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Zebra Fish Lacking Adaptive Immunity Acquire an Antiviral Alert State Characterized by Upregulated Gene Expression of Apoptosis, Multigene Families, and Interferon-Related Genes

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dc.contributor.author García-Valtanen, Pablo
dc.contributor.author Martínez-López, Alicia
dc.contributor.author López-Muñoz, Azucena
dc.contributor.author Bello-Pérez, Melissa
dc.contributor.author Medina-Gali, Regla-M
dc.contributor.author Ortega-Villaizan, María-del-Mar
dc.contributor.author Varela, Mónica
dc.contributor.author Figueras, Antonio
dc.contributor.author Mulero, Victoriano
dc.contributor.author Novoa, Beatriz
dc.contributor.author Estepa, Amparo
dc.contributor.author Coll, Julio
dc.date.accessioned 2026-01-19T16:06:02Z
dc.date.available 2026-01-19T16:06:02Z
dc.date.issued 2017-02-13
dc.identifier.citation García-Valtanen P, Martínez-López A, López-Muñoz A, Bello-Perez M, Medina-Gali RM, Ortega-Villaizán MDM, et al. Zebra Fish Lacking Adaptive Immunity Acquire an Antiviral Alert State Characterized by Upregulated Gene Expression of Apoptosis, Multigene Families, and Interferon-Related Genes. Front Immunol [Internet]. 13 de febrero de 2017 [citado 13 de enero de 2026];8. Disponible en: http://journal.frontiersin.org/article/10.3389/fimmu.2017.00121/full
dc.identifier.issn 1664-3224
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/23742
dc.description.abstract To investigate fish innate immunity, we have conducted organ and cell immune-related transcriptomic as well as immunohistologic analysis in mutant zebra fish (Danio rerio) lacking adaptive immunity (rag1(-/-)) at different developmental stages (egg, larvae, and adult), before and after infection with spring viremia carp virus (SVCV). The results revealed that, compared to immunocompetent zebra fish (rag1(+/+) ), rag1(-/-) acquired increased resistance to SVCV with age, correlating with elevated transcript levels of immune genes in skin/fins and lymphoid organs (head kidney and spleen). Gene sets corresponding to apoptotic functions, immune-related multigene families, and interferon-related genes were constitutively upregulated in uninfected adult rag1(-/-) zebra fish. Overexpression of activated CASPASE-3 in different tissues before and after infection with SVCV further confirmed increased apoptotic function in rag1(-/-) zebra fish. Concurrently, staining of different tissue samples with a pan-leukocyte antibody marker showed abundant leukocyte infiltrations in SVCV-infected rag1(-/-) fish, coinciding with increased transcript expression of genes related to NK-cells and macrophages, suggesting that these genes played a key role in the enhanced immune response of rag1(-/-) zebra fish to SVCV lethal infection. Overall, we present evidence that indicates that rag1(-/-) zebra fish acquire an antiviral alert state while they reach adulthood in the absence of adaptive immunity. This antiviral state was characterized by (i) a more rapid response to viral infection, which resulted in increased survival, (ii) the involvement of NK-cell- and macrophage-mediated transcript responses rather than B- and/or T-cell dependent cells, and (iii) enhanced apoptosis, described here for the first time, as well as the similar modulation of multigene family/interferon-related genes previously associated to fish that survived lethal viral infections. From this and other studies, it might be concluded that some of the characteristics of mammalian trained immunity are present in lower vertebrates.
dc.language.iso eng
dc.publisher FRONTIERS MEDIA SA
dc.rights Atribución/Reconocimiento 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by/4.0/deed.es *
dc.title Zebra Fish Lacking Adaptive Immunity Acquire an Antiviral Alert State Characterized by Upregulated Gene Expression of Apoptosis, Multigene Families, and Interferon-Related Genes
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 28243233
dc.relation.publisherversion http://journal.frontiersin.org/article/10.3389/fimmu.2017.00121/full
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.3389/fimmu.2017.00121
dc.journal.title Frontiers in Immunology


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