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Journal of Virology, May 2000, p. 4394-4403, Vol. 74, No. 9
Sir Albert Sakzewski Virus Research Centre,
Royal Children's Hospital, Herston, Brisbane
4029,1 and Department of Microbiology
and Parasitology, University of Queensland, St. Lucia, Brisbane
4072,2 Australia
Received 13 December 1999/Accepted 11 February 2000
Primary features of the flavivirus Kunjin (KUN) subgenomic
replicons include continuous noncytopathic replication in host cell
cytoplasm and the ability to be encapsidated into secreted virus-like
particles (VLPs). Previously we reported preparation of RNA-based KUN
replicon vectors and expression of heterologous genes (HG) in cell
culture after RNA transfection or after infection with recombinant KUN
VLPs (A. N. Varnavski and A. A. Khromykh, Virology
255:366-375, 1999). In this study we describe the development of the
next generation of KUN replicon vectors, which allow synthesis of
replicon RNA in vivo from corresponding plasmid DNAs. These DNA-based
vectors were able to direct stable expression of
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Stable High-Level Expression of Heterologous Genes
In Vitro and In Vivo by Noncytopathic DNA-Based Kunjin Virus
Replicon Vectors
-galactosidase (
-Gal) in several mammalian cell lines, and expression remained high
(~150 pg per cell) throughout cell passaging. The applicability of
these vectors in vivo was demonstrated by
-Gal expression in the
mouse lung epithelium for at least 8 weeks after intranasal inoculation
and induction of anti-
-Gal antibody response after intramuscular
inoculation of the
-Gal-encoding KUN replicon DNA. The noncytopathic
nature of DNA-based KUN replicon vectors combined with high-level and
stability of HG expression in a broad range of host cells should prove
them to be useful in a variety of applications in vitro and in vivo.
*
Corresponding author. Mailing address: Sir Albert
Sakzewski Virus Research Centre, Royal Children's Hospital, Herston
Rd., Herston, Brisbane 4029, Australia. Phone: (617) 3253 1568. Fax: (617) 3253 1401. E-mail:
a.khromykh{at}mailbox.eq.edu.au.
Publication 104 from Sir Albert Sakzewski Virus Research Centre.
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