Jd. Moreau et al., ACTIVE IMMUNIZATION OF JAPANESE-QUAIL HENS WITH A RECOMBINANT CHICKENINHIBIN FUSION PROTEIN ENHANCES PRODUCTION PERFORMANCE, Poultry science, 77(6), 1998, pp. 894-901
The effects of active immunization against inhibin on production perfo
rmance in female Japanese quail (Coturnix coturnix japonica) were asse
ssed in two separate trials using an MBP-cINA521 fusion protein as an
immunogen. The fusion protein, MBP-cINA521, consisted of the bacterial
maltose binding protein (MBP) and a truncated form of the mature alph
a-subunit of chicken inhibin (cINA521). MBP-cINAI521 was constructed b
y: 1) excising a 521-bp PstI fragment from a chicken inhibin alpha-sub
unit cDNA (cINA6; gift of P. A. Johnson), 2) cloning this fragment, wh
ich encodes all but the first 11 amino acid residues of the mature alp
ha-subunit, into the pMal-c2 vector of the MBP fusion expression syste
m, and 3) expressing the fusion protein (MBP-cINA521) from the Escheri
chia coli and purifying it using affinity chromatography. In each tria
l, quail were randomly and equally assigned to one of two injection tr
eatments as follows: 1) MBP-cINA521 in Freund's adjuvant, or 2) Freund
's adjuvant (vehicular controls; CON). All immunizations were given su
bcutaneously and Freund's complete and incomplete adjuvant were used f
or primary and booster injections, respectively. In Trial 1, birds wer
e given a primary challenge of 0.2 mg MBP-cINA521 per bird at 25 d of
age, followed by booster immunizations (0.1 mg MBP-cINA521 per bird) a
t 33, 40, 47, 54 and 61 d of age and every 35 d thereafter. The CON bi
rds received vehicular immunizations at the same time intervals. In Tr
ial 2, birds treated with MBP-cINA521 received a primary challenge of
0.2 mg MBP-cINA521 per bird at 26 d of age, followed by booster immuni
zations (0.1 mg MBP-cINA521 per bird) using the same schedule as that
used in Trial 1, with the exception that no boosters were given after
61 d of age. The CON birds received vehicular immunizations at the sam
e time intervals. Collection of production performance data was initia
ted coincident with the laying of the first egg in each trial (i.e., b
eginning at 41 and 44 d of age for Trials 1 and 2, respectively) and c
ontinued for 30 l-wk periods of lay. Combined data from Trials 1 and 2
indicated that the mean + SE age at first egg lay was markedly decrea
sed (P < 0.005) in MBP-cINA521-treated quail (53.4 +/- 0.9 d of age) w
hen compared to the CON (57.6 +/- 1.3 d of age). Likewise, the mean +/
- SE age at 50% egg production was reduced (P < 0.03) in quail immuniz
ed against inhibin (65.4 +/- 2.1 d of age) when compared to the CON (7
7.6 +/- 9.7 d of age). Total hen-day egg production was also higher (P
< 0.05, Trial 1; P < 0.01, Trial 2) in MBP-cINA521-treated quail (88.
7 +/- 1.4%, Trial 1; 90.1 +/- 1.2%, Trial 2) than in the CON birds (81
.9 +/- 2.9%, Trial 1; 73.6 +/- 6.5%, Trial 2). Collectively, these fin
dings provide evidence that inhibin immunoneutralization accelerated p
uberty and enhanced hen-day egg production during a 30-wk period of eg
g lay in Japanese quail.