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Altered gut microbial energy and metabolism in children with non-alcoholic fatty liver disease

机译:非酒精性脂肪肝患儿肠道微生物能量和代谢改变

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摘要

Obesity is becoming the new pediatric epidemic. Non-alcoholic fatty liver disease (NAFLD) is frequently associated with obesity and has become the most common cause of pediatric liver disease. The gut microbiome is the major metabolic organ and determines how calories are processed, serving as a caloric gate and contributing towards the pathogenesis of NAFLD. The goal of this study is to examine gut microbial profiles in children with NAFLD using phylogenetic, metabolomic, metagenomic and proteomic approaches. Fecal samples were obtained from obese children with or without NAFLD and healthy lean children. Stool specimens were subjected to 16S rRNA gene microarray, shotgun sequencing, mass spectroscopy for proteomics and NMR spectroscopy for metabolite analysis. Children with NAFLD had more abundant Gammaproteobacteria and Prevotella and significantly higher levels of ethanol, with differential effects on short chain fatty acids. This group also had increased genomic and protein abundance for energy production with a reduction in carbohydrate and amino acid metabolism and urea cycle and urea transport systems. The metaproteome and metagenome showed similar findings. The gut microbiome in pediatric NAFLD is distinct from lean healthy children with more alcohol production and pathways allocated to energy metabolism over carbohydrate and amino acid metabolism, which would contribute to development of disease.
机译:肥胖正在成为新的小儿流行病。非酒精性脂肪肝疾病(NAFLD)通常与肥胖症相关,并且已成为小儿肝病的最常见原因。肠道微生物组是主要的代谢器官,它决定卡路里的处理方式,充当热量的门并促进NAFLD的发病。这项研究的目的是使用系统发育,代谢组学,宏基因组学和蛋白质组学方法检查NAFLD儿童的肠道微生物谱。从有或没有NAFLD的肥胖儿童和健康的瘦儿童中获得粪便样品。粪便标本经过16S rRNA基因微阵列处理,shot弹枪测序,蛋白质组学质谱分析和代谢物分析NMR谱分析。患有NAFLD的儿童具有更丰富的γ-变形杆菌和Prevotella,乙醇含量明显更高,对短链脂肪酸的影响不同。该组还增加了用于能量产生的基因组和蛋白质丰度,同时减少了碳水化合物和氨基酸代谢以及尿素循环和尿素转运系统。元蛋白质组和元基因组显示相似的发现。小儿NAFLD的肠道微生物组与瘦弱的健康儿童截然不同,他们的酒精产量更高,并且分配给能量代谢的途径超过碳水化合物和氨基酸代谢,这将有助于疾病的发展。

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