Animal and Bioscience Research Department, Animal & Grassland Research and Innovation Centre, Grange, Dunsany, Co. Meath, Ireland.
BMC Genomics. 2012 Jun 18;13:250. doi: 10.1186/1471-2164-13-250.
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.
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.
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.
牛犊断奶是一种必要的饲养实践,涉及将小牛从其母亲身边分离,导致许多应激事件,包括饮食改变、社会重组以及母子关系的终止,通常还伴随着住房变化。尽管近年来许多研究都集中在牛的免疫系统对压力的生理反应上,但对于调节免疫反应的分子机制却知之甚少。因此,本研究的目的是利用 Illumina RNA-seq 技术,为牛犊在住房中断奶的生理反应的分子机制提供新的见解。
无论是住房还是住房断奶后,白细胞转录组至少在 7 天内发生了显著改变。差异表达基因分析表明,在断奶应激后第 1、2 和 7 天,有 4 个主要途径(细胞因子信号、跨膜转运、止血和 G 蛋白偶联受体(GPRC)信号)在对照组和断奶组之间存在差异调节,并发生了显著的转录组改变。值得注意的是,趋化因子、细胞因子和整合素在断奶后每天都被发现上调。还检测到基因的选择性剪接证据,表明一些参与先天和适应性免疫反应的基因可能被选择性转录,包括那些负责 Toll 受体级联和 T 细胞受体信号的基因。
本研究代表了 RNA-Seq 技术在牛白细胞对断奶应激反应的基因组研究中的首次应用。断奶应激诱导了大量细胞因子、趋化因子和整合素转录本的激活,并可能改变免疫系统,使先天和适应性免疫系统的许多细胞能够定位和破坏病原体的能力在转录水平上增强。应激至少在断奶后 7 天内改变了白细胞转录组的动态平衡,表明应激暴露对牛的长期影响。鉴定应激激活的基因签名网络为特征性地描述牛犊断奶应激适应的多方面性质提供了机制框架。因此,捕捉细微的转录组变化为理解断奶应激反应的分子机制提供了深入的见解。