Ee. Haddad et al., EFFICACY OF A NOVEL INFECTIOUS BURSAL DISEASE VIRUS IMMUNE-COMPLEX VACCINE IN BROILER-CHICKENS, Avian diseases, 41(4), 1997, pp. 882-889
Two experiments were conducted to test the efficacy of a novel infecti
ous bursal disease virus (IBDV) vaccine in broiler chickens with mater
nal IBDV immunity. The IBDV vaccine was formulated by mixing IBDV stra
in 2512 with bursal disease antibodies (BDA) to produce the IBDV-BDA c
omplex vaccine. In Expt. I, 1-day-old Cobb x Cobb broiler chickens wer
e vaccinated subcutaneously with either IBDV-BDA or commercial live in
termediate IBDV vaccine (vaccine A) or were left unvaccinated. In Expt
. 2, the vaccine A group was not included; instead, IBDV strain 2512 w
as included. Chickens were maintained in isolation houses. On day 28 (
Expt. 1) and day 32 (Expt. 2) of age, chickens from each group were ch
allenged with a standard USDA IBDV (STC strain) challenge. Challenged
and unchallenged chickens were evaluated for their bursa/body weight r
atios and antibody titers 3 days post-challenge. Bursae collected from
Expt. 2 were examined histologically to evaluate bursal lesions and c
onfirm gross examination. None of the unvaccinated chickens was protec
ted against the challenge virus as evidenced by the presence of acute
bursal lesions (edema/hemorrhage). All chickens receiving the IBDV-BDA
complex or the IBDV strain 2512 (Expt. 2) were protected from the cha
llenge virus as evidenced by no acute bursal lesions. Additionally, ch
ickens receiving the IBDV-BDA complex vaccine or the IBDV strain 2512
had antibody titers to IBDV, indicating the presence of an active immu
ne response. In Expt. 1, chickens vaccinated with vaccine A and challe
nged had bursal lesions similar to those observed in the unvaccinated,
challenged chickens. These chickens also showed no indication of acti
ve immunity against the virus. These results suggest that the 1-day-of
-age-administered IBDV-BDA complex vaccine can induce active immunity
and protection against a standard IBDV challenge in the face of variab
le levels of maternal IBDV immunity.