Bile microbiome and metabolic characteristics in primary common bile duct stone patients with juxtapapillary duodenal diverticula: a clinical investigation

胃肠病学 内科学 医学 胆总管 微生物群 代谢活性 胆汁酸 肠道微生物群 肠球菌 链球菌科 微生物学 胆管 代谢途径 拟杆菌科 细菌 小学(天文学) 代谢紊乱 克雷伯菌 生物
作者
Mengying Wang,Hongtao Hou,Wei Sang,Pingping Li,Xuxu Yang,Ping Qi,Yu Ma,Yanmei Qui,Jian Zhang
出处
期刊:Journal of Applied Microbiology [Oxford University Press]
卷期号:137 (6) 被引量:1
标识
DOI:10.1093/jambio/lxaf280
摘要

OBJECTIVE: This study aimed to characterize the bile microbiome and metabolome in patients with common bile duct stones (CBDs), with versus without juxtapapillary duodenal diverticulum (JPDD), to identify potential factors associated with stone formation. METHODS: From January to May 2024, CBDs patients undergoing endoscopic retrograde cholangiopancreatography at our hospital were prospectively enrolled. Bile samples were collected for 16S rRNA sequencing and LC-MS/MS metabolomics analysis. Patients were divided into JPDD (n = 15) and CBDs (n = 15) groups. RESULTS: The JPDD group had larger stone and bile duct diameters (P < 0.05). Although Proteobacteria dominated the bile microbiota in both groups, the JPDD group showed higher abundances of Escherichia-Shigella, Enterococcus, and Escherichia coli. Beta diversity differed significantly between groups (P < 0.05), and LEfSe identified 25 differentially abundant bacterial taxa. Enterococcus, Klebsiella, and Gemellaceae were more abundant in the JPDD group, while Peptococcaceae, Roseburia, and Alistipes were more prevalent in the CBDs group. Enterococcaceae and Enterococcus abundances were positively correlated with stone and duct sizes in the JPDD group (P < 0.05), whereas Peptococcaceae and Acinetobacter showed negative correlations. Metabolomic analysis identified ten differentially enriched pathways-including phenylalanine and alanine metabolism-and higher levels of bilirubin glucuronide and taurochenodeoxycholic acid in the JPDD group. Enterococcus abundance was correlated with bile acid metabolites such as chenodeoxycholylasparagine (P < 0.05). CONCLUSIONS: JPDD is associated with distinct microbial and metabolic profiles in bile. Enrichment of Enterococcus and Klebsiella in the JPDD group, along with changes in metabolic pathways and bile acid metabolites, suggests a potential link to CBD stone formation and growth.
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