() infection is closely associated with the occurrence and development of gastric diseases. Therefore, eliminatinginfection should help to prevent gastric diseases. Vitamin D3 (VitD3, 1,25(OH)D) was previously observed to exhibit anti-infection activity in clinic, but these results were reported in heterogeneousstudies without elucidation of the underlying mechanisms. In the present study, we establishedinfection models in both wild-type and VDR knockdown (VDR) mice, which were used to demonstrate that VitD3 inhibitsinfection by enhancing the expression of VitD receptor (VDR) and cathelicidin antimicrobial peptide (CAMP). Furthermore, VDRmice that exhibited lower VDR expression were more susceptible toinfection. In cultured mouse primary gastric epithelial cells, we further demonstrated that the VitD3/VDR complex binds to the CAMP promoter region to increase its expression. These data provide a mechanistic explanation of the anti-infection activity of VitD3 at the molecular level in mice and suggest a new avenue for the clinical management oferadication therapy.