Literature DB >> 25100836

The Epstein-Barr virus (EBV) glycoprotein B cytoplasmic C-terminal tail domain regulates the energy requirement for EBV-induced membrane fusion.

Jia Chen1, Xianming Zhang2, Theodore S Jardetzky3, Richard Longnecker4.   

Abstract

The entry of enveloped viruses into host cells is preceded by membrane fusion, which in Epstein-Barr virus (EBV) is thought to be mediated by the refolding of glycoprotein B (gB) from a prefusion to a postfusion state. In our current studies, we characterized a gB C-terminal tail domain (CTD) mutant truncated at amino acid 843 (gB843). This truncation mutant is hyperfusogenic as monitored by syncytium formation and in a quantitative fusion assay and is dependent on gH/gL for fusion activity. gB843 can rescue the fusion function of other glycoprotein mutants that have null or decreased fusion activity in epithelial and B cells. In addition, gB843 requires less gp42 and gH/gL for fusion, and can function in fusion at a lower temperature than wild-type gB, indicating a lower energy requirement for fusion activation. Since a key step in fusion is the conversion of gB from a prefusion to an active postfusion state by gH/gL, gB843 may access this activated gB state more readily. Our studies indicate that the gB CTD may participate in the fusion function by maintaining gB in an inactive prefusion form prior to activation by receptor binding. Importance: Diseases resulting from Epstein-Barr virus (EBV) infection in humans range from the fairly benign disease infectious mononucleosis to life-threatening cancer. As an enveloped virus, EBV must fuse with a host cell membrane for entry and infection by using glycoproteins gH/gL, gB, and gp42. Among these glycoproteins, gB is thought to be the protein that executes fusion. To further characterize the function of the EBV gB cytoplasmic C-terminal tail domain (CTD) in fusion, we used a previously constructed CTD truncation mutant and studied its fusion activity in the context of other EBV glycoprotein mutants. From these studies, we find that the gB CTD regulates fusion by altering the energy requirements for the triggering of fusion mediated by gH/gL or gp42. Overall, our studies may lead to a better understanding of EBV fusion and entry, which may result in novel therapies that target the EBV entry step.
Copyright © 2014, American Society for Microbiology. All Rights Reserved.

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Year:  2014        PMID: 25100836      PMCID: PMC4178708          DOI: 10.1128/JVI.01349-14

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


  51 in total

1.  Fusion protein of the paramyxovirus SV5: destabilizing and stabilizing mutants of fusion activation.

Authors:  R G Paterson; C J Russell; R A Lamb
Journal:  Virology       Date:  2000-04-25       Impact factor: 3.616

2.  Structure of the Epstein-Barr virus gp42 protein bound to the MHC class II receptor HLA-DR1.

Authors:  Maureen M Mullen; Keith M Haan; Richard Longnecker; Theodore S Jardetzky
Journal:  Mol Cell       Date:  2002-02       Impact factor: 17.970

3.  Alternate replication in B cells and epithelial cells switches tropism of Epstein-Barr virus.

Authors:  Corina M Borza; Lindsey M Hutt-Fletcher
Journal:  Nat Med       Date:  2002-06       Impact factor: 53.440

4.  Activation of a paramyxovirus fusion protein is modulated by inside-out signaling from the cytoplasmic tail.

Authors:  David L Waning; Charles J Russell; Theodore S Jardetzky; Robert A Lamb
Journal:  Proc Natl Acad Sci U S A       Date:  2004-06-14       Impact factor: 11.205

5.  Fusion-deficient insertion mutants of herpes simplex virus type 1 glycoprotein B adopt the trimeric postfusion conformation.

Authors:  Jessica L Silverman; Sapna Sharma; Tina M Cairns; Ekaterina E Heldwein
Journal:  J Virol       Date:  2009-11-25       Impact factor: 5.103

6.  Fusion of epithelial cells by Epstein-Barr virus proteins is triggered by binding of viral glycoproteins gHgL to integrins alphavbeta6 or alphavbeta8.

Authors:  Liudmila S Chesnokova; Stephen L Nishimura; Lindsey M Hutt-Fletcher
Journal:  Proc Natl Acad Sci U S A       Date:  2009-11-17       Impact factor: 11.205

7.  Different functional domains in the cytoplasmic tail of glycoprotein B are involved in Epstein-Barr virus-induced membrane fusion.

Authors:  K M Haan; S K Lee; R Longnecker
Journal:  Virology       Date:  2001-11-10       Impact factor: 3.616

8.  Mutational analyses of Epstein-Barr virus glycoprotein 42 reveal functional domains not involved in receptor binding but required for membrane fusion.

Authors:  Amanda L Silva; Jasmina Omerovic; Theodore S Jardetzky; Richard Longnecker
Journal:  J Virol       Date:  2004-06       Impact factor: 5.103

9.  Mutations in the cytoplasmic domain of the Newcastle disease virus fusion protein confer hyperfusogenic phenotypes modulating viral replication and pathogenicity.

Authors:  Sweety Samal; Sunil K Khattar; Anandan Paldurai; Senthilkumar Palaniyandi; Xiaoping Zhu; Peter L Collins; Siba K Samal
Journal:  J Virol       Date:  2013-07-10       Impact factor: 5.103

10.  Structure of a trimeric variant of the Epstein-Barr virus glycoprotein B.

Authors:  Marija Backovic; Richard Longnecker; Theodore S Jardetzky
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-05       Impact factor: 11.205

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  10 in total

1.  Mutations in Pseudorabies Virus Glycoproteins gB, gD, and gH Functionally Compensate for the Absence of gL.

Authors:  Christina Schröter; Melina Vallbracht; Jan Altenschmidt; Sabrina Kargoll; Walter Fuchs; Barbara G Klupp; Thomas C Mettenleiter
Journal:  J Virol       Date:  2015-12-09       Impact factor: 5.103

2.  Epstein-Barr Virus Fusion with Epithelial Cells Triggered by gB Is Restricted by a gL Glycosylation Site.

Authors:  Britta S Möhl; Jia Chen; Seo Jin Park; Theodore S Jardetzky; Richard Longnecker
Journal:  J Virol       Date:  2017-11-14       Impact factor: 5.103

3.  The Glycoprotein B Cytoplasmic Domain Lysine Cluster Is Critical for Varicella-Zoster Virus Cell-Cell Fusion Regulation and Infection.

Authors:  Edward Yang; Ann M Arvin; Stefan L Oliver
Journal:  J Virol       Date:  2016-12-16       Impact factor: 5.103

4.  Interplay between the Herpes Simplex Virus 1 gB Cytodomain and the gH Cytotail during Cell-Cell Fusion.

Authors:  Henry B Rogalin; Ekaterina E Heldwein
Journal:  J Virol       Date:  2015-09-23       Impact factor: 5.103

5.  Epithelial cell infection by Epstein-Barr virus.

Authors:  Jia Chen; Richard Longnecker
Journal:  FEMS Microbiol Rev       Date:  2019-11-01       Impact factor: 16.408

Review 6.  Herpesvirus gB: A Finely Tuned Fusion Machine.

Authors:  Rebecca S Cooper; Ekaterina E Heldwein
Journal:  Viruses       Date:  2015-12-11       Impact factor: 5.048

7.  The Cytoplasmic Tail Domain of Epstein-Barr Virus gH Regulates Membrane Fusion Activity through Altering gH Binding to gp42 and Epithelial Cell Attachment.

Authors:  Jia Chen; Theodore S Jardetzky; Richard Longnecker
Journal:  MBio       Date:  2016-11-15       Impact factor: 7.867

8.  Immunoinformatic and systems biology approaches to predict and validate peptide vaccines against Epstein-Barr virus (EBV).

Authors:  Arif Ali; Abbas Khan; Aman Chandra Kaushik; Yanjie Wang; Syed Shujait Ali; Muhammad Junaid; Shoaib Saleem; William C S Cho; Xueying Mao; Dong-Qing Wei
Journal:  Sci Rep       Date:  2019-01-24       Impact factor: 4.379

Review 9.  Structural and Mechanistic Insights into the Tropism of Epstein-Barr Virus.

Authors:  Britta S Möhl; Jia Chen; Karthik Sathiyamoorthy; Theodore S Jardetzky; Richard Longnecker
Journal:  Mol Cells       Date:  2016-04-06       Impact factor: 5.034

10.  Structural basis for membrane anchoring and fusion regulation of the herpes simplex virus fusogen gB.

Authors:  Rebecca S Cooper; Elka R Georgieva; Peter P Borbat; Jack H Freed; Ekaterina E Heldwein
Journal:  Nat Struct Mol Biol       Date:  2018-05-04       Impact factor: 15.369

  10 in total

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