J Gen Virol Try IJSEM Online
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 70 (1989), 1921-1927; DOI 10.1099/0022-1317-70-7-1921
© 1989 Society for General Microbiology

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Andersen, K. B.
Right arrow Articles by Skov, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Andersen, K. B.
Right arrow Articles by Skov, H.
Agricola
Right arrow Articles by Andersen, K. B.
Right arrow Articles by Skov, H.

Retrovirus-induced Cell Fusion Is Enhanced by Protease Treatment

Klaus B. Andersen and Helle Skov

Department of Biology, Danmarks farmaceutiske Højskole, Universitetsparken 2, DK-2100 København, Denmark

The effect of proteases on retrovirus-induced cell fusion was studied. Both ‘fusion from within’ (fusion between infected and uninfected cells) and ‘fusion from without’ (fusion of uninfected cells by virus addition) was enhanced after treatment with proteases. An enhancement of up to 10-fold, giving 30% fusion of the cells, was observed. Protease treatment of infected cells or of virus particles enhanced fusion, indicating that cleavage of the virus surface proteins is important for cell fusion. Cell fusion is believed to reflect the virus-cell membrane fusion which occurs during the entry of enveloped viruses into cells. It is therefore possible that proteolytic cleavage of virus surface components during entry is involved in virus infection.

Keywords: retrovirus, fusion, glycoprotein gp70

Received 29 February 1988; accepted 20 March 1989.


This article has been cited by other articles:


Home page
J. Virol.Home page
P. Kumar, D. Nachagari, C. Fields, J. Franks, and L. M. Albritton
Host Cell Cathepsins Potentiate Moloney Murine Leukemia Virus Infection
J. Virol., October 1, 2007; 81(19): 10506 - 10514.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
F. Diaz-Griffero, S. A. Hoschander, and J. Brojatsch
Endocytosis Is a Critical Step in Entry of Subgroup B Avian Leukosis Viruses
J. Virol., November 13, 2002; 76(24): 12866 - 12876.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
H. Moriuchi, M. Moriuchi, and A. S. Fauci
Cathepsin G, a Neutrophil-Derived Serine Protease, Increases Susceptibility of Macrophages to Acute Human Immunodeficiency Virus Type 1 Infection
J. Virol., August 1, 2000; 74(15): 6849 - 6855.
[Abstract] [Full Text]


Home page
J. Virol.Home page
J. L. Rohn, M. S. Moser, S. R. Gwynn, D. N. Baldwin, and J. Overbaugh
In Vivo Evolution of a Novel, Syncytium-Inducing and Cytopathic Feline Leukemia Virus Variant
J. Virol., April 1, 1998; 72(4): 2686 - 2696.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
S. Hwang, T. Boyle, H. Lyerly, and B. Cullen
Identification of the envelope V3 loop as the primary determinant of cell tropism in HIV-1
Science, July 5, 1991; 253(5015): 71 - 74.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1989 by the Society for General Microbiology.