Ten common kestrels (Falco tinnunculus) were used for this falcon herpes va
ccine experiment. Four kestrels were subcutaneously given 1 mi of an attenu
ated falcon herpesvirus that had originally been isolated from the liver of
an American prairie falcon (Falco mexicanus). This virus was then passaged
100 times on chicken embryo fibroblast cells (CEF-cells). Another 4 kestre
ls were given subcutaneously an inactivated falcon herpesvirus vaccine deri
ved from the same American field strain. This vaccine was concentrated, ina
ctivated by heat and betapropiolactone and emulsified in complete Freund's
adjuvans. Two further kestrels served as controls and were not vaccinated.
Twenty-one days after vaccination, all 10 kestrels were challenged with pas
sage 3 of the American falcon herpesvirus. The 2 control kestrels died 6 da
ys after challenge and 3 of those given the inactivated herpes vaccine died
9 days after challenge, with typical lesions of herpesvirus inclusion body
hepatitis. Before the vaccination experiment, all 10 kestrels were free of
serum neutralising antibodies to the falcon herpesvirus.
Twenty-one days after vaccination, all 4 kestrels vaccinated with the atten
uated vaccine, and one vaccinated with the killed vaccine, had seroconverte
d, having shown no symptoms to the challenge with a low passage virulent Am
erican herpesvirus strain. Following the challenge their antibody titres to
falcon herpesvirus increased. No herpesvirus was isolated from any of the
cloacal swabs taken during this experiment, indicating that there is no dan
ger for any other birds from the attenuated herpesvirus vaccine.
This experiment clearly shows that an attenuated falcon herpesvirus vaccine
can protect kestrels from fatal inclusion body hepatitis.