Literature DB >> 24114795

Regulated IRE1-dependent decay pathway is activated during Japanese encephalitis virus-induced unfolded protein response and benefits viral replication.

Sankar Bhattacharyya1, Utsav Sen1, Sudhanshu Vrati1.   

Abstract

Japanese encephalitis virus (JEV) infection-induced encephalitis causes extensive death or long-term neurological damage, especially among children, in south and south-east Asia. Infection of mammalian cells has shown induction of an unfolded protein response (UPR), presumably leading to programmed cell death or apoptosis of the host cells. UPR, a cellular response to accumulation of unfolded or misfolded proteins in the endoplasmic reticulum (ER) lumen, is initiated by three ER-lumen-resident sensors (PERK, IRE1 and ATF6), and involves transcriptional and translational regulation of the expression of several genes. The sensor IRE1 possesses an intrinsic RNase activity, activated through homo-dimerization and autophosphorylation during UPR. Activated IRE1 performs cytoplasmic cleavage of Xbp1u transcripts, thus facilitating synthesis of XBP1S transcription factor, in addition to cleavage of a cohort of cellular transcripts, the later initiating the regulated IRE1-dependent decay (RIDD) pathway. In this study, we report the initiation of the RIDD pathway in JEV-infected mouse neuroblastoma cells (Neuro2a) and its effect on viral infection. Activation of the RIDD pathway led to degradation of known mouse cell target transcripts without showing any effect on JEV RNA despite the fact that both when biochemically purified showed significant enrichment in ER membrane-enriched fractions. Additionally, inhibition of the IRE1 RNase activity by STF083010, a specific drug, diminished viral protein levels and reduced the titre of the virus produced from infected Neuro2a cells. The results present evidence for the first report of a beneficial effect of RIDD activation on the viral life cycle.

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Year:  2013        PMID: 24114795     DOI: 10.1099/vir.0.057265-0

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  39 in total

1.  Japanese encephalitis virus replication is negatively regulated by autophagy and occurs on LC3-I- and EDEM1-containing membranes.

Authors:  Manish Sharma; Sankar Bhattacharyya; Minu Nain; Manpreet Kaur; Vikas Sood; Vishal Gupta; Renu Khasa; Malik Z Abdin; Sudhanshu Vrati; Manjula Kalia
Journal:  Autophagy       Date:  2014-07-16       Impact factor: 16.016

Review 2.  Emerging functions of the unfolded protein response in immunity.

Authors:  Sophie Janssens; Bali Pulendran; Bart N Lambrecht
Journal:  Nat Immunol       Date:  2014-10       Impact factor: 25.606

3.  Japanese Encephalitis Virus Induces Apoptosis and Encephalitis by Activating the PERK Pathway.

Authors:  Qianruo Wang; Xiu Xin; Ting Wang; Yuxin Tang; Shanshan Li; Lingbao Kong; Jiawu Wan; Yangtao Ou; Zibing Yang; Qijia Yu; Liting Zhu; Yunli Guo; Yinsheng Wu; Zhen Ding; Yanni Zhang; Zishu Pan
Journal:  J Virol       Date:  2019-08-13       Impact factor: 5.103

4.  Zika Virus Hijacks Stress Granule Proteins and Modulates the Host Stress Response.

Authors:  Shangmei Hou; Anil Kumar; Zaikun Xu; Adriana M Airo; Iryna Stryapunina; Cheung Pang Wong; William Branton; Egor Tchesnokov; Matthias Götte; Christopher Power; Tom C Hobman
Journal:  J Virol       Date:  2017-07-27       Impact factor: 5.103

5.  GRP78 Is an Important Host Factor for Japanese Encephalitis Virus Entry and Replication in Mammalian Cells.

Authors:  Minu Nain; Sriparna Mukherjee; Sonali Porey Karmakar; Adrienne W Paton; James C Paton; M Z Abdin; Anirban Basu; Manjula Kalia; Sudhanshu Vrati
Journal:  J Virol       Date:  2017-02-28       Impact factor: 5.103

6.  Duck Tembusu virus infection induces mitochondrial-mediated and death receptor-mediated apoptosis in duck embryo fibroblasts.

Authors:  Yuhong Pan; Wenjun Cai; Anchun Cheng; Mingshu Wang; Shun Chen; Juan Huang; Qiao Yang; Ying Wu; Di Sun; Sai Mao; Dekang Zhu; Mafeng Liu; Xinxin Zhao; Shaqiu Zhang; Qun Gao; Xumin Ou; Bin Tian; Zhongqiong Yin; Renyong Jia
Journal:  Vet Res       Date:  2022-07-07       Impact factor: 3.829

7.  ATF6-Mediated Unfolded Protein Response Facilitates Adeno-associated Virus 2 (AAV2) Transduction by Releasing the Suppression of the AAV Receptor on Endoplasmic Reticulum Stress.

Authors:  Mengtian Cui; Qingfang Zhao; Jing Wang; Yang Si; Shan Cheng; Wei Ding
Journal:  J Virol       Date:  2021-12-01       Impact factor: 6.549

8.  Inositol-Requiring Enzyme 1α Promotes Zika Virus Infection through Regulation of Stearoyl Coenzyme A Desaturase 1-Mediated Lipid Metabolism.

Authors:  Yanxia Huang; Quanshi Lin; Zhiting Huo; Cancan Chen; Shili Zhou; Xiaocao Ma; Huixin Gao; Yuxia Lin; Xiaobo Li; Junfang He; Ping Zhang; Chao Liu
Journal:  J Virol       Date:  2020-11-09       Impact factor: 5.103

9.  The Coronavirus Transmissible Gastroenteritis Virus Evades the Type I Interferon Response through IRE1α-Mediated Manipulation of the MicroRNA miR-30a-5p/SOCS1/3 Axis.

Authors:  Yanlong Ma; Changlin Wang; Mei Xue; Fang Fu; Xin Zhang; Liang Li; Lingdan Yin; Wanhai Xu; Li Feng; Pinghuang Liu
Journal:  J Virol       Date:  2018-10-29       Impact factor: 5.103

Review 10.  The unfolded protein response in immunity and inflammation.

Authors:  Joep Grootjans; Arthur Kaser; Randal J Kaufman; Richard S Blumberg
Journal:  Nat Rev Immunol       Date:  2016-06-27       Impact factor: 53.106

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