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The peripheral blood transcriptome reflects variations in immunity traits in swine: towards the identification of biomarkers

BACKGROUND: Immune traits (ITs) are potentially relevant criteria to characterize an individual’s immune response. Our aim was to investigate whether the peripheral blood transcriptome can provide a significant and comprehensive view of IT variations in pig. RESULTS: Sixty-day-old Large White pigs c...

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Autores principales: Mach, Núria, Gao, Yu, Lemonnier, Gaëtan, Lecardonnel, Jérôme, Oswald, Isabelle P, Estellé, Jordi, Rogel-Gaillard, Claire
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878494/
https://www.ncbi.nlm.nih.gov/pubmed/24341289
http://dx.doi.org/10.1186/1471-2164-14-894
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author Mach, Núria
Gao, Yu
Lemonnier, Gaëtan
Lecardonnel, Jérôme
Oswald, Isabelle P
Estellé, Jordi
Rogel-Gaillard, Claire
author_facet Mach, Núria
Gao, Yu
Lemonnier, Gaëtan
Lecardonnel, Jérôme
Oswald, Isabelle P
Estellé, Jordi
Rogel-Gaillard, Claire
author_sort Mach, Núria
collection PubMed
description BACKGROUND: Immune traits (ITs) are potentially relevant criteria to characterize an individual’s immune response. Our aim was to investigate whether the peripheral blood transcriptome can provide a significant and comprehensive view of IT variations in pig. RESULTS: Sixty-day-old Large White pigs classified as extreme for in vitro production of IL2, IL10, IFNγ and TNFα, phagocytosis activity, in vivo CD4(-)/CD8(+) or TCRγδ + cell counts, and anti-Mycoplasma antibody levels were chosen to perform a blood transcriptome analysis with a porcine generic array enriched with immunity-related genes. Differentially expressed (DE) genes for in vitro production of IL2 and IL10, phagocytosis activity and CD4(-)/CD8(+) cell counts were identified. Gene set enrichment analysis revealed a significant over-representation of immune response functions. To validate the microarray-based results, a subset of DE genes was confirmed by RT-qPCR. An independent set of 74 animals was used to validate the covariation between gene expression levels and ITs. Five potential gene biomarkers were found for prediction of IL2 (RALGDS), phagocytosis (ALOX12) or CD4(-)/CD8(+) cell count (GNLY, KLRG1 and CX3CR1). On average, these biomarkers performed with a sensitivity of 79% and a specificity of 86%. CONCLUSIONS: Our results confirmed that gene expression profiling in blood represents a relevant molecular phenotype to refine ITs in pig and to identify potential biomarkers that can provide new insights into immune response analysis.
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spelling pubmed-38784942014-01-03 The peripheral blood transcriptome reflects variations in immunity traits in swine: towards the identification of biomarkers Mach, Núria Gao, Yu Lemonnier, Gaëtan Lecardonnel, Jérôme Oswald, Isabelle P Estellé, Jordi Rogel-Gaillard, Claire BMC Genomics Research Article BACKGROUND: Immune traits (ITs) are potentially relevant criteria to characterize an individual’s immune response. Our aim was to investigate whether the peripheral blood transcriptome can provide a significant and comprehensive view of IT variations in pig. RESULTS: Sixty-day-old Large White pigs classified as extreme for in vitro production of IL2, IL10, IFNγ and TNFα, phagocytosis activity, in vivo CD4(-)/CD8(+) or TCRγδ + cell counts, and anti-Mycoplasma antibody levels were chosen to perform a blood transcriptome analysis with a porcine generic array enriched with immunity-related genes. Differentially expressed (DE) genes for in vitro production of IL2 and IL10, phagocytosis activity and CD4(-)/CD8(+) cell counts were identified. Gene set enrichment analysis revealed a significant over-representation of immune response functions. To validate the microarray-based results, a subset of DE genes was confirmed by RT-qPCR. An independent set of 74 animals was used to validate the covariation between gene expression levels and ITs. Five potential gene biomarkers were found for prediction of IL2 (RALGDS), phagocytosis (ALOX12) or CD4(-)/CD8(+) cell count (GNLY, KLRG1 and CX3CR1). On average, these biomarkers performed with a sensitivity of 79% and a specificity of 86%. CONCLUSIONS: Our results confirmed that gene expression profiling in blood represents a relevant molecular phenotype to refine ITs in pig and to identify potential biomarkers that can provide new insights into immune response analysis. BioMed Central 2013-12-17 /pmc/articles/PMC3878494/ /pubmed/24341289 http://dx.doi.org/10.1186/1471-2164-14-894 Text en Copyright © 2013 Mach et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mach, Núria
Gao, Yu
Lemonnier, Gaëtan
Lecardonnel, Jérôme
Oswald, Isabelle P
Estellé, Jordi
Rogel-Gaillard, Claire
The peripheral blood transcriptome reflects variations in immunity traits in swine: towards the identification of biomarkers
title The peripheral blood transcriptome reflects variations in immunity traits in swine: towards the identification of biomarkers
title_full The peripheral blood transcriptome reflects variations in immunity traits in swine: towards the identification of biomarkers
title_fullStr The peripheral blood transcriptome reflects variations in immunity traits in swine: towards the identification of biomarkers
title_full_unstemmed The peripheral blood transcriptome reflects variations in immunity traits in swine: towards the identification of biomarkers
title_short The peripheral blood transcriptome reflects variations in immunity traits in swine: towards the identification of biomarkers
title_sort peripheral blood transcriptome reflects variations in immunity traits in swine: towards the identification of biomarkers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878494/
https://www.ncbi.nlm.nih.gov/pubmed/24341289
http://dx.doi.org/10.1186/1471-2164-14-894
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