This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sharkey, C. M.
Right arrow Articles by Sanders, D. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sharkey, C. M.
Right arrow Articles by Sanders, D. A.

 Previous Article  |  Next Article 

Journal of Virology, March 2001, p. 2653-2659, Vol. 75, No. 6
0022-538X/01/$04.00+0   DOI: 10.1128/JVI.75.6.2653-2659.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Ross River Virus Glycoprotein-Pseudotyped Retroviruses and Stable Cell Lines for Their Production

C. Matthew Sharkey, Cynthia L. North, Richard J. Kuhn, and David Avram Sanders*

Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907-1392

Received 31 August 2000/Accepted 11 December 2000

Pseudotyped retroviruses have important applications as vectors for gene transfer and gene therapy and as tools for the study of viral glycoprotein function. Recombinant Moloney murine leukemia virus (Mo-MuLV)-based retrovirus particles efficiently incorporate the glycoproteins of the alphavirus Ross River virus (RRV) and utilize them for entry into cells. Stable cell lines that produce the RRV glycoprotein-pseudotyped retroviruses for prolonged periods of time have been constructed. The pseudotyped viruses have a broadened host range, can be concentrated to high titer, and mediate stable transduction of genes into cells. The RRV glycoprotein-pseudotyped retroviruses and the cells that produce them have been employed to demonstrate that RRV glycoprotein-mediated viral entry occurs through endocytosis and that membrane fusion requires acidic pH. Alphavirus glycoprotein-pseudotyped retroviruses have significant advantages as reagents for the study of the biochemistry and prevention of alphavirus entry and as preferred vectors for stable gene transfer and gene therapy protocols.


* Corresponding author. Mailing address: Department of Biological Sciences, Purdue University, 1392 Lilly Hall, West Lafayette, IN 47907. Phone: (765) 494-6453. Fax: (765) 496-1189. E-mail: retrovir{at}bragg.bio.purdue.edu.


Journal of Virology, March 2001, p. 2653-2659, Vol. 75, No. 6
0022-538X/01/$04.00+0   DOI: 10.1128/JVI.75.6.2653-2659.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Poluri, A., Ainsworth, R., Weaver, S. C., Sutton, R. E. (2008). Functional Pseudotyping of Human Immunodeficiency Virus Type 1 Vectors by Western Equine Encephalitis Virus Envelope Glycoprotein. J. Virol. 82: 12580-12584 [Abstract] [Full Text]  
  • Greenberg, K. P., Geller, S. F., Schaffer, D. V., Flannery, J. G. (2007). Targeted Transgene Expression in Muller Glia of Normal and Diseased Retinas Using Lentiviral Vectors. IOVS 48: 1844-1852 [Abstract] [Full Text]  
  • Strang, B. L., Takeuchi, Y., Relander, T., Richter, J., Bailey, R., Sanders, D. A., Collins, M. K. L., Ikeda, Y. (2005). Human Immunodeficiency Virus Type 1 Vectors with Alphavirus Envelope Glycoproteins Produced from Stable Packaging Cells. J. Virol. 79: 1765-1771 [Abstract] [Full Text]  
  • Kolokoltsov, A. A., Weaver, S. C., Davey, R. A. (2005). Efficient Functional Pseudotyping of Oncoretroviral and Lentiviral Vectors by Venezuelan Equine Encephalitis Virus Envelope Proteins. J. Virol. 79: 756-763 [Abstract] [Full Text]  
  • Kahl, C. A., Marsh, J., Fyffe, J., Sanders, D. A., Cornetta, K. (2004). Human Immunodeficiency Virus Type 1-Derived Lentivirus Vectors Pseudotyped with Envelope Glycoproteins Derived from Ross River Virus and Semliki Forest Virus. J. Virol. 78: 1421-1430 [Abstract] [Full Text]  
  • Inoue, N., Winter, J., Lal, R. B., Offermann, M. K., Koyano, S. (2003). Characterization of Entry Mechanisms of Human Herpesvirus 8 by Using an Rta-Dependent Reporter Cell Line. J. Virol. 77: 8147-8152 [Abstract] [Full Text]  
  • Jeffers, S. A., Sanders, D. A., Sanchez, A. (2002). Covalent Modifications of the Ebola Virus Glycoprotein. J. Virol. 76: 12463-12472 [Abstract] [Full Text]  
  • Kang, Y., Stein, C. S., Heth, J. A., Sinn, P. L., Penisten, A. K., Staber, P. D., Ratliff, K. L., Shen, H., Barker, C. K., Martins, I., Sharkey, C. M., Sanders, D. A., McCray, P. B. Jr., Davidson, B. L. (2002). In Vivo Gene Transfer Using a Nonprimate Lentiviral Vector Pseudotyped with Ross River Virus Glycoproteins. J. Virol. 76: 9378-9388 [Abstract] [Full Text]