Key Laboratory of Jiangsu Preventive Veterinary Medicine, Key Laboratory for Avian Preventive Medicine, Ministry of Education, College of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu, China.
Jiangsu Co-innovation Centre for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou, Jiangsu, China.
J Virol. 2020 Nov 23;94(24). doi: 10.1128/JVI.01767-20.
Although astroviruses causes enteric diseases and encephalitis in humans and nephritis and hepatitis in poultry, astrovirus infection is thought to be self-limiting. However, little is known about its molecular mechanism. In this study, we found that a novel goose astrovirus (GAstV), GAstV-GD, and its open reading frame 2 (ORF2) could efficiently activate the innate immune response and induce a high level of OASL and The truncation assay for ORF2 further revealed that the P2 domain of ORF2 contributed to stimulating OASL, whereas the acidic C terminus of ORF2 attenuated such activation. Moreover, the overexpression and knockdown of OASL could efficiently restrict and promote the viral replication of GAstV-GD, respectively. Our data not only give novel insights for elucidating self-limiting infection by astrovirus but also provide virus and host targets for fighting against astroviruses. Astroviruses cause gastroenteritis and encephalitis in human, and nephritis, hepatitis, and gout disease in poultry. However, the host immune response activated by astrovirus is mostly unknown. Here, we found that a novel goose astrovirus, GAstV-GD, and its ORF2 protein could efficiently induce a high level of OASL and which could feed back to restrict the replication of GAstV-GD, revealing novel innate molecules triggered by astroviruses and highlighting that the ORF2 of GAstV-GD and OASL can be potential antiviral targets for astroviruses.
虽然星形病毒可引起人类的肠道疾病和脑炎以及家禽的肾炎和肝炎,但人们认为星形病毒感染是自限性的。然而,其分子机制知之甚少。在本研究中,我们发现一种新型鹅星形病毒(GAstV),GAstV-GD,及其开放阅读框 2(ORF2)可有效激活先天免疫反应,并诱导高水平的 OASL 和 ORF2 的截断分析进一步表明,ORF2 的 P2 结构域有助于刺激 OASL,而 ORF2 的酸性 C 端则减弱了这种激活。此外,OASL 的过表达和敲低可分别有效地限制和促进 GAstV-GD 的病毒复制。我们的数据不仅为阐明星形病毒的自限性感染提供了新的见解,还为对抗星形病毒提供了病毒和宿主靶标。星形病毒可引起人类的肠胃炎和脑炎,以及家禽的肾炎、肝炎和痛风病。然而,星形病毒激活的宿主免疫反应大多未知。在这里,我们发现一种新型鹅星形病毒 GAstV-GD 及其 ORF2 蛋白可有效诱导高水平的 OASL 和 ,这可反馈限制 GAstV-GD 的复制,揭示了星形病毒触发的新的先天分子,并强调了 GAstV-GD 的 ORF2 和 OASL 可以作为星形病毒的潜在抗病毒靶标。