| Literature DB >> 32967952 |
Dan Ren1,2,3, Tuofan Li1,2,3, Xinyu Zhang1,2,3, Xiaohui Yao1,2,3, Wei Gao1,2,3, Quan Xie1,2,3, Jianjun Zhang4, Hongxia Shao1,2,3, Zhimin Wan1,2,3, Aijian Qin1,2,3, Jianqiang Ye5,2,3.
Abstract
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 in vitro and in vivo 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.IMPORTANCE 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 in vitro and in vivo, 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.Entities:
Keywords: OASL; ORF2; antiviral activity; goose astrovirus; innate immunity
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Year: 2020 PMID: 32967952 PMCID: PMC7925180 DOI: 10.1128/JVI.01767-20
Source DB: PubMed Journal: J Virol ISSN: 0022-538X Impact factor: 5.103