Department of Agricultural Biotechnology, Center for Food and Bioconvergence, Research Institute for Agricultural and Life Sciences, Seoul National University, Seoul, Republic of Korea.
Institute for Liver and Digestive Diseases, Hallym University, Chuncheon, Republic of Korea.
Clin Transl Med. 2021 Dec;11(12):e634. doi: 10.1002/ctm2.634.
Although microbioa-based therapies have shown putative effects on the treatment of non-alcoholic fatty liver disease (NAFLD), it is not clear how microbiota-derived metabolites contribute to the prevention of NAFLD. We explored the metabolomic signature of Lactobacillus lactis and Pediococcus pentosaceus in NAFLD mice and its association in NAFLD patients.
We used Western diet-induced NAFLD mice, and L. lactis and P. pentosaceus were administered to animals in the drinking water at a concentration of 10 CFU/g for 8 weeks. NAFLD severity was determined based on liver/body weight, pathology and biochemistry markers. Caecal samples were collected for the metagenomics by 16S rRNA sequencing. Metabolite profiles were obtained from caecum, liver and serum. Human stool samples (healthy control [n = 22] and NAFLD patients [n = 23]) were collected to investigate clinical reproducibility for microbiota-derived metabolites signature and metabolomics biomarker.
L. lactis and P. pentosaceus supplementation effectively normalized weight ratio, NAFLD activity score, biochemical markers, cytokines and gut-tight junction. While faecal microbiota varied according to the different treatments, key metabolic features including short chain fatty acids (SCFAs), bile acids (BAs) and tryptophan metabolites were analogously restored by both probiotic supplementations. The protective effects of indole compounds were validated with in vitro and in vivo models, including anti-inflammatory effects. The metabolomic signatures were replicated in NAFLD patients, accompanied by the comparable levels of Firmicutes/Bacteroidetes ratio, which was significantly higher (4.3) compared with control (0.6). Besides, the consequent biomarker panel with six stool metabolites (indole, BAs, and SCFAs) showed 0.922 (area under the curve) in the diagnosis of NAFLD.
NAFLD progression was robustly associated with metabolic dys-regulations in the SCFAs, bile acid and indole compounds, and NAFLD can be accurately diagnosed using the metabolites. L. lactis and P. pentosaceus ameliorate NAFLD progression by modulating gut metagenomic and metabolic environment, particularly tryptophan pathway, of the gut-liver axis.
虽然基于微生物组的疗法已显示出对非酒精性脂肪性肝病(NAFLD)治疗的潜在作用,但微生物衍生代谢物如何有助于预防 NAFLD 尚不清楚。我们探索了乳酸乳球菌和戊糖片球菌在 NAFLD 小鼠中的代谢组学特征及其在 NAFLD 患者中的关联。
我们使用西方饮食诱导的 NAFLD 小鼠,将乳酸乳球菌和戊糖片球菌以 10 CFU/g 的浓度添加到饮用水中,连续 8 周对动物进行处理。根据肝/体重比、病理和生化标志物来确定 NAFLD 的严重程度。收集盲肠样本进行 16S rRNA 测序的宏基因组学分析。获得盲肠、肝脏和血清中的代谢物图谱。收集人类粪便样本(健康对照组[n=22]和 NAFLD 患者[n=23]),以研究微生物衍生代谢物特征和代谢组学生物标志物的临床重现性。
乳酸乳球菌和戊糖片球菌的补充有效地使体重比、NAFLD 活性评分、生化标志物、细胞因子和肠道紧密连接正常化。虽然粪便微生物组因不同的处理而有所不同,但关键的代谢特征,包括短链脂肪酸(SCFAs)、胆汁酸(BAs)和色氨酸代谢物,都被两种益生菌补充剂类似地恢复。吲哚化合物的保护作用通过体外和体内模型得到了验证,包括抗炎作用。代谢组学特征在 NAFLD 患者中得到了复制,同时伴随着类似的厚壁菌门/拟杆菌门比值,与对照组(0.6)相比,该比值显著更高(4.3)。此外,由六种粪便代谢物(吲哚、BAs 和 SCFAs)组成的后续生物标志物谱在诊断 NAFLD 时具有 0.922 的曲线下面积(AUC)。
NAFLD 的进展与 SCFAs、胆汁酸和吲哚化合物的代谢失调密切相关,NAFLD 可以使用这些代谢物进行准确诊断。乳酸乳球菌和戊糖片球菌通过调节肠道-肝脏轴的肠道宏基因组和代谢环境,特别是色氨酸途径,改善 NAFLD 的进展。