Study of the safety and efficacy of a recombinant vaccine for bluetongue virus serotype 2.

Vet Ital

Istituto Zooprofilattico Sperimentale dell'Abruzzo e del Molise G. Caporale, Via Campo Boario, 64100 Teramo, Italy.

Published: May 2010

AI Article Synopsis

  • A study vaccinated 7 cows, 10 sheep, and 10 goats with a recombinant vaccine for bluetongue virus serotype 2 (BTV-2), using both a normal dose (2.5 ml) and an increased dose (5 ml).
  • Following the vaccination, animals were monitored for antibody production, finding that while all showed c-ELISA antibodies, none developed neutralizing antibodies against BTV-2.
  • After a challenge with the virus, fever was noted in some vaccinated and control animals, but there were no major differences in blood chemical parameters among the groups.

Article Abstract

A total of 7 cows, 10 sheep and 10 goats were vaccinated subcutaneously with 5 ml of a recombinant vaccine consisting of synthetic virions containing the four principal proteins (VP2, VP3, VP5 and VP7) of bluetongue virus serotype 2 (BTV-2). The same number of animals and species were vaccinated with 2.5 ml (the normal vaccination dose) and 2 cows, 2 sheep and 2 goats were inoculated with a placebo and the adjuvant added to the vaccine. Animals vaccinated with the normal dose received a booster 14 days after the first injection and 8 sheep a third vaccination 4 months after the second inoculation. One month after the third vaccination, the 8 sheep and another 4 that had never come into contact with the virus were challenged with 1 ml of 10(5.8) TCID(50) of a BTV-2 Italian field isolate. All animals showed competitive enzyme-linked immunosorbent assay (c-ELISA) antibodies starting 14 days following the first vaccination. Conversely, no animal demonstrated neutralising antibodies to BTV-2 after vaccination. Fever (>40 degrees C) was observed in 6 vaccinated animals and 2 controls between 8 and 13 days post challenge. The virus was isolated from all animals from the 7th day post challenge. There was no significant difference in the blood chemical parameters tested and no significant interaction was found in the trial group.

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