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Whole transcriptome approach to evaluate the effect of aluminium hydroxide in ovine encephalon

Aluminium 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 commercia...

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Autores principales: Varela-Martínez, Endika, Bilbao-Arribas, Martin, Abendaño, Naiara, Asín, Javier, Pérez, Marta, de Andrés, Damián, Luján, Lluís, Jugo, Begoña M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7498608/
https://www.ncbi.nlm.nih.gov/pubmed/32943671
http://dx.doi.org/10.1038/s41598-020-71905-y
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author Varela-Martínez, Endika
Bilbao-Arribas, Martin
Abendaño, Naiara
Asín, Javier
Pérez, Marta
de Andrés, Damián
Luján, Lluís
Jugo, Begoña M.
author_facet Varela-Martínez, Endika
Bilbao-Arribas, Martin
Abendaño, Naiara
Asín, Javier
Pérez, Marta
de Andrés, Damián
Luján, Lluís
Jugo, Begoña M.
author_sort Varela-Martínez, Endika
collection PubMed
description Aluminium 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.
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spelling pubmed-74986082020-09-18 Whole transcriptome approach to evaluate the effect of aluminium hydroxide in ovine encephalon Varela-Martínez, Endika Bilbao-Arribas, Martin Abendaño, Naiara Asín, Javier Pérez, Marta de Andrés, Damián Luján, Lluís Jugo, Begoña M. Sci Rep Article Aluminium 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. Nature Publishing Group UK 2020-09-17 /pmc/articles/PMC7498608/ /pubmed/32943671 http://dx.doi.org/10.1038/s41598-020-71905-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Varela-Martínez, Endika
Bilbao-Arribas, Martin
Abendaño, Naiara
Asín, Javier
Pérez, Marta
de Andrés, Damián
Luján, Lluís
Jugo, Begoña M.
Whole transcriptome approach to evaluate the effect of aluminium hydroxide in ovine encephalon
title Whole transcriptome approach to evaluate the effect of aluminium hydroxide in ovine encephalon
title_full Whole transcriptome approach to evaluate the effect of aluminium hydroxide in ovine encephalon
title_fullStr Whole transcriptome approach to evaluate the effect of aluminium hydroxide in ovine encephalon
title_full_unstemmed Whole transcriptome approach to evaluate the effect of aluminium hydroxide in ovine encephalon
title_short Whole transcriptome approach to evaluate the effect of aluminium hydroxide in ovine encephalon
title_sort whole transcriptome approach to evaluate the effect of aluminium hydroxide in ovine encephalon
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7498608/
https://www.ncbi.nlm.nih.gov/pubmed/32943671
http://dx.doi.org/10.1038/s41598-020-71905-y
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