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dc.contributor.authorCHICO GRAS, VERONICA-
dc.contributor.authorSalvador Mira, Maria Elizabhet-
dc.contributor.authorNombela, Ivan-
dc.contributor.authorPuente Marin, Sara-
dc.contributor.authorCiordia, Sergio-
dc.contributor.authorMena, María Carmen-
dc.contributor.authorPerez, Luis-
dc.contributor.authorcoll, julio-
dc.contributor.authorGuzman, Fanny-
dc.contributor.authorEncinar, José Antonio-
dc.contributor.authorMercado, Luis-
dc.contributor.authorOrtega-Villaizan, Maria del Mar-
dc.date.accessioned2025-01-14T13:05:33Z-
dc.date.available2025-01-14T13:05:33Z-
dc.date.created2017-04-
dc.identifier.citationFrontiers in Immunology, April 2019 | Volume 10es_ES
dc.identifier.issn1664-3224-
dc.identifier.urihttps://hdl.handle.net/11000/34453-
dc.description.abstractViral hemorrhagic septicemia virus (VHSV) infection appears to be halted in rainbow trout nucleated red blood cells (RBCs). Diverse mechanisms are thought to be related to the antiviral immune response of rainbow trout RBCs to VHSV. However, the specific rainbow trout RBC proteins that interact directly with VHSV are still unknown. In an attempt to identify VHSV-RBC protein interactions, we characterized the immunoprecipitated (IP) proteome of RBCs exposed to VHSV using an antibody against the N protein of VHSV. The IP proteomic characterization identified 31 proteins by mass spectrometry analysis. Among them, we identified interferon-induced protein with tetratricopeptide repeats 5 (IFIT5), a protein belonging to a family of proteins that are induced after the production of type I interferon. Importantly, IFIT5 has been implicated in the antiviral immune response. We confirmed the participation of IFIT5 in the rainbow trout RBC antiviral response by examining the expression profile of IFIT5 in RBCs after VHSV exposure at transcriptional and protein levels. We detected a correlation between the highest IFIT5 expression levels and the decline in VHSV replication at 6h post-exposure. In addition, silencing ifit5 resulted in a significant increase in VHSV replication in RBCs. Moreover, an increase in VHSV replication was observed in RBCs when the IFIT5 RNA-binding pocket cavity was modulated by using a natural compound from the SuperNatural II database. We performed a proximity ligation assay and detected a significant increase in positive cells among VHSV-exposed RBCs compared to unexposed RBCs, indicating protein-protein colocalization between IFIT5 and the glycoprotein G of VHSV. In summary, thees_ES
dc.formatapplication/pdfes_ES
dc.format.extent15es_ES
dc.language.isoenges_ES
dc.publisherFrontiers Mediaes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectrainbowtroutes_ES
dc.subjectIFIT5es_ES
dc.subjectredbloodcellses_ES
dc.subjecterythrocytees_ES
dc.subjectVHSVes_ES
dc.subjectantiviral immune responsees_ES
dc.subjectimmunoprecipitatees_ES
dc.subjectproteomices_ES
dc.subject.otherCDU::6 - Ciencias aplicadas::60 - Cuestiones generales de las ciencias aplicadases_ES
dc.titleIFIT5 Participates in the Antiviral Mechanisms of Rainbow Trout Red Blood Cellses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.contributor.instituteInstitutos de la UMH::Instituto de Investigación, Desarrollo e Innovación en Biotecnología Sanitaria de Elchees_ES
dc.relation.publisherversionhttps://doi.org/10.3389/fimmu.2019.00613es_ES
Aparece en las colecciones:
Instituto de Investigación, Desarrollo e Innovación en Biotecnología Sanitaria de Elche


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