Department of Bioinformatics and Genomics, University of North Carolina, Charlotte, North Carolina 28223, USA.
Gastroenterology. 2011 Mar;140(3):976-86. doi: 10.1053/j.gastro.2010.11.049. Epub 2010 Dec 1.
BACKGROUND & AIMS: Nonalcoholic fatty liver disease affects up to 30% of the US population, but the mechanisms underlying this condition are incompletely understood. We investigated how diet standardization and choline deficiency influence the composition of the microbial community in the human gastrointestinal tract and the development of fatty liver under conditions of choline deficiency.
We performed a 2-month inpatient study of 15 female subjects who were placed on well-controlled diets in which choline levels were manipulated. We used 454-FLX pyrosequencing of 16S ribosomal RNA bacterial genes to characterize microbiota in stool samples collected over the course of the study.
The compositions of the gastrointestinal microbial communities changed with choline levels of diets; each individual's microbiome remained distinct for the duration of the experiment, even though all subjects were fed identical diets. Variations between subjects in levels of Gammaproteobacteria and Erysipelotrichi were directly associated with changes in liver fat in each subject during choline depletion. Levels of these bacteria, change in amount of liver fat, and a single nucleotide polymorphism that affects choline were combined into a model that accurately predicted the degree to which subjects developed fatty liver on a choline-deficient diet.
Host factors and gastrointestinal bacteria each respond to dietary choline deficiency, although the gut microbiota remains distinct in each individual. We identified bacterial biomarkers of fatty liver that result from choline deficiency, adding to the accumulating evidence that gastrointestinal microbes have a role in metabolic disorders.
非酒精性脂肪性肝病影响了多达 30%的美国人口,但该疾病的发病机制尚不完全清楚。我们研究了饮食标准化和胆碱缺乏如何影响人类胃肠道微生物群落的组成,并在胆碱缺乏的情况下影响脂肪肝的发生。
我们对 15 名女性进行了为期 2 个月的住院研究,这些女性的饮食受到严格控制,胆碱水平可以进行人为操纵。我们使用 454-FLX 焦磷酸测序对 16S 核糖体 RNA 细菌基因进行测序,以分析研究过程中采集的粪便样本中的微生物群。
胃肠道微生物群落的组成随饮食中的胆碱水平而变化;尽管所有受试者都接受相同的饮食,但每个人的微生物组在整个实验过程中仍然保持独特。在胆碱耗竭期间,个体间的γ变形菌门和丹毒丝菌科的水平变化与每个受试者肝脏脂肪的变化直接相关。这些细菌的水平、肝脏脂肪量的变化以及影响胆碱的单核苷酸多态性被组合成一个模型,该模型可以准确预测受试者在胆碱缺乏饮食中发生脂肪肝的程度。
尽管肠道微生物群在每个个体中仍然保持独特,但宿主因素和胃肠道细菌都对饮食中的胆碱缺乏做出了反应。我们确定了由胆碱缺乏引起的脂肪肝的细菌生物标志物,这增加了越来越多的证据表明胃肠道微生物在代谢紊乱中起作用。