Department of Infectious Diseases, College of Veterinary Medicine, Konkuk University, Gwangjin-gu, Seoul 05029, Korea.
Department of Food and Nutrition, College of Biotechnology and Natural Resources, Chung-Ang University, Anseong, Gyeonggi 17546, Korea.
Viruses. 2021 Jan 11;13(1):92. doi: 10.3390/v13010092.
Norovirus genogroup II (NoV GII) induces acute gastrointestinal food-borne illness in humans. Because gnotobiotic pigs can be infected with human norovirus (HuNoV) GII, they are frequently used to analyze the associated pathogenic mechanisms and immune responses, which remain poorly understood. Recently, mRNA sequencing analysis (RNA-Seq) has been used to identify cellular responses to viruses. In this study, we investigated the host immune response and possible mechanisms involved in virus evasion in the ileum of gnotobiotic pigs infected with HuNoV by RNA-Seq. HuNoV was detected in the feces, blood, and tissues of the jejunum, ileum, colon, mesenteric lymph node, and spleen of pigs infected with HuNoV. In analysis of mRNA sequencing, expression of anti-viral protein genes such as OAS1, MX1, and MX2 were largely decreased, whereas type I IFN was increased in pigs infected with HuNoV. In addition, expression of and associated anti-inflammatory cytokine genes such as was increased in HuNoV-infected pigs. Expression of genes related to natural killer (NK) cell cytotoxicity and CD8 T cell exhaustion was increased, whereas that of MHC class I genes was decreased. Expression profiles of selected genes were further confirmed by qRT-PCR and Western blot. These results suggest that infection with HuNoV induces NK cell-mediated cytotoxicity but suppresses type I IFN- and CD8 T cell-mediated antiviral responses.
诺如病毒基因群 II(NoV GII)可引起人类急性胃肠道食源性疾病。由于无菌猪可以感染人类诺如病毒(HuNoV)GII,因此它们经常被用于分析相关的发病机制和免疫反应,但这些机制仍知之甚少。最近,mRNA 测序分析(RNA-Seq)已被用于鉴定细胞对病毒的反应。在这项研究中,我们通过 RNA-Seq 研究了感染 HuNoV 的无菌猪回肠中宿主免疫反应和可能涉及病毒逃避的机制。HuNoV 可在感染 HuNoV 的猪的粪便、血液和空肠、回肠、结肠、肠系膜淋巴结和脾脏组织中检测到。在 mRNA 测序分析中,抗病毒蛋白基因(如 OAS1、MX1 和 MX2)的表达大量减少,而 HuNoV 感染的猪中 I 型 IFN 增加。此外,HuNoV 感染的猪中 及相关抗炎细胞因子基因的表达增加。与自然杀伤(NK)细胞细胞毒性和 CD8 T 细胞耗竭相关的基因表达增加,而 MHC Ⅰ类基因的表达减少。通过 qRT-PCR 和 Western blot 进一步证实了选定基因的表达谱。这些结果表明,HuNoV 感染诱导 NK 细胞介导的细胞毒性,但抑制 I 型 IFN 和 CD8 T 细胞介导的抗病毒反应。