XBP1型
未折叠蛋白反应
ATF6
蛋白激酶R
生物
EIF-2激酶
ATF4
内质网
信号转导
细胞生物学
eIF2
冠状病毒
病毒复制
病毒学
激酶
蛋白激酶A
信使核糖核酸
核糖核酸
丝裂原活化蛋白激酶激酶
翻译(生物学)
病毒
基因
遗传学
医学
病理
2019年冠状病毒病(COVID-19)
细胞周期蛋白依赖激酶2
疾病
RNA剪接
传染病(医学专业)
作者
Puxian Fang,Liyuan Tian,Huichang Zhang,Sijin Xia,Tong Ding,Xuerui Zhu,Jian-Song Zhang,Jie Ren,Liurong Fang,Shaobo Xiao
标识
DOI:10.1016/j.vetmic.2022.109494
摘要
Porcine deltacoronavirus (PDCoV) is an emerging enteropathogenic coronavirus that has the potential for cross-species infection. Many viruses have been reported to induce endoplasmic reticulum stress (ERS) and activate the unfolded protein response (UPR). To date, little is known about whether and, if so, how the UPR is activated by PDCoV infection. Here, we investigated the activation state of UPR pathways and their effects on viral replication during PDCoV infection. We found that PDCoV infection induced ERS and activated all three known UPR pathways (inositol-requiring enzyme 1 [IRE1], activating transcription factor 6 [ATF6], and PKR-like ER kinase [PERK]), as demonstrated by IRE1-mediated XBP1 mRNA cleavage and increased mRNA expression of XBP1s, ATF4, CHOP, GADD34, GRP78, and GRP94, as well as phosphorylated eIF2α expression. Through pharmacologic treatment, RNA interference, and overexpression experiments, we confirmed the negative role of the PERK-eIF2α pathway and the positive regulatory role of the ATF6 pathway, but found no obvious effect of IRE1 pathway, on PDCoV replication. Taken together, our results characterize, for the first time, the state of the ERS response during PDCoV infection and identify the PERK and ATF6 pathways as potential antiviral targets.
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