Zhao Yi, Dai Zhengqun, Lang Yanmei, Li Rui, Zheng Hongyu, Mi Jiajia, He Xiu, Liu Jin, Xiang Rong, Mei Xueran, Liu Yang, Wang Yantang, Guo Huijie, Yang Qian, Ren Ke, Yang Tai
School of Pharmacy, Chengdu Medical College, Sichuan Province, Chengdu, China.
Precision Medicine Center, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Probiotics Antimicrob Proteins. 2025 May 27. doi: 10.1007/s12602-025-10595-2.
Chemotherapy-induced diarrhea (CID) is a frequent gastrointestinal side effect in cancer patients, particularly associated with the use of 5-fluorouracil (5-FU). This study aimed to isolate multiple Bacteroides strains from the feces of healthy individuals and identify Bacteroides eggerthii (B. eggerthii) S13-F8 as the optimal candidate for alleviating CID. Whole-genome sequencing of B. eggerthii S13-F8 was conducted to uncover its functional characteristics and explore the potential mechanisms underlying its protective effects against CID. The anti-CID efficacy of B. eggerthii S13-F8 was assessed using multiple parameters, including diarrhea severity, food intake, and body weight changes. Comprehensive analyses, including blood tests, intestinal histopathology, colon transcriptomics, and fecal metagenomics, were performed to elucidate its underlying mechanisms. In a 5-FU-induced mouse model, B. eggerthii S13-F8 significantly alleviated weight loss and diarrhea. Histological examination revealed that B. eggerthii S13-F8 preserved the villus height-to-crypt depth (V/C) ratio and protected goblet cells in colonic tissues. Gene expression analysis showed that B. eggerthii S13-F8 upregulated protective markers, such as Aqp8, Slc26a3, and mucin-related genes (TFF3, FCGBP, and Muc2), while downregulating pro-inflammatory mediators, including IL-1α, IL-22, and Cxcl2. Furthermore, B. eggerthii S13-F8 modulated gut microbiota composition by suppressing pathogenic bacteria (Pseudomonas aeruginosa, Salmonella, γ-Proteobacteria, and Shigella) and enriching beneficial taxa, such as Lactobacillus and Akkermansia muciniphila. In conclusion, B. eggerthii S13-F8 demonstrates significant potential in mitigating severe diarrhea caused by 5-FU chemotherapy, providing a strong foundation for its development as a live biotherapeutic for CID treatment.
化疗引起的腹泻(CID)是癌症患者常见的胃肠道副作用,尤其与使用5-氟尿嘧啶(5-FU)有关。本研究旨在从健康个体的粪便中分离出多种拟杆菌菌株,并确定埃氏拟杆菌(B. eggerthii)S13-F8是缓解CID的最佳候选菌株。对埃氏拟杆菌S13-F8进行全基因组测序,以揭示其功能特征,并探索其对CID保护作用的潜在机制。使用包括腹泻严重程度、食物摄入量和体重变化在内的多个参数评估埃氏拟杆菌S13-F8的抗CID疗效。进行了包括血液检测、肠道组织病理学、结肠转录组学和粪便宏基因组学在内的综合分析,以阐明其潜在机制。在5-FU诱导的小鼠模型中,埃氏拟杆菌S13-F8显著减轻了体重减轻和腹泻。组织学检查显示,埃氏拟杆菌S13-F8保留了结肠组织中的绒毛高度与隐窝深度(V/C)比值,并保护了杯状细胞。基因表达分析表明,埃氏拟杆菌S13-F8上调了保护性标志物,如Aqp8、Slc26a3和粘蛋白相关基因(TFF3、FCGBP和Muc2),同时下调了促炎介质,包括IL-1α、IL-22和Cxcl2。此外,埃氏拟杆菌S13-F8通过抑制病原菌(铜绿假单胞菌、沙门氏菌、γ-变形菌和志贺氏菌)并富集有益菌群,如乳酸杆菌和嗜黏蛋白阿克曼氏菌,调节肠道微生物群组成。总之,埃氏拟杆菌S13-F8在减轻5-FU化疗引起的严重腹泻方面显示出巨大潜力,为其作为CID治疗的活生物治疗剂的开发提供了坚实基础。