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Transcriptome analysis of rainbow trout in response to non-virion (NV) protein of Viral Haemorrhagic Septicaemia virus (VHSV)

dc.contributor.authorChinchilla Rodríguez, Blanca
dc.contributor.authorEncinas, Paloma
dc.contributor.authorEstepa, Amparo
dc.contributor.authorColl Morales, Julio
dc.contributor.authorGómez Casado, Eduardo
dc.date.accessioned2024-01-31T17:04:08Z
dc.date.available2024-01-31T17:04:08Z
dc.date.issued2015
dc.descriptionBlanca Chinchilla is a research fellow FPI (2012) of the Ministerio of the Ministry of Economy and Competitiveness of Spain.
dc.description.abstractThe non-virion (NV) protein of viral haemorrhagic septicaemia virus (VHSV), an economically important fish novirhabdovirus, has been implicated in the interference of some host innate mechanisms (i.e. apoptosis) in vitro. This work aimed to characterise the immune-related transcriptome changes in rainbow trout induced by NV protein that have not yet been established in vivo. For that purpose, immune-targeted microarrays were used to analyse the transcriptomes from head kidney and spleen of rainbow trout (Oncorhynchus mykiss) after injection of recombinant NV (rNV). Results showed the extensive downregulation (and in some cases upregulation) of many innate and adaptive immune response genes not related previously to VHSV infection. The newly identified genes belonged to VHSV-induced genes (vigs), tumour necrosis factors, Toll-like receptors, antigen processing and presentation, immune co-stimulatory molecules, interleukins, macrophage chemotaxis, transcription factors, etc. Classification of differentially downregulated genes into rainbow trout immune pathways identified stat1 and jun/atf1 transcription factor genes as the most representative of the multipath gene targets of rNV. Altogether, these results contribute to define the role and effects of NV in trout by orchestrating an immunosuppression of the innate immune responses for favouring viral replication upon VHSV infection. Finally, these transcriptome results open up the possibility to find out new strategies against VHSV and better understand the interrelationships between some immune pathways in trout.
dc.description.departmentDepto. de Producción Animal
dc.description.facultyFac. de Veterinaria
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Economía y Competitividad (España)
dc.description.statuspub
dc.identifier.citationChinchilla, B., Encinas, P., Estepa, A., Coll, J. M., & Gomez-Casado, E. (2015). Transcriptome analysis of rainbow trout in response to non-virion (NV) protein of viral haemorrhagic septicaemia virus (VHSV). Applied microbiology and biotechnology, 99(4), 1827–1843. https://doi.org/10.1007/s00253-014-6366-3
dc.identifier.doi10.1007/s00253-014-6366-3
dc.identifier.essn1432-0614
dc.identifier.issn0175-7598
dc.identifier.officialurlhttps://doi.org/10.1007/s00253-014-6366-3
dc.identifier.pmid25592735
dc.identifier.urihttps://hdl.handle.net/20.500.14352/97345
dc.issue.number4
dc.journal.titleApplied Microbiology and Biotechnology
dc.language.isoeng
dc.page.final1843
dc.page.initial1827
dc.publisherSpringerLink
dc.relation.projectIDThis work was supported by the projects INGENIO2010 CONSOLIDER 2007-00002, AGL2011-28921-CO3-02 and AGL2014-51773-C3-3 of the Ministry of Economy and Competitiveness of Spain.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsrestricted access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.keywordNovirhabdoviruses
dc.subject.keywordVHSV
dc.subject.keywordNV
dc.subject.keywordTranscriptome
dc.subject.keywordRainbow trout
dc.subject.keywordTargeted-microarrays
dc.subject.keywordVHSV-induced genes (VIG)
dc.subject.ucmVeterinaria
dc.subject.unesco24 Ciencias de la Vida
dc.titleTranscriptome analysis of rainbow trout in response to non-virion (NV) protein of Viral Haemorrhagic Septicaemia virus (VHSV)
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number99
dspace.entity.typePublication
relation.isAuthorOfPublicationfe7e9301-87c6-4efc-a427-a0610189c663
relation.isAuthorOfPublication.latestForDiscoveryfe7e9301-87c6-4efc-a427-a0610189c663

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