作者
Qing Li,Hung Chan,Weixin Liu,Changan Liu,Yunfei Zhou,Dan Huang,Xueliang Wang,Xiaoxing Li,Chuan Xie,Wing Ying-Zhi Liu,Xiansong Wang,S. Ng,Hongyan Gou,Liuyang Zhao,Winnie Fong,Lanping Jiang,Yufeng Lin,Guijun Zhao,Feihu Bai,Xiaodong Liu,Huarong Chen,Lin Zhang,Sunny H. Wong,Matthew T.V. Chan,William Ka Kei Wu,Jun Yu
摘要
Carnobacterium maltaromaticum was found to be specifically depleted in female patients with colorectal cancer (CRC). Administration of C. maltaromaticum reduces intestinal tumor formation in two murine CRC models in a female-specific manner. Estrogen increases the attachment and colonization of C. maltaromaticum via increasing the colonic expression of SLC3A2 that binds to DD-CPase of this bacterium. Metabolomic and transcriptomic profiling unveils the increased gut abundance of vitamin D-related metabolites and the mucosal activation of vitamin D receptor (VDR) signaling in C. maltaromaticum-gavaged mice in a gut microbiome- and VDR-dependent manner. In vitro fermentation system confirms the metabolic cross-feeding of C. maltaromaticum with Faecalibacterium prausnitzii to convert C. maltaromaticum-produced 7-dehydrocholesterol into vitamin D for activating the host VDR signaling. Overall, C. maltaromaticum colonizes the gut in an estrogen-dependent manner and acts along with other microbes to augment the intestinal vitamin D production to activate the host VDR for suppressing CRC.