J Gen Virol Tips for Better Browsing
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Published online ahead of print on 4 March 2009 as doi:10.1099/vir.0.009019-0
Journal of General Virology 2009;90:1135.

A more recent version of this article appeared on May 1, 2009 J Gen Virol (2009), DOI 10.1099/vir.0.009019-0
© 2009 Society for General Microbiology

This Article
Right arrow Full Text (Papers in Press[PDF])
Right arrow All Versions of this Article:
vir.0.009019-0v1
90/5/1135    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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 CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wu, K.
Right arrow Articles by Kang, C. Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wu, K.
Right arrow Articles by Kang, C. Y.
Agricola
Right arrow Articles by Wu, K.
Right arrow Articles by Kang, C. Y.

Expression and processing of human immunodeficiency virus type 1 gp160 using the vesicular stomatitis virus New Jersey serotype vector system

Kunyu Wu1, Gyoung Nyoun Kim2 and C. Yong Kang2,3

1 University of Western Ontario;
2 The University of Western Ontario

3 E-mail: cykang{at}uwo.ca

The Indiana serotype of Vesicular Stomatitis Virus (VSVIND), but not the New Jersey serotype (VSVNJ), has been widely used as the gene expression vector. In terms of prime-boost based vaccine strategies, it would be desirable to use two different serotypes of VSV to avoid immunity against the priming viral vector. We report here that we applied VSVNJ vector system for expression of the env gene of human immunodeficiency virus type 1 (HIV-1). HIV-1 env gene was inserted into VSVNJ vector system at two different sites: between the P and M genes (NP-gp160-MGL) and between the G and L genes (NPMG-gp160-L). The HIV-1 env gene product, gp160, was efficiently expressed and processed in cells infected with either of these two recombinant VSV-HIV-1gp160 viruses. In this study, we have discussed the applicability of the VSVNJ vector system for foreign gene expression.

Received 21 November 2008; accepted 29 January 2009.





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2009 by the Society for General Microbiology.