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 Google Scholar
Google Scholar
Right arrow Articles by Seino, K. K.
Right arrow Articles by Bourgeois, M. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Seino, K. K.
Right arrow Articles by Bourgeois, M. A.
Right arrowPubmed/NCBI databases
Medline Plus Health Information
*West Nile Virus

 Previous Article  |  Next Article 

Clinical and Vaccine Immunology, November 2007, p. 1465-1471, Vol. 14, No. 11
1071-412X/07/$08.00+0     doi:10.1128/CVI.00249-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Comparative Efficacies of Three Commercially Available Vaccines against West Nile Virus (WNV) in a Short-Duration Challenge Trial Involving an Equine WNV Encephalitis Model{triangledown}

K. K. Seino,* M. T. Long, E. P. J. Gibbs, R. A. Bowen,{dagger} S. E. Beachboard, P. P. Humphrey, M. A. Dixon, and M. A. Bourgeois

College of Veterinary Medicine, University of Florida, 2015 SW 16th Avenue, Gainesville, Florida 32610

Received 19 June 2007/ Accepted 29 July 2007

We used a severe challenge model that produces clinical West Nile virus (WNV) disease to test the efficacy of three commercially available equine WNV vaccines in horses. Twenty-four healthy, WNV-seronegative horses of varying ages and genders were placed, in random and blind manner, into three trial groups consisting of eight horses each; two horses in each group received (i) an inactivated WNV vaccine (K-WN), (ii) a modified-live vaccine (CP-WN) containing the WNV prM and E proteins expressed by a canarypox vector, (iii) a live-chimera vaccine (WN-FV) containing WNV prM and E proteins expressed in a YF17D vector, or (iv) a diluent control. Challenge by this model caused grave neurological signs, viremia, moderate to severe histopathologic lesions in the brain and spinal cord, and an outcome of 0% survivorship in all six control horses. In contrast, challenge in horses at between 28 days postvaccination with the chimera vaccine and 56 days postvaccination with the commercial inactivated or modified-live vaccine resulted in 100% survivorship (protection from the onset of WNV encephalitis and viremia). Horses vaccinated with the live-chimera vaccine showed significantly fewer clinical signs than did the control horses (P ≤ 0.01) and the horses vaccinated with inactivated vaccine (P = 0.035). Mild residual inflammatory lesions were seen in a few of the vaccinated horses.


* Corresponding author. Mailing address: College of Veterinary Medicine, University of Florida, 2015 SW 16th Avenue, Gainesville, FL 32610. Phone: (352) 392-2212. Fax: (352) 392-5993. E-mail: seinok{at}mail.vetmed.ufl.edu

{triangledown} Published ahead of print on 8 August 2007.

{dagger} Present address: College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Ft. Collins, CO 80523.


Clinical and Vaccine Immunology, November 2007, p. 1465-1471, Vol. 14, No. 11
1071-412X/07/$08.00+0     doi:10.1128/CVI.00249-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.