Er. Jusa et al., HEMAGGLUTINATION WITH PORCINE REPRODUCTIVE AND RESPIRATORY SYNDROME VIRUS, Journal of veterinary medical science, 58(6), 1996, pp. 521-527
Porcine reproductive and respiratory syndrome (PRRS) virus grown on MA
RC-145 cell cultures was tested for hemagglutination (HA) with erythro
cytes from a variety of species at 4 degrees C, room temperature and 3
7 degrees C. HA was observed at all temperatures with mouse erythrocyt
es but not with cattle, sheep, goat, horse, swine, guinea pig, mongoli
an gerbil, goose and chicken erythrocytes. The HA activity was enhance
d by treatment of virus materials with Tween 80 followed by treatment
with ether. The HA titer and HA pattern of virus materials treated wit
h Tween 80 and ether (TE) were 4- to 8-fold higher and more clear than
those of the virus materials without TE treatment. The optimum condit
ions consisted in pretreatment of virus material with Tween 80 at a fi
nal concentration of 0.06-0.125% (v/v) for 15-60 min followed by treat
ment with ether at a concentration of 50% (v/v) for 5-15 min in ice ba
th with continuous shaking. The curve of active virus production in in
tra- and extracellular virus samples resembled that of HA production a
lthough it rose somewhat earlier in intracellular virus samples. The H
A reaction was inhibited by specific antiserum. HI antibody titers of
individual pig sera showed a significant positive correlation with the
ir neutralizing antibody titers.