Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/47249
DC FieldValueLanguage
dc.contributor.authorCollet, Bertrand-
dc.contributor.authorMunro, Eann S.-
dc.contributor.authorGahlawat, Suresh-
dc.contributor.authorAcosta, Felix-
dc.contributor.authorGarcia, Jose-
dc.contributor.authorRoemelt, Christina-
dc.contributor.authorZou, Jun-
dc.contributor.authorSecombes, Christopher J.-
dc.contributor.authorEllis, Anthony E.-
dc.date.accessioned2018-11-23T12:01:44Z-
dc.date.available2018-11-23T12:01:44Z-
dc.date.issued2007-
dc.identifier.issn1050-4648-
dc.identifier.urihttp://hdl.handle.net/10553/47249-
dc.description.abstractRTG-P1 cells are a rainbow trout fibroblastic cell line permanently transfected with the luciferase gene under the control of the Mx promoter. On exposure to interferon (IFN) or IFN inducing agents, the cells produce luciferase. IPNV did not induce luciferase production up to 24 h post-infection but did not suppress constitutive luciferase production. Furthermore, IPNV suppressed luciferase production induced by poly I:C. RT-PCR analysis of IPNV infected cells showed IFN gene transcription from 6 h post-infection with increasing expression up to 24 h. Housekeeping genes beta-actin and GAPDH were also expressed along with upregulation of IRF1 and slight upregulation of STAT1. When RTG-P1 cells were stimulated with IFN, Mx transcripts, measured by qRT-PCR, peaked at 3-6 h and thereafter fell to low levels, but in the presence of IPNV, Mx transcription at this time was significantly suppressed but continued to rise gradually. Luciferase production was lower in infected cells at 12 h post-infection but not significantly after 24 h.These results indicate that, in non-stimulated RTG-P1 cells, while IPNV induces IFN transcription, activation of Mx expression is suppressed. Furthermore, when stimulated by IFN, the rate of Mx transcription is significantly suppressed by the virus. This would probably give time for the virus to replicate rapidly in the early phases of infection.Contrary to the fibroblastic cell line, IPNV stimulated IFN production by salmon macrophages in vitro at least as strongly as poly I:C, with no suppression of the IFN response to poly I:C, and the virus persisted for up to 9 days without causing CPE. (c) 2006 Published by Elsevier Ltd.-
dc.publisher1050-4648-
dc.relation.ispartofFish and Shellfish Immunology-
dc.sourceFish and Shellfish Immunology[ISSN 1050-4648],v. 22, p. 44-56-
dc.subject.otherDouble-Stranded-Rna-
dc.subject.otherMx Messenger-Rna-
dc.subject.otherAntiviral Responses-
dc.subject.otherSalar L.-
dc.subject.otherExpression-
dc.subject.otherProtein-
dc.subject.otherCloning-
dc.subject.otherFamily-
dc.subject.otherFish-
dc.subject.otherInhibition-
dc.titleInfectious pancreatic necrosis virus suppresses type I interferon signalling in rainbow trout gonad cell line but not in Atlantic salmon macrophages-
dc.typeinfo:eu-repo/semantics/Articlees
dc.typeArticlees
dc.identifier.doi10.1016/j.fsi.2006.03.011-
dc.identifier.scopus33750052916-
dc.identifier.isi000241924000005-
dc.contributor.authorscopusid7005507303-
dc.contributor.authorscopusid7006205558-
dc.contributor.authorscopusid6505839479-
dc.contributor.authorscopusid56269311600-
dc.contributor.authorscopusid55619305765-
dc.contributor.authorscopusid57215286511-
dc.contributor.authorscopusid15021379300-
dc.contributor.authorscopusid34574384400-
dc.contributor.authorscopusid7005974493-
dc.contributor.authorscopusid7201547148-
dc.description.lastpage56-
dc.description.firstpage44-
dc.relation.volume22-
dc.type2Artículoes
dc.contributor.daisngid264674-
dc.contributor.daisngid1679883-
dc.contributor.daisngid2302063-
dc.contributor.daisngid1422265-
dc.contributor.daisngid6487659-
dc.contributor.daisngid9530730-
dc.contributor.daisngid431287-
dc.contributor.daisngid34998-
dc.contributor.daisngid1386024-
dc.contributor.wosstandardWOS:Collet, B-
dc.contributor.wosstandardWOS:Munro, ES-
dc.contributor.wosstandardWOS:Gahlawat, S-
dc.contributor.wosstandardWOS:Acosta, F-
dc.contributor.wosstandardWOS:Garcia, J-
dc.contributor.wosstandardWOS:Roemelt, C-
dc.contributor.wosstandardWOS:Zou, J-
dc.contributor.wosstandardWOS:Secombes, CJ-
dc.contributor.wosstandardWOS:Ellis, AE-
dc.date.coverdateEnero 2007-
dc.identifier.ulpgces
dc.description.jcr3,16
dc.description.jcrqQ1
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR Grupo de Investigación en Acuicultura-
crisitem.author.deptIU de Investigación en Acuicultura Sostenible y Ec-
crisitem.author.deptDepartamento de Patología Animal, Producción Animal, Bromatología y Tecnología de Los Alimentos-
crisitem.author.deptGIR IUMA: Sistemas de Información y Comunicaciones-
crisitem.author.deptIU de Microelectrónica Aplicada-
crisitem.author.deptDepartamento de Ingeniería Electrónica y Automática-
crisitem.author.orcid0000-0002-1098-7529-
crisitem.author.orcid0000-0003-3561-0135-
crisitem.author.parentorgIU de Investigación en Acuicultura Sostenible y Ec-
crisitem.author.parentorgIU de Microelectrónica Aplicada-
crisitem.author.fullNameAcosta Arbelo, Félix Antonio-
crisitem.author.fullNameGarcía García, Javier Agustín-
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