Lopez Bryan Irvine, Santiago Kier Gumangan, Lee Donghui, Ha Seungmin, Seo Kangseok
Division of Animal Genomics and Bioinformatics, National Institute of Animal Science, Rural Development Administration, Wanju 55365, Korea.
Department of Animal Science and Technology, Sunchon National University, Suncheon 57922, Korea.
Animals (Basel). 2020 Feb 21;10(2):344. doi: 10.3390/ani10020344.
Immune response of 107 vaccinated Holstein cattle was initially obtained prior to the ELISA test. Five cattle with high and low bovine viral diarrhea virus (BVDV) type I antibody were identified as the final experimental animals. Blood samples from these animals were then utilized to determine significant differentially expressed genes (DEGs) using the RNA-seq transcriptome analysis and enrichment analysis. Our analysis identified 261 DEGs in cattle identified as experimental animals. Functional enrichment analysis in gene ontology (GO) annotations and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways revealed the DEGs potentially induced by the inactivated BVDV type I vaccine, and might be responsible for the host immune responses. Our findings suggested that inactivated vaccine induced upregulation of genes involved in different GO annotations, including antigen processing and presentation of peptide antigen (via MHC class I), immune response, and positive regulation of interferon-gamma production. The observed downregulation of other genes involved in immune response might be due to inhibition of toll-like receptors (TLRs) by the upregulation of the Bcl-3 gene. Meanwhile, the result of KEGG pathways revealed that the majority of DEGs were upregulated and enriched to different pathways, including cytokine-cytokine receptor interaction, platelet activation, extracellular matrix (ECM) receptor interaction, hematopoietic cell lineage, and ATP-binding cassette (ABC) transporters. These significant pathways supported our initial findings and are known to play a vital role in shaping adaptive immunity against BVDV type 1. In addition, type 1 diabetes mellitus pathways tended to be significantly enriched. Thus, further studies are needed to investigate the prevalence of type 1 diabetes mellitus in cattle vaccinated with inactivated and live BVDV vaccine.
107头接种疫苗的荷斯坦奶牛的免疫反应最初是在ELISA检测之前获得的。确定了5头I型牛病毒性腹泻病毒(BVDV)抗体水平高和低的奶牛作为最终实验动物。然后利用这些动物的血样,通过RNA测序转录组分析和富集分析来确定显著差异表达基因(DEG)。我们的分析在被确定为实验动物的奶牛中鉴定出261个DEG。基因本体论(GO)注释和京都基因与基因组百科全书(KEGG)通路中的功能富集分析揭示了可能由I型灭活BVDV疫苗诱导的DEG,它们可能负责宿主的免疫反应。我们的研究结果表明,灭活疫苗诱导了参与不同GO注释的基因上调,包括肽抗原的抗原加工和呈递(通过I类MHC)、免疫反应以及干扰素-γ产生的正调控。观察到的其他参与免疫反应的基因下调可能是由于Bcl-3基因上调对Toll样受体(TLR)的抑制。同时,KEGG通路的结果显示,大多数DEG上调并富集到不同的通路,包括细胞因子-细胞因子受体相互作用、血小板活化、细胞外基质(ECM)受体相互作用、造血细胞谱系和ATP结合盒(ABC)转运蛋白。这些重要通路支持了我们的初步发现,并且已知在形成针对I型BVDV的适应性免疫中发挥重要作用。此外,1型糖尿病通路倾向于显著富集。因此,需要进一步研究来调查接种灭活和活BVDV疫苗的奶牛中1型糖尿病的患病率。