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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.

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.
Published ahead of print on 8 August 2007.
Present address: College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Ft. Collins, CO 80523.
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