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 Zheng, C.
Right arrow Articles by van Drunen Littel-van den Hurk, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zheng, C.
Right arrow Articles by van Drunen Littel-van den Hurk, S.

 Previous Article  |  Next Article 

Journal of Virology, February 2005, p. 1948-1953, Vol. 79, No. 3
0022-538X/05/$08.00+0     doi:10.1128/JVI.79.3.1948-1953.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Bovine Herpesvirus 1 VP22 Enhances the Efficacy of a DNA Vaccine in Cattle{dagger}

Chunfu Zheng, Lorne A. Babiuk, and Sylvia van Drunen Littel-van den Hurk*

Vaccine and Infectious Disease Organization, University of Saskatchewan, Saskatoon, Saskatchewan, Canada

Received 7 April 2004/ Accepted 7 September 2004

For this study, the intercellular trafficking ability of bovine herpesvirus 1 (BHV-1) VP22 was applied to improve the efficacy of a DNA vaccine in calves. A plasmid encoding a truncated version of glycoprotein D (tgD) fused to VP22 was constructed. The plasmid encoding tgD-VP22 elicited significantly enhanced and more balanced immune responses than those induced by a plasmid encoding tgD. Furthermore, protection against a BHV-1 challenge was obtained in calves immunized with the plasmid encoding tgD-VP22, as shown by significant reductions in viral excretion. However, less significant protection was observed for animals vaccinated with the tgD-expressing plasmid, correlating with the lower level of immunity observed prechallenge. This is the first report of the use of VP22 as a transport molecule in the context of a DNA vaccine for a large animal species.


* Corresponding author. Mailing address: Vaccine and Infectious Disease Organization, University of Saskatchewan, 120 Veterinary Rd., Saskatoon, SK S7N 5E3, Canada. Phone: (306) 966-1559. Fax: (306) 966-7478. E-mail: vandenhurk{at}sask.usask.ca.

{dagger} VIDO's Journal Series number 370.


Journal of Virology, February 2005, p. 1948-1953, Vol. 79, No. 3
0022-538X/05/$08.00+0     doi:10.1128/JVI.79.3.1948-1953.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Yao, W., Liu, S., Qu, X., Xiao, S., Liu, Y., Liu, J. (2009). Enhanced immune response and protection efficacy of a DNA vaccine constructed by linkage of the Mycobacterium tuberculosis Ag85B-encoding gene with the BVP22-encoding gene. J Med Microbiol 58: 462-468 [Abstract] [Full Text]  
  • Zheng, C., Brownlie, R., Babiuk, L. A., van Drunen Littel-van den Hurk, S. (2005). Characterization of the Nuclear Localization and Nuclear Export Signals of Bovine Herpesvirus 1 VP22. J. Virol. 79: 11864-11872 [Abstract] [Full Text]