Document Detail


Virus-like particle-induced fusion from without in tissue culture cells: role of outer-layer proteins VP4 and VP7.
MedLine Citation:
PMID:  9151849     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We recently described an assay that measures fusion from without induced in tissue culture cells by rotavirus, a nonenveloped, triple-protein-layered member of the Reoviridae family (M. M. Falconer, J. M. Gilbert, A. M. Roper, H. B. Greenberg, and J. S. Gavora, J. Virol. 69:5582-5591, 1995). The conditions required for syncytium formation are similar to those for viral penetration of the plasma membrane during the course of viral infection of host cells, as the presence of the outer-layer proteins VP4 and VP7 and the cleavage of VP4 are required. Here we present evidence that virus-like particles (VLPs) produced in Spodoptera frugiperda Sf-9 cells from recombinant baculoviruses expressing the four structural proteins of rotavirus can induce cell-cell fusion to the same extent as native rotavirus. This VLP-mediated fusion activity was dependent on trypsinization of VP4, and the strain-specific phenotype of individual VP4 molecules was retained in the syncytium assay similar to what has been seen with reassortant rotaviruses. We show that intact rotavirus and VLPs induce syncytia with cells that are permissive to rotavirus infection whereas nonpermissive cells are refractory to syncytium formation. This finding further supports our hypothesis that the syncytium assay accurately reflects very early events involved in viral infection and specifically the events related to viral entry into the cell. Our results also demonstrate that neither viral replication nor rotavirus proteins other than VP2, VP6, VP4, and VP7 are required for fusion and that both VP4 and VP7 are essential. The combination of a cell-cell fusion assay and the availability of recombinant VLPs will permit us to dissect the mechanisms of rotavirus penetration into host cells.
Authors:
J M Gilbert; H B Greenberg
Related Documents :
19876379 - Tipping the balance: robustness of tip cell selection, migration and fusion in angiogen...
21187919 - Magnetic fe₃o₄ nanoparticles and chemotherapy agents interact synergistically to in...
15745639 - Comparison of neurosphere cells with cumulus cells after fusion with embryonic stem cel...
2580919 - Adsorption of poly ri:rc on cell membrane participating and nonparticipating in interfe...
15908019 - Spinoculation of heparan sulfate deficient cells enhances hsv-1 entry, but does not abo...
8939659 - Adams and cell fusion.
17913889 - Z-ring force and cell shape during division in rod-like bacteria.
21104339 - Bioreduction of cu(ii) by cell-free copper reductase from a copper resistant pseudomona...
22933509 - Microfluidics for manipulating cells.
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Journal of virology     Volume:  71     ISSN:  0022-538X     ISO Abbreviation:  J. Virol.     Publication Date:  1997 Jun 
Date Detail:
Created Date:  1997-06-09     Completed Date:  1997-06-09     Revised Date:  2010-09-13    
Medline Journal Info:
Nlm Unique ID:  0113724     Medline TA:  J Virol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  4555-63     Citation Subset:  IM    
Affiliation:
Department of Microbiology and Immunology, Stanford University School of Medicine, California 94305, USA. jgilbert@apollo.stanford.edu
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Antigens, Viral*
Baculoviridae / genetics
Capsid / physiology*
Capsid Proteins*
Cell Fusion*
Cell Line
Cercopithecus aethiops
L Cells (Cell Line)
Membrane Fusion
Mice
Receptors, Virus / metabolism
Rotavirus / physiology*
Spodoptera
Grant Support
ID/Acronym/Agency:
DK38707/DK/NIDDK NIH HHS; R37AI21632/AI/NIAID NIH HHS; T32AI07328-08/AI/NIAID NIH HHS
Chemical
Reg. No./Substance:
0/Antigens, Viral; 0/Capsid Proteins; 0/Receptors, Virus; 0/VP4 protein, Rotavirus; 0/VP7 protein, Rotavirus
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Efficient encapsidation of human immunodeficiency virus type 1 vectors and further characterization ...
Next Document:  The amphotropic murine leukemia virus receptor gene encodes a 71-kilodalton protein that is induced ...