Nerbøvik I-K G, Solheim M A, Eggestøl H Ø, Rønneseth A, Jakobsen R A, Wergeland H I, Haugland G T
Department of Biology, Bergen High-Technology Centre, University of Bergen, Bergen, Norway.
J Fish Dis. 2017 Nov;40(11):1529-1544. doi: 10.1111/jfd.12622. Epub 2017 Apr 21.
The RIG-I receptors RIG-I, MDA5 and LGP2 are involved in viral recognition, and they have different ligand specificity and recognize different viruses. Activation of RIG-I-like receptors (RLRs) leads to production of cytokines essential for antiviral immunity. In fish, most research has focused on interferons, and less is known about the production of proinflammatory cytokines during viral infections. In this study, we have cloned the full-length MDA5 sequence in Atlantic salmon, and compared it with RIG-I and LGP2. Further, the salmonid cell line TO was infected with three fish pathogenic viruses, infectious pancreatic necrosis virus (IPNV), infectious salmon anaemia virus (ISAV) and salmonid alphavirus (SAV), and differential gene expression (DEG) analyses of RLRs, interferons (IFNa-d) and proinflammatory cytokines (TNF-α1, TNF-α2, IL-1β, IL-6, IL-12 p40s) were performed. The DEG analyses showed that the responses of proinflammatory cytokines in TO cells infected with IPNV and ISAV were profoundly different from SAV-infected cells. In the two aforementioned, TNF-α1 and TNF-α2 were highly upregulated, while in SAV-infected cells these cytokines were downregulated. Knowledge of virus recognition by the host and the immune responses during infection may help elucidate why and how some viruses can escape the immune system. Such knowledge is useful for the development of immune prophylactic measures.
视黄酸诱导基因I(RIG-I)样受体RIG-I、黑色素瘤分化相关基因5(MDA5)和实验室遗传学与生理学2(LGP2)参与病毒识别,它们具有不同的配体特异性,识别不同的病毒。RIG-I样受体(RLR)的激活导致产生抗病毒免疫所必需的细胞因子。在鱼类中,大多数研究集中在干扰素上,而关于病毒感染期间促炎细胞因子的产生了解较少。在本研究中,我们克隆了大西洋鲑鱼的全长MDA5序列,并将其与RIG-I和LGP2进行比较。此外,用三种鱼类致病性病毒,即传染性胰腺坏死病毒(IPNV)、传染性鲑鱼贫血病毒(ISAV)和鲑鱼α病毒(SAV)感染鲑鱼细胞系TO,并对RLR、干扰素(IFNa-d)和促炎细胞因子(肿瘤坏死因子-α1、肿瘤坏死因子-α2、白细胞介素-1β、白细胞介素-6、白细胞介素-12 p40s)进行差异基因表达(DEG)分析。DEG分析表明,感染IPNV和ISAV的TO细胞中促炎细胞因子的反应与感染SAV的细胞有很大不同。在上述两种情况中,肿瘤坏死因子-α1和肿瘤坏死因子-α2高度上调,而在感染SAV的细胞中这些细胞因子下调。了解宿主对病毒的识别以及感染期间的免疫反应可能有助于阐明为什么以及某些病毒如何能够逃避免疫系统。这些知识对于开发免疫预防措施很有用。