkxc-Ac_HuLoA17g4vJpnsi_8FA_7py4Rv3ORziQ6WyYQ14xyDH6pawAmW4J0pFbUHvDezX9Zgip9v8RRzwct0yD6GeHt4_wI9G03I8PJRz9C3jx--bj83V9efvmwvrxrHRVcaOY6C2NYpbTvOBQxjKwXlQLTUTGoYpDaUK-U0GfjgqKqeFUoxAtJ0MPIz9PaYu6T4fYVc-r3PDkIwM8Q197RrWccYE-Q_UK5aTqXgFX3zD7qrX5zrIT2r_-66thOiUudHyqWYc4KxX5Lfm3ToKel_t9jXFvtjixV-_Ri52j0Mf9E_tfEHFkuZUA</recordid><startdate>20170115</startdate><enddate>20170115</enddate><creator>Grécias, Lucie</creator><creator>Hébert, François Olivier</creator><creator>Berger, Chloé Suzanne</creator><creator>Barber, Iain</creator><creator>Aubin-Horth, Nadia</creator><general>The Company of Biologists Ltd</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>7QP</scope><scope>7QR</scope><scope>7SS</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9030-634X</orcidid><orcidid>https://orcid.org/0000-0003-3955-6674</orcidid></search><sort><creationdate>20170115</creationdate><title>Can the behaviour of threespine stickleback parasitized with Schistocephalus solidus be replicated by manipulating host physiology?</title><author>Grécias, Lucie ; Hébert, François Olivier ; Berger, Chloé Suzanne ; Barber, Iain ; Aubin-Horth, Nadia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c348t-5ff40b7c69b8334edf75413e0959259ed59a1366c90d3dc1659eb46620e5a8ef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Behavior</topic><topic>Behavior, Animal - physiology</topic><topic>Cestoda - physiology</topic><topic>Cestode Infections - parasitology</topic><topic>Cestode Infections - veterinary</topic><topic>Female</topic><topic>Fish</topic><topic>Fish Diseases - parasitology</topic><topic>Gasterosteus aculeatus</topic><topic>Host-Parasite Interactions</topic><topic>Immune response</topic><topic>Immune system</topic><topic>Immunity</topic><topic>Infections</topic><topic>Infectivity</topic><topic>Latency</topic><topic>Male</topic><topic>Pharmacology</topic><topic>Phenotypes</topic><topic>Phototaxis</topic><topic>Predators</topic><topic>Schistocephalus solidus</topic><topic>Smegmamorpha - immunology</topic><topic>Smegmamorpha - physiology</topic><topic>Water depth</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grécias, Lucie</creatorcontrib><creatorcontrib>Hébert, François Olivier</creatorcontrib><creatorcontrib>Berger, Chloé Suzanne</creatorcontrib><creatorcontrib>Barber, Iain</creatorcontrib><creatorcontrib>Aubin-Horth, Nadia</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>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology 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>MEDLINE - Academic</collection><jtitle>Journal of experimental biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grécias, Lucie</au><au>Hébert, François Olivier</au><au>Berger, Chloé Suzanne</au><au>Barber, Iain</au><au>Aubin-Horth, Nadia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Can the behaviour of threespine stickleback parasitized with Schistocephalus solidus be replicated by manipulating host physiology?</atitle><jtitle>Journal of experimental biology</jtitle><addtitle>J Exp Biol</addtitle><date>2017-01-15</date><risdate>2017</risdate><volume>220</volume><issue>Pt 2</issue><spage>237</spage><epage>246</epage><pages>237-246</pages><issn>0022-0949</issn><eissn>1477-9145</eissn><abstract>Sticklebacks infected by the parasitic flatworm Schistocephalus solidus show dramatic changes in phenotype, including a loss of species-typical behavioural responses to predators. The timing of host behaviour change coincides with the development of infectivity of the parasite to the final host (a piscivorous bird), making it an ideal model for studying the mechanisms of infection-induced behavioural modification. However, whether the loss of host anti-predator behaviour results from direct manipulation by the parasite, or is a by-product (e.g. host immune response) or side effect of infection (e.g. energetic loss), remains controversial. To understand the physiological mechanisms that generate these behavioural changes, we quantified the behavioural profiles of experimentally infected fish and attempted to replicate these in non-parasitized fish by exposing them to treatments including immunity activation and fasting, or by pharmacologically inhibiting the stress axis. All fish were screened for the following behaviours: activity, water depth preference, sociability, phototaxis, anti-predator response and latency to feed. We were able to change individual behaviours with certain treatments. Our results suggest that the impact of S. solidus on the stickleback might be of a multifactorial nature. The behaviour changes observed in infected fish might result from the combined effects of modifying the serotonergic axis, lack of energy and activation of the immune system.</abstract><cop>England</cop><pub>The Company of Biologists Ltd</pub><pmid>27811294</pmid><doi>10.1242/jeb.151456</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-9030-634X</orcidid><orcidid>https://orcid.org/0000-0003-3955-6674</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-0949 |
ispartof | Journal of experimental biology, 2017-01, Vol.220 (Pt 2), p.237-246 |
issn | 0022-0949 1477-9145 |
language | eng |
recordid | cdi_proquest_miscellaneous_1872822240 |
source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection; Company of Biologists |
subjects | Animals Behavior Behavior, Animal - physiology Cestoda - physiology Cestode Infections - parasitology Cestode Infections - veterinary Female Fish Fish Diseases - parasitology Gasterosteus aculeatus Host-Parasite Interactions Immune response Immune system Immunity Infections Infectivity Latency Male Pharmacology Phenotypes Phototaxis Predators Schistocephalus solidus Smegmamorpha - immunology Smegmamorpha - physiology Water depth |
title | Can the behaviour of threespine stickleback parasitized with Schistocephalus solidus be replicated by manipulating host physiology? |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T15%3A40%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Can%20the%20behaviour%20of%20threespine%20stickleback%20parasitized%20with%20Schistocephalus%20solidus%20be%20replicated%20by%20manipulating%20host%20physiology?&rft.jtitle=Journal%20of%20experimental%20biology&rft.au=Gr%C3%A9cias,%20Lucie&rft.date=2017-01-15&rft.volume=220&rft.issue=Pt%202&rft.spage=237&rft.epage=246&rft.pages=237-246&rft.issn=0022-0949&rft.eissn=1477-9145&rft_id=info:doi/10.1242/jeb.151456&rft_dat=%3Cproquest_cross%3E1872822240%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2006887844&rft_id=info:pmid/27811294&rfr_iscdi=true |