Zhao Qingyao, Wang Jiahao, Ma Fuping, Chen Quanzhen, Liu Huatao, Yang Jinyan, Chen Siqian, Tang Yongjie, Mi Siyuan, Wang Lulu, Wang Xini, Liu Guohong, Xing Kai, Yu Ying, Wang Chuduan
State Key Laboratory of Animal Biotech Breeding, National Engineering Laboratory for Animal Breeding, and Key Laboratory of Animal Genetics, Breeding and Reproduction, Ministry of Agriculture & College of Animal Science and Technology, China Agricultural University, Beijing, 100193, P. R. China.
J Anim Sci Biotechnol. 2025 May 19;16(1):69. doi: 10.1186/s40104-025-01184-y.
Viral diseases have profoundly influenced the sustainable development of the swine farming industry. With the development of genomics technology, the combination of transcriptome, genetic variation, immune response, and QTL mapping data to illustrate the interactions between pathogen and host immune system, will be an effective tool for identification of disease resistance genes in pigs. The immune system of an organism is the source of disease resistance in livestock, consisting of various immune tissues, as well as the immune cells and cytokines they produced. However, comprehensive systematic studies on transcriptome of porcine immune tissues are still rare. Poly(I:C), as a viral mimic, is commonly used to study immune responses of the body during viral infections, and serves as a valuable tool for investigating immune mechanisms in swine.
WGCNA analysis identified core immune genes across six immune tissues (bone marrow, jejunum, lymph node, PBMC, spleen, thymus) in Landrace pigs, which are also crucial for the development of PBMCs. The examination of the changes in the proportion of immune cells during three developmental stages (1-month-old, 4-month-old, 7-month-old) shows a shift from innate immunity to humoral immunity. By integrating different epigenetic genomics datasets, we identified several core immune genes and their causal variants, including IFI44, IFIT5, EIF2AK2 and others, which are closely related to immune development and response. Functional validation studies reveal that the IFI44 gene acts as a negative regulator of the antiviral response; its inhibition effect significantly reduced Poly(I:C)-induced cell necrosis, while enhancing apoptosis to combat viral infections.
Our study elucidated the fundamental transcriptional program in porcine immune tissues and the immunodynamics underlying development of PBMCs, identifying many core immune genes, including IFI44, which plays a critical negative regulator role in the antiviral response, providing valuable insights for breeding programs aimed at enhancing pig disease resistance.
病毒性疾病对养猪业的可持续发展产生了深远影响。随着基因组学技术的发展,结合转录组、遗传变异、免疫反应和QTL定位数据来阐明病原体与宿主免疫系统之间的相互作用,将成为鉴定猪抗病基因的有效工具。生物体的免疫系统是家畜抗病性的来源,由各种免疫组织以及它们产生的免疫细胞和细胞因子组成。然而,对猪免疫组织转录组的全面系统研究仍然很少。聚肌胞苷酸(Poly(I:C))作为一种病毒模拟物,常用于研究病毒感染期间机体的免疫反应,是研究猪免疫机制的宝贵工具。
WGCNA分析确定了长白猪六个免疫组织(骨髓、空肠、淋巴结、外周血单核细胞、脾脏、胸腺)中的核心免疫基因,这些基因对PBMC的发育也至关重要。对三个发育阶段(1月龄、4月龄、7月龄)免疫细胞比例变化的检测表明,免疫反应从先天免疫向体液免疫转变。通过整合不同的表观遗传基因组数据集,我们鉴定了几个核心免疫基因及其因果变异,包括IFI44、IFIT5、EIF2AK2等,它们与免疫发育和反应密切相关。功能验证研究表明,IFI44基因作为抗病毒反应的负调节因子;其抑制作用显著降低了Poly(I:C)诱导的细胞坏死,同时增强了细胞凋亡以对抗病毒感染。
我们的研究阐明了猪免疫组织中的基本转录程序以及PBMC发育的免疫动力学,鉴定了许多核心免疫基因,包括在抗病毒反应中起关键负调节作用的IFI44,为旨在提高猪抗病性的育种计划提供了有价值的见解。