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Transcriptomic analysis of the stress response to weaning at housing in bovine leukocytes using RNA-seq technology

BACKGROUND: Weaning of beef calves is a necessary husbandry practice and involves separating the calf from its mother, resulting in numerous stressful events including dietary change, social reorganisation and the cessation of the maternal-offspring bond and is often accompanied by housing. While mu...

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Autores principales: O’Loughlin, Aran, Lynn, David J, McGee, Mark, Doyle, Sean, McCabe, Matthew, Earley, Bernadette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583219/
https://www.ncbi.nlm.nih.gov/pubmed/22708644
http://dx.doi.org/10.1186/1471-2164-13-250
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author O’Loughlin, Aran
Lynn, David J
McGee, Mark
Doyle, Sean
McCabe, Matthew
Earley, Bernadette
author_facet O’Loughlin, Aran
Lynn, David J
McGee, Mark
Doyle, Sean
McCabe, Matthew
Earley, Bernadette
author_sort O’Loughlin, Aran
collection PubMed
description BACKGROUND: Weaning of beef calves is a necessary husbandry practice and involves separating the calf from its mother, resulting in numerous stressful events including dietary change, social reorganisation and the cessation of the maternal-offspring bond and is often accompanied by housing. While much recent research has focused on the physiological response of the bovine immune system to stress in recent years, little is known about the molecular mechanisms modulating the immune response. Therefore, the objective of this study was to provide new insights into the molecular mechanisms underlying the physiological response to weaning at housing in beef calves using Illumina RNA-seq. RESULTS: The leukocyte transcriptome was significantly altered for at least 7 days following either housing or weaning at housing. Analysis of differentially expressed genes revealed that four main pathways, cytokine signalling, transmembrane transport, haemostasis and G-protein-coupled receptor (GPRC) signalling were differentially regulated between control and weaned calves and underwent significant transcriptomic alterations in response to weaning stress on day 1, 2 and 7. Of particular note, chemokines, cytokines and integrins were consistently found to be up-regulated on each day following weaning. Evidence for alternative splicing of genes was also detected, indicating a number of genes involved in the innate and adaptive immune response may be alternatively transcribed, including those responsible for toll receptor cascades and T cell receptor signalling. CONCLUSIONS: This study represents the first application of RNA-Seq technology for genomic studies in bovine leukocytes in response to weaning stress. Weaning stress induces the activation of a number of cytokine, chemokine and integrin transcripts and may alter the immune system whereby the ability of a number of cells of the innate and adaptive immune system to locate and destroy pathogens is transcriptionally enhanced. Stress alters the homeostasis of the transcriptomic environment of leukocytes for at least 7 days following weaning, indicating long term effects of stress exposure in the bovine. The identification of gene signature networks that are stress activated provides a mechanistic framework to characterise the multifaceted nature of weaning stress adaptation in beef calves. Thus, capturing subtle transcriptomic changes provides insight into the molecular mechanisms that underlie the physiological response to weaning stress.
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spelling pubmed-35832192013-02-28 Transcriptomic analysis of the stress response to weaning at housing in bovine leukocytes using RNA-seq technology O’Loughlin, Aran Lynn, David J McGee, Mark Doyle, Sean McCabe, Matthew Earley, Bernadette BMC Genomics Research Article BACKGROUND: Weaning of beef calves is a necessary husbandry practice and involves separating the calf from its mother, resulting in numerous stressful events including dietary change, social reorganisation and the cessation of the maternal-offspring bond and is often accompanied by housing. While much recent research has focused on the physiological response of the bovine immune system to stress in recent years, little is known about the molecular mechanisms modulating the immune response. Therefore, the objective of this study was to provide new insights into the molecular mechanisms underlying the physiological response to weaning at housing in beef calves using Illumina RNA-seq. RESULTS: The leukocyte transcriptome was significantly altered for at least 7 days following either housing or weaning at housing. Analysis of differentially expressed genes revealed that four main pathways, cytokine signalling, transmembrane transport, haemostasis and G-protein-coupled receptor (GPRC) signalling were differentially regulated between control and weaned calves and underwent significant transcriptomic alterations in response to weaning stress on day 1, 2 and 7. Of particular note, chemokines, cytokines and integrins were consistently found to be up-regulated on each day following weaning. Evidence for alternative splicing of genes was also detected, indicating a number of genes involved in the innate and adaptive immune response may be alternatively transcribed, including those responsible for toll receptor cascades and T cell receptor signalling. CONCLUSIONS: This study represents the first application of RNA-Seq technology for genomic studies in bovine leukocytes in response to weaning stress. Weaning stress induces the activation of a number of cytokine, chemokine and integrin transcripts and may alter the immune system whereby the ability of a number of cells of the innate and adaptive immune system to locate and destroy pathogens is transcriptionally enhanced. Stress alters the homeostasis of the transcriptomic environment of leukocytes for at least 7 days following weaning, indicating long term effects of stress exposure in the bovine. The identification of gene signature networks that are stress activated provides a mechanistic framework to characterise the multifaceted nature of weaning stress adaptation in beef calves. Thus, capturing subtle transcriptomic changes provides insight into the molecular mechanisms that underlie the physiological response to weaning stress. BioMed Central 2012-06-18 /pmc/articles/PMC3583219/ /pubmed/22708644 http://dx.doi.org/10.1186/1471-2164-13-250 Text en Copyright © 2012 O'Loughlin 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
O’Loughlin, Aran
Lynn, David J
McGee, Mark
Doyle, Sean
McCabe, Matthew
Earley, Bernadette
Transcriptomic analysis of the stress response to weaning at housing in bovine leukocytes using RNA-seq technology
title Transcriptomic analysis of the stress response to weaning at housing in bovine leukocytes using RNA-seq technology
title_full Transcriptomic analysis of the stress response to weaning at housing in bovine leukocytes using RNA-seq technology
title_fullStr Transcriptomic analysis of the stress response to weaning at housing in bovine leukocytes using RNA-seq technology
title_full_unstemmed Transcriptomic analysis of the stress response to weaning at housing in bovine leukocytes using RNA-seq technology
title_short Transcriptomic analysis of the stress response to weaning at housing in bovine leukocytes using RNA-seq technology
title_sort transcriptomic analysis of the stress response to weaning at housing in bovine leukocytes using rna-seq technology
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583219/
https://www.ncbi.nlm.nih.gov/pubmed/22708644
http://dx.doi.org/10.1186/1471-2164-13-250
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