NK-lysin peptides ameliorate viral encephalopathy and retinopathy disease signs and provide partial protection against nodavirus infection in European sea bass

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Microbioloxía e Parasitoloxíagl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Instituto de Acuiculturagl
dc.contributor.authorValero Cuesta, Yulema
dc.contributor.authorGonzález Fernández, Carmen
dc.contributor.authorCárdenas, Constanza
dc.contributor.authorGuzmán, Fanny
dc.contributor.authorLeón, Rosa
dc.contributor.authorCuesta, Alberto
dc.date.accessioned2021-06-24T08:21:09Z
dc.date.available2021-06-24T08:21:09Z
dc.date.issued2021
dc.description.abstractAntimicrobial peptides (AMP) comprise a wide range of small molecules with direct antibacterial activity and immunostimulatory role and are proposed as promising substitutes of the antibiotics. Additionally, they also exert a role against other pathogens such as viruses and fungi less evaluated. NK-lysin, a human granulysin orthologue, possess a double function, taking part in the innate immunity as AMP and also as direct effector in the cell-mediated cytotoxic (CMC) response. This molecule is suggested as a pivotal molecule involved in the defence upon nervous necrosis virus (NNV), an epizootic virus provoking serious problems in welfare and health status in Asian and Mediterranean fish destined to human consumption. Having proved that NK-lysin derived peptides (NKLPs) have a direct antiviral activity against NNV in vitro, we aimed to evaluate their potential use as a prophylactic treatment for European sea bass (Dicentrarchus labrax), one of the most susceptible cultured-fish species. Thus, intramuscular injection of synthetic NKLPs resulted in a very low transcriptional response of some innate and adaptive immune markers. However, the injection of NKLPs ameliorated disease signs and increased fish survival upon challenge with pathogenic NNV. Although NKLPs showed promising results in treatments against NNV, more efforts are needed to understand their mechanisms of action and their applicability to the aquaculture industrygl
dc.description.peerreviewedSIgl
dc.description.sponsorshipThis work was supported by Ministerio de Economía y Competitividad (MINECO; grant AGL2016-74866-C3-1-R with FEDER co-funds), Agencia Española de Investigación (PID2019-105522 GB-I00), Fundación Séneca, Grupo de Excelencia de la Región de Murcia (grant 19883/GERM/15) and National Commission for Scientific & Technological Research Chile (grant FONDECYT N° 1170379)gl
dc.identifier.citationAntiviral Research, 192 (2021), 105104. https://doi.org/10.1016/j.antiviral.2021.105104gl
dc.identifier.doi10.1016/j.antiviral.2021.105104
dc.identifier.issn0166-3542
dc.identifier.urihttp://hdl.handle.net/10347/26512
dc.language.isoenggl
dc.publisherElseviergl
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/AGL2016-74866-C3-1-R/ESgl
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-105522GB-I00/ES/HERRAMIENTAS, MECANISMOS, MEDIADORES Y DISRUPTORES DE LA RESPUESTA INMUNITARIA DE PECES FRENTE A NODAVIRUSgl
dc.relation.publisherversionhttps://doi.org/10.1016/j.antiviral.2021.105104gl
dc.rights© 2021 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)gl
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectAntimicrobial peptides (AMP)gl
dc.subjectNK-lysingl
dc.subjectNervous necrosis virusgl
dc.subjectEuropean sea bassgl
dc.subjectTeleost fishgl
dc.titleNK-lysin peptides ameliorate viral encephalopathy and retinopathy disease signs and provide partial protection against nodavirus infection in European sea bassgl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
relation.isAuthorOfPublication597b57e6-596f-4ae2-92a8-96b4028fdace
relation.isAuthorOfPublication.latestForDiscovery597b57e6-596f-4ae2-92a8-96b4028fdace

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