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Journal of Virology, January 2004, p. 531-538, Vol. 78, No. 1
0022-538X/04/$08.00+0     DOI: 10.1128/JVI.78.1.531-538.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Tetracycline-Inducible Packaging Cell Line for Production of Flavivirus Replicon Particles

Tracey J. Harvey,1,2 Wen Jun Liu,1,2 Xiang Ju Wang,1,2 Richard Linedale,1,2 Michael Jacobs,3 Andrew Davidson,4 Thuy T. T. Le,5 Itaru Anraku,5 Andreas Suhrbier,5 Pei-Yong Shi,6 and Alexander A. Khromykh1,2*

Sir Albert Sakzewski Virus Research Centre, Royal Children's Hospital,1 Clinical Medical Virology Centre, University of Queensland,2 Queensland Institute of Medical Research, Brisbane, Queensland, Australia,5 Centre for Hepatology, Royal Free & University College Medical School, London,3 Department of Pathology & Microbiology, School of Medical Sciences, Bristol, United Kingdom,4 Wadsworth Centre, New York State Department of Health, Albany, New York6

Received 18 June 2003/ Accepted 19 September 2003

We have previously developed replicon vectors derived from the Australian flavivirus Kunjin that have a unique noncytopathic nature and have been shown to direct prolonged high-level expression of encoded heterologous genes in vitro and in vivo and to induce strong and long-lasting immune responses to encoded immunogens in mice. To facilitate further applications of these vectors in the form of virus-like particles (VLPs), we have now generated a stable BHK packaging cell line, tetKUNCprME, carrying a Kunjin structural gene cassette under the control of a tetracycline-inducible promoter. Withdrawal of tetracycline from the medium resulted in production of Kunjin structural proteins that were capable of packaging transfected and self-amplified Kunjin replicon RNA into the secreted VLPs at titers of up to 1.6 x 109 VLPs per ml. Furthermore, secreted KUN replicon VLPs from tetKUNCprME cells could be harvested continuously for as long as 10 days after RNA transfection, producing a total yield of more than 1010 VLPs per 106 transfected cells. Passaging of VLPs on Vero cells or intracerebral injection into 2- to 4-day-old suckling mice illustrated the complete absence of any infectious Kunjin virus. tetKUNCprME cells were also capable of packaging replicon RNA from closely and distantly related flaviviruses, West Nile virus and dengue virus type 2, respectively. The utility of high-titer KUN replicon VLPs was demonstrated by showing increasing CD8+-T-cell responses to encoded foreign protein with increasing doses of KUN VLPs. A single dose of 2.5 x 107 VLPs carrying the human respiratory syncytial virus M2 gene induced 1,400 CD8 T cells per 106 splenocytes in an ex vivo gamma interferon enzyme-linked immunospot assay. The packaging cell line thus represents a significant advance in the development of the noncytopathic Kunjin virus replicon-based gene expression system and may be widely applicable to the basic studies of flavivirus RNA packaging and virus assembly as well as to the development of gene expression systems based on replicons from different flaviviruses.

* Corresponding author. Mailing address: Sir Albert Sakzewski Virus Research Centre, Royal Children's Hospital, Herston Road, Herston, QLD 4029, Australia. Phone: (617) 3253 3636. Fax: (617) 3636 1401. E-mail: a.khromykh{at}uq.edu.au.

Journal of Virology, January 2004, p. 531-538, Vol. 78, No. 1
0022-538X/04/$08.00+0     DOI: 10.1128/JVI.78.1.531-538.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.



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