Lu Haifeng, Chen Liang, Pan Xiaxia, Yao Yujun, Zhang Hua, Zhu Xiaofei, Lou Xiaobin, Zhu Chunxia, Wang Jun, Li Lanjuan, Wu Zhongwen
State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
National Clinical Research Center for Infectious Diseases, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Front Med (Lausanne). 2021 Oct 14;8:762930. doi: 10.3389/fmed.2021.762930. eCollection 2021.
Cirrhosis is a common chronic liver disease characterized by irreversible diffuse liver damage. Intestinal microbiome dysbiosis and metabolite dysfunction contribute to the development of cirrhosis. Lactitol (4-β-D-galactopyranosyl-D-glucitol) was previously reported to promote the growth of intestinal . However, the effect of lactitol on the intestinal microbiome and fecal short-chain fatty acids (SCFAs) and bile acids (BAs) and the interactions among these factors in cirrhotic patients pre- and post-lactitol treatment remain poorly understood. Here, using shotgun metagenomics and targeted metabolomics methods. we found that health-promoting lactic acid bacteria, including , and , were increased after lactitol intervention, and significant decrease of pathogen and associated antibiotic resistant genes /virulence factors. Functionally, pathways including Pseudomonas aeruginosa biofilm formation, endotoxin biosynthesis, and horizontal transfer of pathogenic genes were decreased in cirrhotic patients after 4-week lactitol intervention compared with before treatment. We identified lactitol-associated metagenomic changes, and provide insight into the understanding of the roles of lactitol in modulating gut microbiome in cirrhotic patients.
肝硬化是一种常见的慢性肝病,其特征是肝脏出现不可逆的弥漫性损伤。肠道微生物群失调和代谢物功能障碍会促使肝硬化的发展。乳糖醇(4-β-D-吡喃半乳糖基-D-葡萄糖醇)此前被报道可促进肠道生长。然而,乳糖醇对肝硬化患者肠道微生物群、粪便短链脂肪酸(SCFAs)和胆汁酸(BAs)的影响以及这些因素之间在乳糖醇治疗前后的相互作用仍知之甚少。在此,我们使用鸟枪法宏基因组学和靶向代谢组学方法,发现包括[具体乳酸菌名称未给出]等在内的有益健康的乳酸菌在乳糖醇干预后增加,病原体[具体病原体名称未给出]及相关抗生素抗性基因/毒力因子显著减少。在功能方面,与治疗前相比,肝硬化患者在接受4周乳糖醇干预后,包括铜绿假单胞菌生物膜形成、内毒素生物合成和致病基因水平转移等途径减少。我们确定了与乳糖醇相关的宏基因组变化,并为理解乳糖醇在调节肝硬化患者肠道微生物群中的作用提供了见解。