The unfolded protein response induced by Tembusu virus infection
文献类型: 外文期刊
第一作者: Zhao, Dongmin
作者: Zhao, Dongmin;Yang, Jing;Han, Kaikai;Liu, Qingtao;Liu, Yuzhuo;Huang, Xinmei;Zhang, Lijiao;Li, Yin;Zhao, Dongmin;Yang, Jing;Han, Kaikai;Liu, Qingtao;Liu, Yuzhuo;Huang, Xinmei;Zhang, Lijiao;Li, Yin;Wang, Huili
作者机构:
关键词: Tembusu virus; Endoplasmic reticulum stress; Unfolded protein response; Activation
期刊名称:BMC VETERINARY RESEARCH ( 影响因子:2.741; 五年影响因子:2.955 )
ISSN: 1746-6148
年卷期: 2019 年 15 卷
页码:
收录情况: SCI
摘要: BackgroundTembusu virus (TMUV), classified in the genus Flavivirus, causes reduced egg production and neurological problems in poultry. Flavivirus replication depends on the host endoplasmic reticulum (ER) and induces ER stress that leads to activation of the cellular unfolded protein response (UPR), an important signalling pathway that regulates many biological functions involved in viral pathogenesis and innate immunity. However, the mechanism of TMUV-induced UPR activation remains unclear.ResultsIn this study, we systematically investigated the three UPR pathways in TMUV-infected BHK-21 cells. Our results showed that expression of glucose-related protein 78 (GRP78) and GRP94 was upregulated during the course of TMUV infection. We then demonstrated that TMUV activated the PERK pathway in the early stage of infection, resulting in upregulation of ATF4, GADD34 and CHOP, with CHOP induction leading to caspase-3 activation. We also found the IRE1 pathway to be activated, leading to splicing of X box binding protein 1 (XBP1) mRNA and enhanced expression of p58(IPK). Finally, we observed increased expression of ATF6 and activity of ER stress-response elements, suggesting stimulation of the ATF6 pathway. In addition, ATF6 pathway activation correlated with the induction of downstream chaperones calnexin, calreticulin, ERp57 and PDI. UPR activity was also observed by the marked elevation in GRP78 and sXBP1 levels in TMUV-infected DF-1 cells.ConclusionsThis is the first report that TMUV infection-induced ER stress activates three branches of the UPR, and these results lay the foundation for elucidating the pathogenesis of TMUV and understanding the inherent mechanism of TMUV infection as well as the host response.
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