Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/47250
DC FieldValueLanguage
dc.contributor.authorAcosta, F.
dc.contributor.authorCollet, B.
dc.contributor.authorLorenzen, N.
dc.contributor.authorEllis, A. E.
dc.date.accessioned2018-11-23T12:02:13Z-
dc.date.available2018-11-23T12:02:13Z-
dc.date.issued2006
dc.identifier.issn1050-4648
dc.identifier.urihttp://hdl.handle.net/10553/47250-
dc.description.abstractIn the present study using a luciferase/Mx promoter reporter system, it was shown that the rainbow trout gonad cell line (RTG-P1), a fibroblastic cell line, produces IFN when transfected with a plasmid encoding the glycoprotein of VHSV but not with plasmid vector alone. Only a small percentage of the cells expressed the G protein on the surface membrane as indicated by immunostaining of transfected cells. When transfection was performed in the presence of monoclonal antibodies (Mab) to the glycoprotein, the production of interferon mRNA transcripts was reduced by over 50%. This indicates that the surface expression of G protein was the major mechanism of interferon induction and that most of the interferon was being expressed by cells neighbouring the transfected cells. Crown Copyright (c) 2006 Published by Elsevier Ltd. All rights reserved.
dc.publisher1050-4648
dc.relation.ispartofFish and Shellfish Immunology
dc.sourceFish and Shellfish Immunology[ISSN 1050-4648],v. 21, p. 272-278
dc.subject.otherRainbow-Trout
dc.subject.otherMonoclonal-Antibodies
dc.subject.otherDna Vaccination
dc.subject.otherEgtved Virus
dc.subject.otherProtective Immunity
dc.subject.otherAlpha-Interferon
dc.subject.otherI Interferon
dc.subject.otherCoronavirus
dc.subject.otherInduction
dc.subject.otherVaccines
dc.titleExpression of the glycoprotein of viral haemorrhagic septicaemia virus (VHSV) on the surface of the fish cell line RTG-P1 induces type 1 interferon expression in neighbouring cells
dc.typeinfo:eu-repo/semantics/Articlees
dc.typeArticlees
dc.identifier.doi10.1016/j.fsi.2005.12.006
dc.identifier.scopus33646788099-
dc.identifier.isi000238497900006
dc.contributor.authorscopusid56269311600
dc.contributor.authorscopusid7005507303
dc.contributor.authorscopusid7003735135
dc.contributor.authorscopusid7201547148
dc.description.lastpage278
dc.description.firstpage272
dc.relation.volume21
dc.type2Artículoes
dc.contributor.daisngid878226
dc.contributor.daisngid264674
dc.contributor.daisngid402283
dc.contributor.daisngid196213
dc.contributor.wosstandardWOS:Acosta, F
dc.contributor.wosstandardWOS:Collet, B
dc.contributor.wosstandardWOS:Lorenzen, N
dc.contributor.wosstandardWOS:Ellis, AE
dc.date.coverdateEnero 2006
dc.identifier.ulpgces
dc.description.jcr2,725
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.orcid0000-0002-1098-7529-
crisitem.author.parentorgIU de Investigación en Acuicultura Sostenible y Ec-
crisitem.author.fullNameAcosta Arbelo, Félix Antonio-
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