Cp. Czerny et al., A MONOCLONAL BLOCKING-ELISA FOR DETECTION OF ORTHOPOXVIRUS ANTIBODIESIN FELINE SERA, Veterinary microbiology, 52(3-4), 1996, pp. 185-200
A double sandwich blocking-ELISA using a genus-specific neutralizing m
onoclonal antibody (MAb) against the vaccinia virus 32 kD adsorption p
rotein (D8L open reading frame; ORF) was developed to detect orthopoxv
irus (OPV) antibodies in sera. A collection of 2173 feline serum sampl
es was examined in an epidemiological study. The blocking-ELISA reveal
ed 44 (2%) sera with positive titres of 1:2-1:256. ELISA results were
confirmed by the plaque-reduction test. A close correlation between ti
tres of both assays could be observed (r = 0.986). In general, the sen
sitivity of the blocking ELISA was two to four times higher. Neutraliz
ing OPV-antibodies were found in nine sera with ELISA-titres > 1:4. An
tibody specificity to OPV was also demonstrated by Western blotting an
alysis with selected feline sera. The epidemiographical distribution o
f the ELISA-positive sera and case histories of 37 seropositive cats a
vailable from the referring veterinarians are demonstrated. The blocki
ng-ELISA enables a rapid serological diagnosis and can be used in vete
rinary and human medicine. It allows OPV-antibody screening in human a
nd other animal species.