Department of Pathobiology, Ontario Veterinary College, University of Guelph, Guelph, ON, N1G 2W1, Canada.
Department of Human Genetics, McGill University, Montreal, QC, H3A 0E7, Canada.
Sci Rep. 2021 Oct 14;11(1):20462. doi: 10.1038/s41598-021-99182-3.
Influenza viruses cause severe respiratory infections in humans and birds, triggering global health concerns and economic burden. Influenza infection is a dynamic process involving complex biological host responses. The objective of this study was to illustrate global biological processes in ileum and cecal tonsils at early time points after chickens were infected with low pathogenic avian influenza virus (LPAIV) H9N2 through transcriptome analysis. Total RNA isolated from ileum and cecal tonsils of non-infected and infected layers at 12-, 24- and 72-h post-infection (hpi) was used for mRNA sequencing analyses to characterize differentially expressed genes and overrepresented pathways. Statistical analysis highlighted transcriptomic signatures significantly occurring 24 and 72 hpi, but not earlier at 12 hpi. Interferon (IFN)-inducible and IFN-stimulated gene (ISG) expression was increased, followed by continued expression of various heat-shock proteins (HSP), including HSP60, HSP70, HSP90 and HSP110. Some upregulated genes involved in innate antiviral responses included DDX60, MX1, RSAD2 and CMPK2. The ISG15 antiviral mechanism pathway was highly enriched in ileum and cecal tonsils at 24 hpi. Overall, most affected pathways were related to interferon production and the heat-shock response. Research on these candidate genes and pathways is warranted to decipher underlying mechanisms of immunity against LPAIV in chickens.
流感病毒可引起人类和鸟类的严重呼吸道感染,引发全球健康问题和经济负担。流感感染是一个涉及复杂生物宿主反应的动态过程。本研究的目的是通过转录组分析,阐明感染低致病性禽流感病毒(LPAIV)H9N2 后鸡早期回肠和盲肠扁桃体的全球生物学过程。使用来自非感染和感染层在感染后 12、24 和 72 小时(hpi)的回肠和盲肠扁桃体的总 RNA 进行 mRNA 测序分析,以表征差异表达基因和过表达途径。统计分析突出显示在 24 和 72 hpi 时发生的转录组特征,而在 12 hpi 时则不然。干扰素(IFN)诱导和 IFN 刺激基因(ISG)的表达增加,随后各种热休克蛋白(HSP)的持续表达,包括 HSP60、HSP70、HSP90 和 HSP110。一些参与先天抗病毒反应的上调基因包括 DDX60、MX1、RSAD2 和 CMPK2。ISG15 抗病毒机制途径在 24 hpi 时在回肠和盲肠扁桃体中高度富集。总的来说,受影响最大的途径与干扰素的产生和热休克反应有关。有必要对这些候选基因和途径进行研究,以阐明鸡对 LPAIV 免疫的潜在机制。