Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Center for Gut Microbiome and Nutrition Research, Washington University School of Medicine, St. Louis, MO 63110, USA.
Science. 2019 Jul 12;365(6449). doi: 10.1126/science.aau4732.
To examine the contributions of impaired gut microbial community development to childhood undernutrition, we combined metabolomic and proteomic analyses of plasma samples with metagenomic analyses of fecal samples to characterize the biological state of Bangladeshi children with severe acute malnutrition (SAM) as they transitioned, after standard treatment, to moderate acute malnutrition (MAM) with persistent microbiota immaturity. Host and microbial effects of microbiota-directed complementary food (MDCF) prototypes targeting weaning-phase bacterial taxa underrepresented in SAM and MAM microbiota were characterized in gnotobiotic mice and gnotobiotic piglets colonized with age- and growth-discriminatory bacteria. A randomized, double-blind controlled feeding study identified a lead MDCF that changes the abundances of targeted bacteria and increases plasma biomarkers and mediators of growth, bone formation, neurodevelopment, and immune function in children with MAM.
为了探究受损肠道微生物群落发育对儿童营养不良的影响,我们结合了血浆样本的代谢组学和蛋白质组学分析以及粪便样本的宏基因组学分析,以描述孟加拉国严重急性营养不良(SAM)儿童在接受标准治疗后向中度急性营养不良(MAM)过渡时的生物学状态,此时他们的肠道微生物群仍不成熟。针对 SAM 和 MAM 微生物群中代表性不足的断奶期细菌类群,我们通过靶向微生物定向补充食品(MDCF)原型对共生小鼠和定植了具有年龄和生长区分能力的细菌的共生仔猪进行了宿主和微生物效应研究。一项随机、双盲对照喂养研究确定了一种 MDCF 的先导配方,它改变了目标细菌的丰度,并增加了患有 MAM 的儿童的血浆生物标志物和生长、骨形成、神经发育和免疫功能的调节剂。