Burz Sebastian D, Monnoye Magali, Philippe Catherine, Farin William, Ratziu Vlad, Strozzi Francesco, Paillarse Jean-Michel, Chêne Laurent, Blottière Hervé M, Gérard Philippe
Micalis Institute, Université Paris-Saclay, INRAE, AgroParisTech, 78350 Jouy-en-Josas, France.
Université Paris-Saclay, INRAE, MetaGenoPolis, 78350 Jouy-en-Josas, France.
Microorganisms. 2021 Jan 19;9(1):199. doi: 10.3390/microorganisms9010199.
Non-alcoholic fatty liver diseases (NAFLD) are associated with changes in the composition and metabolic activities of the gut microbiota. However, the causal role played by the gut microbiota in individual susceptibility to NAFLD and particularly at its early stage is still unclear. In this context, we transplanted the microbiota from a patient with fatty liver (NAFL) and from a healthy individual to two groups of mice. We first showed that the microbiota composition in recipient mice resembled the microbiota composition of their respective human donor. Following administration of a high-fructose, high-fat diet, mice that received the human NAFL microbiota (NAFLR) gained more weight and had a higher liver triglycerides level and higher plasma LDL cholesterol than mice that received the human healthy microbiota (HR). Metabolomic analyses revealed that it was associated with lower and higher plasma levels of glycine and 3-Indolepropionic acid in NAFLR mice, respectively. Moreover, several bacterial genera and OTUs were identified as differently represented in the NAFLR and HR microbiota and therefore potentially responsible for the different phenotypes observed. Altogether, our results confirm that the gut bacteria play a role in obesity and steatosis development and that targeting the gut microbiota may be a preventive or therapeutic strategy in NAFLD management.
非酒精性脂肪性肝病(NAFLD)与肠道微生物群的组成和代谢活动变化有关。然而,肠道微生物群在个体对NAFLD易感性中所起的因果作用,尤其是在疾病早期,仍不清楚。在此背景下,我们将来自一名脂肪肝患者(NAFL)和一名健康个体的微生物群移植到两组小鼠体内。我们首先表明,受体小鼠的微生物群组成与其各自人类供体的微生物群组成相似。在给予高果糖、高脂肪饮食后,接受人类NAFL微生物群的小鼠(NAFLR)比接受人类健康微生物群的小鼠(HR)体重增加更多,肝脏甘油三酯水平更高,血浆低密度脂蛋白胆固醇水平更高。代谢组学分析表明,这分别与NAFLR小鼠血浆中较低和较高水平的甘氨酸和3-吲哚丙酸有关。此外,还鉴定出几个细菌属和操作分类单元在NAFLR和HR微生物群中的表现不同,因此可能是观察到的不同表型的原因。总之,我们的结果证实肠道细菌在肥胖和脂肪变性发展中起作用,针对肠道微生物群可能是NAFLD管理中的一种预防或治疗策略。