ACTIVE IMMUNIZATION OF JAPANESE-QUAIL HENS WITH A RECOMBINANT CHICKENINHIBIN FUSION PROTEIN ENHANCES PRODUCTION PERFORMANCE

Citation
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
Citations number
38
Categorie Soggetti
Agriculture Dairy & AnumalScience
Journal title
ISSN journal
00325791
Volume
77
Issue
6
Year of publication
1998
Pages
894 - 901
Database
ISI
SICI code
0032-5791(1998)77:6<894:AIOJHW>2.0.ZU;2-L
Abstract
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.