Literature DB >> 24807724

Hijacking of host calreticulin is required for the white spot syndrome virus replication cycle.

Apiruck Watthanasurorot1, Enen Guo1, Sirinit Tharntada2, Chu-Fang Lo3, Kenneth Söderhäll4, Irene Söderhäll5.   

Abstract

We have previously shown that multifunctional calreticulin (CRT), which resides in the endoplasmic reticulum (ER) and is involved in ER-associated protein processing, responds to infection with white spot syndrome virus (WSSV) by increasing mRNA and protein expression and by forming a complex with gC1qR and thereby delaying apoptosis. Here, we show that CRT can directly interact with WSSV structural proteins, including VP15 and VP28, during an early stage of virus infection. The binding of VP28 with CRT does not promote WSSV entry, and CRT-VP15 interaction was detected in the viral genome in virally infected host cells and thus may have an effect on WSSV replication. Moreover, CRT was detected in the viral envelope of purified WSSV virions. CRT was also found to be of high importance for proper oligomerization of the viral structural proteins VP26 and VP28, and when CRT glycosylation was blocked with tunicamycin, a significant decrease in both viral replication and assembly was detected. Together, these findings suggest that CRT confers several advantages to WSSV, from the initial steps of WSSV infection to the assembly of virions. Therefore, CRT is required as a "vital factor" and is hijacked by WSSV for its replication cycle. Importance: White spot syndrome virus (WSSV) is a double-stranded DNA virus and the cause of a serious disease in a wide range of crustaceans that often leads to high mortality rates. We have previously shown that the protein calreticulin (CRT), which resides in the endoplasmic reticulum (ER) of the cell, is important in the host response to the virus. In this report, we show that the virus uses this host protein to enter the cell and to make the host produce new viral structural proteins. Through its interaction with two viral proteins, the virus "hijacks" host calreticulin and uses it for its own needs. These findings provide new insight into the interaction between a large DNA virus and the host protein CRT and may help in understanding the viral infection process in general.
Copyright © 2014, American Society for Microbiology. All Rights Reserved.

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Year:  2014        PMID: 24807724      PMCID: PMC4097763          DOI: 10.1128/JVI.01014-14

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  57 in total

1.  CRM1-dependent function of a cis-acting RNA export element.

Authors:  Ileana Popa; Matthew E Harris; John E Donello; Thomas J Hope
Journal:  Mol Cell Biol       Date:  2002-04       Impact factor: 4.272

2.  Cellular proteins from human monocytes bind to dengue 4 virus minus-strand 3' untranslated region RNA.

Authors:  Rosa Martha E Yocupicio-Monroy; Fernando Medina; Jorge Reyes-del Valle; Rosa M del Angel
Journal:  J Virol       Date:  2003-03       Impact factor: 5.103

3.  Proteins of purified Epstein-Barr virus.

Authors:  Eric Johannsen; Micah Luftig; Michael R Chase; Steve Weicksel; Ellen Cahir-McFarland; Diego Illanes; David Sarracino; Elliott Kieff
Journal:  Proc Natl Acad Sci U S A       Date:  2004-11-08       Impact factor: 11.205

4.  An ancient role for a prokineticin domain in invertebrate hematopoiesis.

Authors:  Irene Söderhäll; Young-A Kim; Pikul Jiravanichpaisal; So-Young Lee; Kenneth Söderhäll
Journal:  J Immunol       Date:  2005-05-15       Impact factor: 5.422

Review 5.  Plunder and stowaways: incorporation of cellular proteins by enveloped viruses.

Authors:  Réjean Cantin; Sylvie Méthot; Michel J Tremblay
Journal:  J Virol       Date:  2005-06       Impact factor: 5.103

6.  GRP78, a coreceptor for coxsackievirus A9, interacts with major histocompatibility complex class I molecules which mediate virus internalization.

Authors:  Kathy Triantafilou; Didier Fradelizi; Keith Wilson; Martha Triantafilou
Journal:  J Virol       Date:  2002-01       Impact factor: 5.103

7.  Involvement of endoplasmic reticulum chaperones in the folding of hepatitis C virus glycoproteins.

Authors:  A Choukhi; S Ung; C Wychowski; J Dubuisson
Journal:  J Virol       Date:  1998-05       Impact factor: 5.103

8.  Host and viral proteins in the virion of Kaposi's sarcoma-associated herpesvirus.

Authors:  Jill T Bechtel; Richard C Winant; Don Ganem
Journal:  J Virol       Date:  2005-04       Impact factor: 5.103

9.  Nucleocapsid protein VP15 is the basic DNA binding protein of white spot syndrome virus of shrimp.

Authors:  J Witteveldt; A M G Vermeesch; M Langenhof; A de Lang; J M Vlak; M C W van Hulten
Journal:  Arch Virol       Date:  2005-02-10       Impact factor: 2.574

10.  Contrasting functions of calreticulin and calnexin in glycoprotein folding and ER quality control.

Authors:  Maurizio Molinari; Klara Kristin Eriksson; Verena Calanca; Carmela Galli; Peter Cresswell; Marek Michalak; Ari Helenius
Journal:  Mol Cell       Date:  2004-01-16       Impact factor: 17.970

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  3 in total

1.  Regulation of Molecular Chaperone GRP78 by Hepatitis B Virus: Control of Viral Replication and Cell Survival.

Authors:  Wangqin Shu; Zhiwei Guo; Lijie Li; Zhiqi Xiong; Ziyu Wang; Yuanyuan Yang; Yuqi Li; Minjing He; Ruijie Gong; Bo Gao
Journal:  Mol Cell Biol       Date:  2020-01-16       Impact factor: 4.272

2.  Calreticulin modulates the intracellular survival of mycobacteria by regulating ER-stress-mediated apoptosis.

Authors:  Sung Hee Jo; Ji-Ae Choi; Yun-Ji Lim; Junghwan Lee; Soo-Na Cho; Sung-Man Oh; Dam Go; Seon-Hwa Kim; Chang-Hwa Song
Journal:  Oncotarget       Date:  2017-04-25

Review 3.  Molecular Mechanisms of White Spot Syndrome Virus Infection and Perspectives on Treatments.

Authors:  Bas Verbruggen; Lisa K Bickley; Ronny van Aerle; Kelly S Bateman; Grant D Stentiford; Eduarda M Santos; Charles R Tyler
Journal:  Viruses       Date:  2016-01-18       Impact factor: 5.048

  3 in total

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