Literature DB >> 29959686

Stress Granule Formation is One of the Early Antiviral Mechanisms for Host Cells Against Coxsackievirus B Infection.

Xia Zhai1, Shuo Wu1, Lexun Lin1, Tianying Wang1, Xiaoyan Zhong1, Yang Chen1, Weizhen Xu1, Lei Tong1, Yan Wang1, Wenran Zhao2, Zhaohua Zhong3.   

Abstract

Stress granules (SGs) are intracellular granules formed when cellular translation is blocked and have been reported to be involved in a variety of viral infections. Our previous studies revealed that SGs are involved in the coxsackievirus B (CVB) infection process, but the role of SGs in CVB infection has not been fully explored. In this study, we found that CVB type 3 (CVB3) could induce SG formation in the early phase of infection. Results showed that levels of CVB3 RNA and protein were significantly inhibited during the early stage of CVB3 infection by the elevated formation of SGs, while viral RNA and protein synthesis were significantly promoted when SG formation was blocked. Our findings suggest that SG formation is one of the early antiviral mechanisms for host cells against CVB infection.

Entities:  

Keywords:  Coxsackievirus B (CVB); Stress granule (SG); Viral replication

Mesh:

Substances:

Year:  2018        PMID: 29959686      PMCID: PMC6178097          DOI: 10.1007/s12250-018-0040-3

Source DB:  PubMed          Journal:  Virol Sin        ISSN: 1995-820X            Impact factor:   4.327


  34 in total

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Authors:  K J Livak; T D Schmittgen
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2.  Poliovirus unlinks TIA1 aggregation and mRNA stress granule formation.

Authors:  James P White; Richard E Lloyd
Journal:  J Virol       Date:  2011-09-28       Impact factor: 5.103

3.  Modulation of hepatitis C virus RNA abundance and virus release by dispersion of processing bodies and enrichment of stress granules.

Authors:  Cara T Pager; Sylvia Schütz; Teresa M Abraham; Guangxiang Luo; Peter Sarnow
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4.  The NS1 protein of influenza A virus interacts with cellular processing bodies and stress granules through RNA-associated protein 55 (RAP55) during virus infection.

Authors:  Bobo Wing-Yee Mok; Wenjun Song; Pui Wang; Hung Tai; Yixin Chen; Min Zheng; Xi Wen; Siu-Ying Lau; Wai Lan Wu; Ken Matsumoto; Kwok-Yung Yuen; Honglin Chen
Journal:  J Virol       Date:  2012-09-12       Impact factor: 5.103

5.  Mammalian Orthoreovirus Factories Modulate Stress Granule Protein Localization by Interaction with G3BP1.

Authors:  Promisree Choudhury; Luke D Bussiere; Cathy L Miller
Journal:  J Virol       Date:  2017-10-13       Impact factor: 5.103

6.  Stable formation of compositionally unique stress granules in virus-infected cells.

Authors:  Joanna Piotrowska; Spencer J Hansen; Nogi Park; Katarzyna Jamka; Peter Sarnow; Kurt E Gustin
Journal:  J Virol       Date:  2010-01-27       Impact factor: 5.103

Review 7.  Regulation of stress granules in virus systems.

Authors:  James P White; Richard E Lloyd
Journal:  Trends Microbiol       Date:  2012-03-07       Impact factor: 17.079

8.  Zika virus inhibits eIF2α-dependent stress granule assembly.

Authors:  Raquel Amorim; Abdelkrim Temzi; Bryan D Griffin; Andrew J Mouland
Journal:  PLoS Negl Trop Dis       Date:  2017-07-17

9.  Coxsackievirus B3 inhibits antigen presentation in vivo, exerting a profound and selective effect on the MHC class I pathway.

Authors:  Christopher C Kemball; Stephanie Harkins; Jason K Whitmire; Claudia T Flynn; Ralph Feuer; J Lindsay Whitton
Journal:  PLoS Pathog       Date:  2009-10-16       Impact factor: 6.823

10.  Sequestration of G3BP coupled with efficient translation inhibits stress granules in Semliki Forest virus infection.

Authors:  Marc D Panas; Margus Varjak; Aleksei Lulla; Kai Er Eng; Andres Merits; Gunilla B Karlsson Hedestam; Gerald M McInerney
Journal:  Mol Biol Cell       Date:  2012-10-19       Impact factor: 4.138

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  4 in total

1.  Expression Profile and Function Analysis of Long Non-coding RNAs in the Infection of Coxsackievirus B3.

Authors:  Lei Tong; Ye Qiu; Hui Wang; Yunyue Qu; Yuanbo Zhao; Lexun Lin; Yan Wang; Weizhen Xu; Wenran Zhao; Hongyan He; Guangze Zhao; Mary H Zhang; Decheng Yang; Xingyi Ge; Zhaohua Zhong
Journal:  Virol Sin       Date:  2019-08-06       Impact factor: 4.327

Review 2.  The role of host eIF2α in viral infection.

Authors:  Yuanzhi Liu; Mingshu Wang; Anchun Cheng; Qiao Yang; Ying Wu; Renyong Jia; Mafeng Liu; Dekang Zhu; Shun Chen; Shaqiu Zhang; Xin-Xin Zhao; Juan Huang; Sai Mao; Xumin Ou; Qun Gao; Yin Wang; Zhiwen Xu; Zhengli Chen; Ling Zhu; Qihui Luo; Yunya Liu; Yanling Yu; Ling Zhang; Bin Tian; Leichang Pan; Mujeeb Ur Rehman; Xiaoyue Chen
Journal:  Virol J       Date:  2020-07-23       Impact factor: 4.099

Review 3.  Strategies for Success. Viral Infections and Membraneless Organelles.

Authors:  Aracelly Gaete-Argel; Chantal L Márquez; Gonzalo P Barriga; Ricardo Soto-Rifo; Fernando Valiente-Echeverría
Journal:  Front Cell Infect Microbiol       Date:  2019-10-11       Impact factor: 5.293

4.  The PERK/PKR-eIF2α Pathway Negatively Regulates Porcine Hemagglutinating Encephalomyelitis Virus Replication by Attenuating Global Protein Translation and Facilitating Stress Granule Formation.

Authors:  Junchao Shi; Zi Li; Rongyi Xu; Jing Zhang; Qianyu Zhou; Rui Gao; Huijun Lu; Yungang Lan; Kui Zhao; Hongbin He; Feng Gao; Wenqi He
Journal:  J Virol       Date:  2021-10-13       Impact factor: 5.103

  4 in total

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