Ca. Hanlon et al., FIRST NORTH-AMERICAN FIELD RELEASE OF A VACCINIA-RABIES GLYCOPROTEIN RECOMBINANT VIRUS, Journal of wildlife diseases, 34(2), 1998, pp. 228-239
Following nearly 10 yr of extensive laboratory evaluation, a vaccinia-
rabies glycoprotein (V-RG) vaccine was the first recombinant virus to
undergo limited North American field release on 20 August 1990. The fr
ee-ranging raccoon population on Parramore Island (Virginia,, USA) was
exposed to a high density (10 baits/ha) of vaccine-laden baits distri
buted on a 300 ha vaccination area. Art annual total of 887 raccoons w
ere live-trapped for sedation, physical examination and blood collecti
on for rabies antibody determination: there was no evidence of adverse
effects or lesions due to the vaccine. Age and sex distributions, mea
n body weights, and live-capture histories of raccoons from the vaccin
ation and non-baited control areas were compared. There were no statis
tically significant differences in survivorship between the baited and
nonbaited areas, nor between rabies antibody-positive and antibody-ne
gative raccoons from the vaccination area. There was no trend in field
mortality that suggested an association with either tetracycline or s
ulfadimethoxine, used as biomakers, or with vaccine contact determined
by antibody status. No gross or histopathologic lesions due to the va
ccine were demonstrated among a subsample of live-trapped raccoons col
lected for gross necropsy, biomarker analysis, histopathologic examina
tion, and V-RG virus isolation attempts. Recovery of V-RG virus was li
mited to the tonsils of two biomarker-postitive, clinically healthy ra
ccoons collected from the vaccination area for postmortem examination
on days 2 and 4 following bait distribution. These data reinforce the
extensive body of safety data on the V-RG virus and extend it to inclu
de field evaluation where vaccine is offered free-choice in abundance,
in baits designed to attract free-ranging raccoons, in a relatively s
imple ecosystem.