Cargando…

Genetic architecture of innate and adaptive immune cells in pigs

Pig industry is facing new challenges that make necessary to reorient breeding programs to produce more robust and resilient pig populations. The aim of the present work was to study the genetic determinism of lymphocyte subpopulations in the peripheral blood of pigs and identify genomic regions and...

Descripción completa

Detalles Bibliográficos
Autores principales: Ballester, Maria, Jové-Juncà, Teodor, Pascual, Afra, López-Serrano, Sergi, Crespo-Piazuelo, Daniel, Hernández-Banqué, Carles, González-Rodríguez, Olga, Ramayo-Caldas, Yuliaxis, Quintanilla, Raquel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939681/
https://www.ncbi.nlm.nih.gov/pubmed/36814923
http://dx.doi.org/10.3389/fimmu.2023.1058346
_version_ 1784890910853562368
author Ballester, Maria
Jové-Juncà, Teodor
Pascual, Afra
López-Serrano, Sergi
Crespo-Piazuelo, Daniel
Hernández-Banqué, Carles
González-Rodríguez, Olga
Ramayo-Caldas, Yuliaxis
Quintanilla, Raquel
author_facet Ballester, Maria
Jové-Juncà, Teodor
Pascual, Afra
López-Serrano, Sergi
Crespo-Piazuelo, Daniel
Hernández-Banqué, Carles
González-Rodríguez, Olga
Ramayo-Caldas, Yuliaxis
Quintanilla, Raquel
author_sort Ballester, Maria
collection PubMed
description Pig industry is facing new challenges that make necessary to reorient breeding programs to produce more robust and resilient pig populations. The aim of the present work was to study the genetic determinism of lymphocyte subpopulations in the peripheral blood of pigs and identify genomic regions and biomarkers associated to them. For this purpose, we stained peripheral blood mononuclear cells to measure ten immune-cell-related traits including the relative abundance of different populations of lymphocytes, the proportions of CD4(+) T cells and CD8(+) T cells, and the ratio of CD4(+)/CD8(+) T cells from 391 healthy Duroc piglets aged 8 weeks. Medium to high heritabilities were observed for the ten immune-cell-related traits and significant genetic correlations were obtained between the proportion of some lymphocytes populations. A genome-wide association study pointed out 32 SNPs located at four chromosomal regions on pig chromosomes SSC3, SSC5, SSC8, and SSCX as significantly associated to T-helper cells, memory T-helper cells and γδ T cells. Several genes previously identified in human association studies for the same or related traits were located in the associated regions, and were proposed as candidate genes to explain the variation of T cell populations such as CD4, CD8A, CD8B, KLRC2, RMND5A and VPS24. The transcriptome analysis of whole blood samples from animals with extreme proportions of γδ T, T-helper and memory T-helper cells identified differentially expressed genes (CAPG, TCF7L1, KLRD1 and CD4) located into the associated regions. In addition, differentially expressed genes specific of different T cells subpopulations were identified such as SOX13 and WC1 genes for γδ T cells. Our results enhance the knowledge about the genetic control of lymphocyte traits that could be considered to optimize the induction of immune responses to vaccines against pathogens. Furthermore, they open the possibility of applying effective selection programs for improving immunocompetence in pigs and support the use of the pig as a very reliable human biomedical model.
format Online
Article
Text
id pubmed-9939681
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-99396812023-02-21 Genetic architecture of innate and adaptive immune cells in pigs Ballester, Maria Jové-Juncà, Teodor Pascual, Afra López-Serrano, Sergi Crespo-Piazuelo, Daniel Hernández-Banqué, Carles González-Rodríguez, Olga Ramayo-Caldas, Yuliaxis Quintanilla, Raquel Front Immunol Immunology Pig industry is facing new challenges that make necessary to reorient breeding programs to produce more robust and resilient pig populations. The aim of the present work was to study the genetic determinism of lymphocyte subpopulations in the peripheral blood of pigs and identify genomic regions and biomarkers associated to them. For this purpose, we stained peripheral blood mononuclear cells to measure ten immune-cell-related traits including the relative abundance of different populations of lymphocytes, the proportions of CD4(+) T cells and CD8(+) T cells, and the ratio of CD4(+)/CD8(+) T cells from 391 healthy Duroc piglets aged 8 weeks. Medium to high heritabilities were observed for the ten immune-cell-related traits and significant genetic correlations were obtained between the proportion of some lymphocytes populations. A genome-wide association study pointed out 32 SNPs located at four chromosomal regions on pig chromosomes SSC3, SSC5, SSC8, and SSCX as significantly associated to T-helper cells, memory T-helper cells and γδ T cells. Several genes previously identified in human association studies for the same or related traits were located in the associated regions, and were proposed as candidate genes to explain the variation of T cell populations such as CD4, CD8A, CD8B, KLRC2, RMND5A and VPS24. The transcriptome analysis of whole blood samples from animals with extreme proportions of γδ T, T-helper and memory T-helper cells identified differentially expressed genes (CAPG, TCF7L1, KLRD1 and CD4) located into the associated regions. In addition, differentially expressed genes specific of different T cells subpopulations were identified such as SOX13 and WC1 genes for γδ T cells. Our results enhance the knowledge about the genetic control of lymphocyte traits that could be considered to optimize the induction of immune responses to vaccines against pathogens. Furthermore, they open the possibility of applying effective selection programs for improving immunocompetence in pigs and support the use of the pig as a very reliable human biomedical model. Frontiers Media S.A. 2023-02-06 /pmc/articles/PMC9939681/ /pubmed/36814923 http://dx.doi.org/10.3389/fimmu.2023.1058346 Text en Copyright © 2023 Ballester, Jové-Juncà, Pascual, López-Serrano, Crespo-Piazuelo, Hernández-Banqué, González-Rodríguez, Ramayo-Caldas and Quintanilla https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Ballester, Maria
Jové-Juncà, Teodor
Pascual, Afra
López-Serrano, Sergi
Crespo-Piazuelo, Daniel
Hernández-Banqué, Carles
González-Rodríguez, Olga
Ramayo-Caldas, Yuliaxis
Quintanilla, Raquel
Genetic architecture of innate and adaptive immune cells in pigs
title Genetic architecture of innate and adaptive immune cells in pigs
title_full Genetic architecture of innate and adaptive immune cells in pigs
title_fullStr Genetic architecture of innate and adaptive immune cells in pigs
title_full_unstemmed Genetic architecture of innate and adaptive immune cells in pigs
title_short Genetic architecture of innate and adaptive immune cells in pigs
title_sort genetic architecture of innate and adaptive immune cells in pigs
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939681/
https://www.ncbi.nlm.nih.gov/pubmed/36814923
http://dx.doi.org/10.3389/fimmu.2023.1058346
work_keys_str_mv AT ballestermaria geneticarchitectureofinnateandadaptiveimmunecellsinpigs
AT jovejuncateodor geneticarchitectureofinnateandadaptiveimmunecellsinpigs
AT pascualafra geneticarchitectureofinnateandadaptiveimmunecellsinpigs
AT lopezserranosergi geneticarchitectureofinnateandadaptiveimmunecellsinpigs
AT crespopiazuelodaniel geneticarchitectureofinnateandadaptiveimmunecellsinpigs
AT hernandezbanquecarles geneticarchitectureofinnateandadaptiveimmunecellsinpigs
AT gonzalezrodriguezolga geneticarchitectureofinnateandadaptiveimmunecellsinpigs
AT ramayocaldasyuliaxis geneticarchitectureofinnateandadaptiveimmunecellsinpigs
AT quintanillaraquel geneticarchitectureofinnateandadaptiveimmunecellsinpigs