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dc.contributor.authorVarela Martínez, Endika ORCID
dc.contributor.authorBilbao Arribas, Martín
dc.contributor.authorAbendaño Carbajo, Naiara ORCID
dc.contributor.authorAsín, Javier
dc.contributor.authorPérez, Marta Maria
dc.contributor.authorDe Andrés, Damián
dc.contributor.authorLuján, Lluís
dc.contributor.authorJugo Orrantia, Begoña Marina ORCID
dc.date.accessioned2021-02-24T09:00:21Z
dc.date.available2021-02-24T09:00:21Z
dc.date.issued2020-09-17
dc.identifier.citationScientific Reports 10(1) : (2020) // Article ID 15240es_ES
dc.identifier.issn2045-2322
dc.identifier.urihttp://hdl.handle.net/10810/50310
dc.description.abstractAluminium hydroxide adjuvants are crucial for livestock and human vaccines. Few studies have analysed their effect on the central nervous system in vivo. In this work, lambs received three different treatments of parallel subcutaneous inoculations during 16 months with aluminium-containing commercial vaccines, an equivalent dose of aluminium hydroxide or mock injections. Brain samples were sequenced by RNA-seq and miRNA-seq for the expression analysis of mRNAs, long non-coding RNAs and microRNAs and three expression comparisons were made. Although few differentially expressed genes were identified, some dysregulated genes by aluminium hydroxide alone were linked to neurological functions, the lncRNA TUNA among them, or were enriched in mitochondrial energy metabolism related functions. In the same way, the miRNA expression was mainly disrupted by the adjuvant alone treatment. Some differentially expressed miRNAs had been previously linked to neurological diseases, oxidative stress and apoptosis. In brief, in this study aluminium hydroxide alone altered the transcriptome of the encephalon to a higher degree than commercial vaccines that present a milder effect. The expression changes in the animals inoculated with aluminium hydroxide suggest mitochondrial disfunction. Further research is needed to elucidate to which extent these changes could have pathological consequences.es_ES
dc.description.sponsorshipThis work was supported by the Spanish Ministry of Economy grant [MINECO project AGL2013-49137-C3 to BMJ, LL and DA]; University of the Basque Country (UPV/EHU) predoctoral fellowships [PIF15/361 to EV-M and PIF17/306 to MB-A]; and University of the Basque Country (UPV/EHU) postdoctoral fellowship [ESPDOC16/43 to NA]. Thanks to M. Ortega for technical help.es_ES
dc.language.isoenges_ES
dc.publisherNaturees_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/AGL2013-49137-C3es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectlong noncoding RNAses_ES
dc.subjectcentral-nervous-systemes_ES
dc.subjectoxidative stresses_ES
dc.subjectneuronal developmentes_ES
dc.subjectprotein familieses_ES
dc.subjectsequencees_ES
dc.subjectgeneses_ES
dc.subjectmodeles_ES
dc.subjectneurotoxicityes_ES
dc.subjectphysiologyes_ES
dc.titleWhole Transcriptome Approach to Evaluate the Effect of Aluminium Hydroxide in Ovine Encephalones_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderThis article is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0)es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://www.nature.com/articles/s41598-020-71905-yes_ES
dc.identifier.doi10.1038/s41598-020-71905-y
dc.departamentoesGenética, antropología física y fisiología animales_ES
dc.departamentoeuGenetika,antropologia fisikoa eta animalien fisiologiaes_ES


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