Effects of dietary ratio of linoleic to linolenic acid on performance, antibody production, and in vitro lymphocyte proliferation in two strains of leghorn pullet chicks.

The effects of dietary ratio of linoleic acid to linolenic acid on performance, mitogenic lymphocyte proliferation, and antibody production were evaluated in Leghorn pullets during a rigorous vaccination program. Diets were supplemented with flaxseed and corn oil to achieve 4 dietary ratios of linoleic acid to linolenic acid [17:1 (control), 8:1, 4:1, or 2:1]. Each diet was fed to HyLine Brown or W-36 pullets from 1 d to 16 wk of age. Day-old pullets were randomly assigned to 8 replicate cages with 12 pullets per cage; the density was reduced to 8 pullets per cage at 11 wk of age. Dietary treatments did not affect body weight, feed consumption, or pullet mortality. At 12 wk of age, an interaction between diet and strain (P < or = 0.004) showed Hy-Line W-36 pullets fed the 2:1 ratio had greater antibody production against Newcastle disease virus (NDV) vaccine than those fed diets with higher ratios. At wk 16, pullets fed ratios of 4:1 and 2:1 had the greatest antibody production against NDV vaccine. Antibody production against infectious bursal disease virus (IBDV) vaccine was also increased (P < 0.04) by ratios of 4:1 (2.244 optical density; OD) or 2:1 (2.508 OD) as compared with the control diet (1.576 OD). Hy-Line Brown pullets had greater antibody production against infectious bronchitis virus vaccine compared with Hy-Line W-36 pullets at 16 wk of age. These results indicate that feeding a reduced dietary ratio of linoleic to linolenic acid by adding flaxseed to the diets enhanced antibody response to NDV and IBDV vaccines without any negative effects on pullet performance.

Effects of vitamin E and C supplementation on performance, in vitro lymphocyte proliferation, and antioxidant status of laying hens during heat stress.

Vitamin E (dl-alpha-tocopheryl acetate) was evaluated for its effects on performance, lymphocyte proliferation, and antioxidation in layers during heat stress. In Trial 1, 25, 45, or 65 IU of vitamin E/kg were fed to four replicated pens (five hens/cage) of DeKalb Delta or Hy-Line W-36 per treatment starting at 20 wk of age. At 34 wk of age, hens were heat-stressed at diurnal temperature ranging from 21 C to 35 C for 3 wk. The performances of hens not exposed to heat stress were not influenced by supplemental vitamin E. Supplemental vitamin E did not affect egg production; however, egg mass was greater (P < 0.05) with supplementation of 65 IU of vitamin E/ kg during heat stress. Egg yolk was significantly increased (P < 0.04) when hens were fed 45 and 65 lU/kg compared with the control vitamin E level (25 lU/kg). Haugh units were higher (P < 0.01) for hens fed 65 IU of vitamin E/kg compared to 25 and 45 lU/kg. Lymphocyte proliferative responses to concanavalin A (Con A) and Salmonella typhimurium lipopolysaccharide (LPS) were greater (P < 0.0001) in hens fed 45 and 65 IU of vitamin E/kg during heat stress. Strain had no effect on any of the parameters measured. In Trial 2, a 2 x 2 factorial was designed to test effects of vitamin C in drinking water (0 and 1,000 ppm) and dietary vitamin E (25 and 65 IU/kg). Eight replications per treatment with four hens per replication cage were heat-stressed at constant temperature of 35 C for 3 wk. Egg production and egg mass were higher when hens were fed 65 IU of vitamin E/kg than when hens were fed 25 lU/kg (81.5 vs. 75.9%, P < 0.03 and 48.2 vs. 44.6 g, P < 0.03, respectively). Yolk solids weight for the 65 IU vitamin E/kg group was higher (P < 0.01) compared to the 25 IU/kg group. ConA and LPS mitogenic responses were greater in hens fed 65 IU of vitamin E (P < 0.001 or P < 0.003, respectively) or 1,000 ppm of vitamin C (P < 0.001 or P < 0.002, respectively). The combination of 65 IU vitamin E/kg and 1,000 ppm vitamin C showed the highest ConA and LPS mitogenic responses among the treatments. No interaction effects of the two vitamins on production measurements or lymphocyte proliferative responses were observed. TBA values in egg yolk and plasma of hens fed 65 IU of vitamin E/kg were lower (P < 0.0001) than those of hens that received 25 IU of vitamin E/kg. These results suggest that vitamin E supplementation at 65 IU/kg diet may enhance production, induction of in vitro lymphocyte proliferation by ConA and LPS, and antioxidant properties of egg yolks and plasma of White Leghorn hens during heat stress and that supplementation of 1,000 ppm vitamin C may further enhance in vitro lymphocyte proliferative responses of hens during heat stress.