猪流行性腹泻病毒
生物
未折叠蛋白反应
蛋白质生物合成
内质网
蛋白激酶R
翻译(生物学)
病毒学
病毒
eIF2
真核生物γ翻译起始因子4
细胞生物学
磷酸化
分子生物学
蛋白激酶A
遗传学
信使核糖核酸
细胞周期蛋白依赖激酶2
基因
作者
Liang Zheng,Ying Yang,Yifeng Han,Jiawen Yu,Zhijun Wu,Matthew Kay,Wenlong Xia,Zhibao Chen,Jinzhu Ma,Xiaoge Yang,Liwei Yin,Xiaojuan Xu,Hua Zhang
标识
DOI:10.1016/j.vetmic.2024.110095
摘要
Porcine epidemic diarrhea virus (PEDV) envelope protein (E) has been characterized as an important structural protein that plays critical roles in the interplay with its host to affect the virus life cycle. Stress granules (SGs) are host translationally silent ribonucleoproteins, which are mainly induced by the phosphorylation of eIF2α in the PERK/eIF2α signaling pathway. Our previous study found that PEDV E protein caused endoplasmic reticulum stress response (ERS)-mediated suppression of antiviral proteins' translation. However, the link and the underlying mechanism by which PEDV induces SGs formation and suppresses host translation remain elusive. In this study, our results showed that PEDV E protein significantly elevated the expression of GRP78, CANX, and phosphorylation of PERK and eIF2α, indicating that the PERK/eIF2α branch of ERS was activated. PEDV E protein localized to the ER and aggregated into puncta to reconstruct ER structure, and further induced SGs formation, which has been caused through upregulating the G3BP1 expression level. In addition, a significant global translational stall and endogenous protein translation attenuation were detected in the presence of E protein overexpression, but the global mRNA transcriptional level remained unchanged, suggesting that the shutoff of protein translation was associated with the translation, not with the transcription process. Collectively, this study demonstrates that PERK/eIF2α activation is required for SGs formation and protein translation stall. This study is beneficial for us to better understand the mechanism by which PEDV E suppresses host protein synthesis, and provides us a new insight into the host translation regulation during virus infection.
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