Abstract |
Weaned pigs (6-week-old) and 7-day-old pre-weaned piglets were vaccinated with naked plasmid DNA expressing the gp55/E2 gene from classical swine fever virus (CSFV). Both groups of pigs were then given a booster dose of recombinant porcine adenovirus expressing the gp55 gene (rPAV-gp55). Following challenge with CSFV, 100% of weaned pigs and 75% pre-weaned piglets were protected from disease. Weaned pigs given a single dose of rPAV-gp55 were also protected, but showed a slight increase in temperature immediately post-challenge. However, weaned animals given a DNA prime before rPAV-gp55 showed no fluctuation in body temperature following challenge and no pathology in spleen or lymph nodes upon post-mortem. In addition, no CSFV could be re-isolated from the rPAV vaccinated group and from only one pig in the prime-boost group following challenge, suggesting that both vaccination regimes have the potential to reduce or prevent virus shedding following experimental challenge.
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Authors | J M Hammond, E S Jansen, C J Morrissy, W V Goff, G C Meehan, M M Williamson, C Lenghaus, K W Sproat, M E Andrew, B E Coupar, M A Johnson |
Journal | Veterinary microbiology
(Vet Microbiol)
Vol. 80
Issue 2
Pg. 101-19
(May 21 2001)
ISSN: 0378-1135 [Print] Netherlands |
PMID | 11295331
(Publication Type: Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- DNA, Recombinant
- Vaccines, DNA
- Viral Envelope Proteins
- glycoprotein E2, classical swine fever virus
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Topics |
- Adenoviridae
- Animals
- Body Temperature
- Classical Swine Fever
(prevention & control)
- DNA, Recombinant
(administration & dosage)
- Enzyme-Linked Immunosorbent Assay
(veterinary)
- Swine
- Vaccination
(veterinary)
- Vaccines, DNA
- Viral Envelope Proteins
(genetics, immunology)
- Weaning
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