Bangxin Xue, Fengju Liu, Jiale Bao, Shengjie Shi, Shuang Cai, Xiangzhou Zeng, Xinyu Wang, Zhekun Zhu, Guiyan Chu, Xiangfang Zeng, Shimin Liu, Peng Qin, Chuanjiang Cai, Zhenhua Xue
This study compared vitamin D3 with an equivalent supranutritional dose of chemically or microbially produced 25-OH-D3 from day 90 of gestation to weaning.
Vitamin D and its metabolite 25-hydroxyvitamin D3 (25-OH-D3) are central to calcium homeostasis, maternal skeletal integrity, and sow reproductive efficiency. This study compared vitamin D3 with an equivalent supranutritional dose of chemically or microbially produced 25-OH-D3 from day 90 of gestation to weaning. A total of 100 Large White × Landrace sows were assigned to five treatments (n = 20): a basal control (25 µg/kg vitamin D3), a VD3 group (basal + 50 µg/kg vitamin D3), and three 25-OH-D3 groups (basal + 50 µg/kg 25-OH-D3; QV1-QV3). Reproductive traits, colostrum composition, serum vitamin D-related indices, antioxidant and cytokine profiles, pre-weaning piglet growth, femoral mineral concentration, intestinal morphology, and barrier-related gene expression were assessed. Compared with the control, QV2 increased litter weight gain from birth to day 14 by 9.8%, piglet serum 25-OH-D3 at weaning by 33.2%, and femoral calcium concentration by 14.4% (p < 0.05); litter and average piglet weights at weaning were unchanged. Maternal 25-OH-D3 supplementation also altered the overall redox profile and several circulating inflammatory cytokines, increased jejunal and ileal villus height in the QV2 and QV3 groups, and upregulated selected tight-junction-related genes, including occludin and ZO-1, in a source- and intestinal-segment-dependent manner (p < 0.05). Responses were source-dependent, and QV2 showed the strongest effects for selected endpoints; the data do not support class-wide superiority of biosynthesized preparations.