猪繁殖与呼吸综合征病毒
基因敲除
生物
MDA5型
病毒学
干扰素
异位表达
病毒复制
动脉瘤
病毒
小干扰RNA
分子生物学
核糖核酸
细胞培养
基因
RNA干扰
医学
生物化学
2019年冠状病毒病(COVID-19)
病理
疾病
传染病(医学专业)
遗传学
作者
Mengmeng Zhao,Huiyang Sha,Huawei Li,Hang Zhang,Li Huang,Ruining Wang
标识
DOI:10.1016/j.intimp.2022.109151
摘要
Porcine reproductive and respiratory syndrome virus 2 (PRRSV-2) is a constant threat to the swine industry worldwide. 2', 5'-oligoadenylate synthetase-like (OASL) protein has antiviral activity, but this has not been demonstrated for PRRSV-2, and the mechanism is not well elucidated.In this study, the expression of OASL1 in porcine alveolar macrophages (PAMs) induced by interferon (IFN)-β stimulation and PRRSV-2 infection was examined by quantitative real-time polymerase chain reaction and western blotting. Ectopic expression and knockdown of porcine OASL1 (pOASL1) indicated the role of OASL1 in PRRSV-2 replication cycle. Results showed that the expression of OASL1 in PAMs was significantly increased by IFN-β stimulation or PRRSV-2 infection. OASL1 specific small interfering RNA promoted PRRSV-2 replication, whereas ectopic expression of pOASL1 inhibited PRRSV-2 infection. The mechanism revealed OASL1 interacts with Melanoma differentiation-associated protein 5 (MDA5) to increase IFN responses, and the anti-PRRSV-2 activity was lost after the knockdown of the MDA5 RNA sensor.OASL1 inhibits PRRSV-2 infection via the activation of MDA5.
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