Effects of 1,25-Dihydroxyvitamin D and 25-Hydroxyvitamin D on PBMCs From Dairy Cattle Naturally Infected With subsp. .

The role of vitamin D in modulating immune responses has been well-established for over two decades; however, its specific functions have not been extensively detailed in cattle, particularly cattle in different stages of infection with subspecies (MAP). Consistent with previous work in our lab, the present study showed that infected cattle in the clinical stage of disease have reduced serum 25-hydroxyvitamin D [25(OH)D]. Additionally, effects of vitamin D on peripheral blood mononuclear cells (PBMCs) from naturally infected dairy cattle in subclinical ( = 8) or clinical ( = 8) stages of infection were compared to non-infected control cows ( = 8). Briefly, PBMCs were isolated and cultured with 4 ng/ml 1,25-dihydroxyvitamin D [1,25(OH)D] or 100 ng/ml 25(OH)D. Treatment with 1,25(OH)D resulted in decreased secretion for some pro-inflammatory cytokines in clinical animals, including IL-1β, IL-6, and IFN-γ. Similar responses for IL-1β and IL-6 were noted with the addition of 25(OH)D. Additionally, pro-inflammatory cytokine gene expression tended to be upregulated in PBMCs from clinical animals after treatment with 1,25(OH)D. In contrast, PBMCs from clinical animals treated with 25(OH)D showed downregulation of pro-inflammatory cytokine gene expression, although only significant for . Following 25(OH)D treatment, clinical animals showed significant reduction in CD4+CD25+ T cells. gene expression was notably decreased in clinical and control animals following 25(OH)D treatment but increased in subclinical cows. 1,25(OH)D treatment reduced gene expression in all groups, while 25(OH)D treatment only significantly reduced expression for control cows. Lastly, serum 25(OH)D levels were significantly lower in clinical animals. Taken together, these data show vitamin D modulates cytokine signaling in cattle at different stages of MAP infection and, therefore, may have implications on disease progression.