Penn State Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, Pennsylvania State University, University Park, PA, United States.
Applied Biological and Biosecurity Research Laboratory, Pennsylvania State University, University Park, PA, United States.
Front Cell Infect Microbiol. 2020 May 19;10:230. doi: 10.3389/fcimb.2020.00230. eCollection 2020.
Avian influenza viruses (AIVs) cause major economic losses to the global poultry industry. Many host factors have been identified that act as regulators of the inflammatory response and virus replication in influenza A virus (IAV) infected cells including nucleotide-binding oligomerization domain (NOD) like receptor (NLR) family proteins. Evidence is emerging that NLRC5, the largest NLR member, is a regulator of host immune responses against invading pathogens including viruses; however, its role in the avian immune system and AIV pathogenesis has not been fully explored. In this study, we found that NLRC5 is activated by a range of low and highly pathogenic AIVs in primary chicken lung cells and a chicken macrophage cell line. Further, siRNA mediated NLRC5 knockdown in chicken macrophages resulted in a significant reduction in AIV replication which was associated with the upregulation of genes associated with activated NFκB signaling pathway. The knockdown of NLRC5 enhanced the expression of genes known to be associated with viral defense and decreased innate cytokine gene expression following AIV infection. Overall, our investigation strongly suggests that NLRC5 is a pro-viral factor during IAV infection in chicken and may contribute to pathogenesis through innate cytokine regulation. Further studies are warranted to investigate the IAV protein(s) that may regulate activation of NLRC5.
禽流感病毒(AIVs)给全球家禽业造成了重大经济损失。许多宿主因素已被确定,它们作为流感 A 病毒(IAV)感染细胞中炎症反应和病毒复制的调节剂,包括核苷酸结合寡聚化结构域(NOD)样受体(NLR)家族蛋白。有证据表明,最大的 NLR 成员 NLRC5 是宿主对包括病毒在内的入侵病原体的免疫反应的调节剂;然而,其在禽类免疫系统和 AIV 发病机制中的作用尚未得到充分探索。在这项研究中,我们发现 NLRC5 被一系列低致病性和高致病性 AIV 在原代鸡肺细胞和鸡巨噬细胞系中激活。此外,鸡巨噬细胞中 NLRC5 的 siRNA 介导敲低导致 AIV 复制显著减少,这与激活 NFκB 信号通路相关基因的上调有关。NLRC5 的敲低增强了与病毒防御相关的基因的表达,并在 AIV 感染后降低了固有细胞因子基因的表达。总的来说,我们的研究强烈表明,NLRC5 是鸡中 IAV 感染的促病毒因子,可能通过先天细胞因子调节而导致发病机制。需要进一步的研究来调查可能调节 NLRC5 激活的 IAV 蛋白。