Effect of in vitro and in vivo 25-hydroxyvitamin D treatment on macrophages, T cells, and layer chickens during a coccidia challenge

被引:39
作者
Morris, A. [1 ]
Shanmugasundaram, R. [1 ]
McDonald, J. [1 ]
Selvaraj, R. K. [1 ]
机构
[1] Ohio State Univ, Ohio Agr Res & Dev Ctr, Dept Anim Sci, Wooster, OH 44691 USA
关键词
25-hydroxyvitamin D; coccidiosis; HD11; cells; layer chicken; T cells; NITRIC-OXIDE PRODUCTION; 1,25-DIHYDROXYVITAMIN D-3; INFECTION; LIPOPOLYSACCHARIDE; PERFORMANCE; INJECTION; SUPPLEMENTATION; GROWTH;
D O I
10.2527/jas.2014-8866
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
This article describes the in vitro and in vivo effects of a 25-hydroxycholecalciferol (25[OH] D) treatment in layer hens during a mixed coccidia challenge. HD11 cells (chicken macrophage cell line) were treated in vitro with a coccidia antigen or in a medium supplemented with either 1,25-dihydroxycholecalciferol (1,25[OH](2)D) or 25(OH)D. HD11 cells treated in vitro with 200 nM of 1,25(OH)(2)D had increased nitrite production (P < 0.01) compared with HD11 cells treated with 0 or 200 nM of 25(OH)D. Treating HD11 cells with 25(OH)D decreased IL-10 mRNA by 1.7-fold, but 1,25(OH)(2)D treatment increased the amount of IL-10 mRNA by 2.7-fold (P < 0.01) compared with the group treated with 0 nM of 25(OH)D. Post-coccidial antigen stimulation, 25(OH)D or 1,25(OH)(2)D treatment decreased (P < 0.01) 1 alpha-hydroxylase mRNA amounts in HD11 cells. Stimulating primary T cells in vitro with Concanavalin A (Con-A) decreased (P = 0.020) the 1 alpha-hydroxylase mRNA amounts by 3-fold. ConA-B1-VICK cells (chicken T cell line) stimulated with 100 nM 1,25(OH)(2)D or with supernatants from HD11 cells treated with 25(OH)D plus lipopolysaccharide (LPS) had 1.3-fold less (P < 0.01) interferon (IFN)-gamma mRNA compared with the group treated with 25(OH)D. Layer birds were fed a basal diet supplemented with 25(OH)D at 6.25, 25, 50, or 100 mu g/kg, and at 21 d of age orally challenged with 1 x 10(5) live coccidia oocysts. Compared with birds fed similar levels of 25(OH)D and unchallenged with the coccidia oocyst, birds challenged with the coccidia oocyst had 15% reduced BW gain in the groups supplemented with either 6.25, 25, or 50 mu g/kg of 25(OH)D, but only a 4% reduced BW gain in birds fed 100 mu g/kg of 25(OH)D (P < 0.01). Birds fed 100 mu g/kg 25(OH)D had decreased (P = 0.012) CD8+ cell percentages in cecal tonsils in both coccidial oocyst challenged and unchallenged birds, compared with birds fed 6.25 mu g/kg 25(OH) and unchallenged with coccidial oocysts. At 15 d post-coccidia challenge, birds fed 100 mu g/kg 25(OH)D and challenged with coccidial oocysts had 17% more CD4+CD25+ cells (P = 0.018) in the cecal tonsil compared with the birds fed 100 mu g/kg 25(OH)D and unchallenged with coccidial oocysts. At d 6 post-coccidia challenge, birds fed 100 mu g/kg 25(OH)D had a 3.5-fold increase (P < 0.01) in IL-10 mRNA amounts in the cecal tonsils compared with birds fed 6.25 mu g/kg 25(OH)D. In conclusion, supplementing birds with 100 mu g/kg 25(OH) D could be a nutritional strategy to reduce the production losses post-coccidia challenge.
引用
收藏
页码:2894 / 2903
页数:10
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