Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/21411
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dc.contributor.authorGarcia-Valtanen, Pabloen_UK
dc.contributor.authorOrtega-Villaizan, Maria del Maren_UK
dc.contributor.authorMartinez-Lopez, Aliciaen_UK
dc.contributor.authorMedina-Gali, Reglaen_UK
dc.contributor.authorPerez, Luisen_UK
dc.contributor.authorMacKenzie, Simonen_UK
dc.contributor.authorFigueras, Antonioen_UK
dc.contributor.authorColl, Julio Men_UK
dc.contributor.authorEstepa, Amparoen_UK
dc.date.accessioned2015-07-23T08:24:13Z-
dc.date.available2015-07-23T08:24:13Z-
dc.date.issued2014-09en_UK
dc.identifier.urihttp://hdl.handle.net/1893/21411-
dc.description.abstractIt has not been elucidated whether or not autophagy is induced by rhabdoviral G glycoproteins (G) in vertebrate organisms for which rhabdovirus infection is lethal. Our work provides the first evidence that both mammalian (vesicular stomatitis virus, VSV) and fish (viral hemorrhagic septicemia virus, VHSV, and spring viremia carp virus, SVCV) rhabdoviral Gs induce an autophagic antiviral program in vertebrate cell lines. The transcriptomic profiles obtained from zebrafish genetically immunized with either Gsvcv or Gvhsv suggest that autophagy is induced shortly after immunization and therefore, it may be an important component of the strong antiviral immune responses elicited by these viral proteins. Pepscan mapping of autophagy-inducing linear determinants of Gvhsv and Gvsv showed that peptides located in their fusion domains induce autophagy. Altogether these results suggest that strategies aimed at modulating autophagy could be used for the prevention and treatment of rhabdoviral infections such as rabies, which causes thousands of human deaths every year.en_UK
dc.language.isoenen_UK
dc.publisherTaylor and Francisen_UK
dc.relationGarcia-Valtanen P, Ortega-Villaizan MdM, Martinez-Lopez A, Medina-Gali R, Perez L, MacKenzie S, Figueras A, Coll JM & Estepa A (2014) Autophagy-inducing peptides from mammalian VSV and fish VHSV rhabdoviral G glycoproteins (G) as models for the development of new therapeutic molecules. Autophagy, 10 (9), pp. 1666-1680. https://doi.org/10.4161/auto.29557en_UK
dc.rightsCopyright © 2014 Landes Bioscience This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. Permission is granted subject to the terms of the License under which the work was published. Please check the License conditions for the work which you wish to reuse. Full and appropriate attribution must be given. This permission does not cover any third party copyrighted material which may appear in the work requested.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/en_UK
dc.subjectantiviralen_UK
dc.subjectautophagyen_UK
dc.subjectimmune responseen_UK
dc.subjectLC3en_UK
dc.subjectmicroarraysen_UK
dc.subjectpepscanen_UK
dc.subjectrhabdovirusen_UK
dc.subjectSVCVen_UK
dc.subjectVHSVen_UK
dc.subjectviral glycoproteinen_UK
dc.subjectVSVen_UK
dc.subjectzebrafishen_UK
dc.titleAutophagy-inducing peptides from mammalian VSV and fish VHSV rhabdoviral G glycoproteins (G) as models for the development of new therapeutic moleculesen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.4161/auto.29557en_UK
dc.citation.jtitleAutophagyen_UK
dc.citation.issn1554-8635en_UK
dc.citation.issn1554-8627en_UK
dc.citation.volume10en_UK
dc.citation.issue9en_UK
dc.citation.spage1666en_UK
dc.citation.epage1680en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.author.emailsimon.mackenzie@stir.ac.uken_UK
dc.contributor.affiliationThe Miguel Hernandez University of Elcheen_UK
dc.contributor.affiliationThe Miguel Hernandez University of Elcheen_UK
dc.contributor.affiliationThe Miguel Hernandez University of Elcheen_UK
dc.contributor.affiliationLabiofamen_UK
dc.contributor.affiliationThe Miguel Hernandez University of Elcheen_UK
dc.contributor.affiliationComplex Systems - LEGACYen_UK
dc.contributor.affiliationSpanish National Research Council (CSIC)en_UK
dc.contributor.affiliationINIA-SIGT–Biotecnologiaen_UK
dc.contributor.affiliationThe Miguel Hernandez University of Elcheen_UK
dc.identifier.isiWOS:000341647200015en_UK
dc.identifier.scopusid2-s2.0-84907170731en_UK
dc.identifier.wtid605745en_UK
dc.contributor.orcid0000-0003-1845-6826en_UK
dc.date.accepted2014-06-11en_UK
dcterms.dateAccepted2014-06-11en_UK
dc.date.filedepositdate2015-01-28en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorGarcia-Valtanen, Pablo|en_UK
local.rioxx.authorOrtega-Villaizan, Maria del Mar|en_UK
local.rioxx.authorMartinez-Lopez, Alicia|en_UK
local.rioxx.authorMedina-Gali, Regla|en_UK
local.rioxx.authorPerez, Luis|en_UK
local.rioxx.authorMacKenzie, Simon|0000-0003-1845-6826en_UK
local.rioxx.authorFigueras, Antonio|en_UK
local.rioxx.authorColl, Julio M|en_UK
local.rioxx.authorEstepa, Amparo|en_UK
local.rioxx.projectInternal Project|University of Stirling|https://isni.org/isni/0000000122484331en_UK
local.rioxx.freetoreaddate2015-01-28en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by-nc/4.0/|2015-01-28|en_UK
local.rioxx.filenameMacKenzie_Autophagy 2014.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source1554-8627en_UK
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