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肠道微生物组的发育与儿童营养不良。

Gut microbiome development and childhood undernutrition.

机构信息

The Edison Family Center for Genome Sciences and Systems Biology, Washington University in St. Louis, St. Louis, MO 63110, USA; Center for Gut Microbiome Research, Washington University in St. Louis, St. Louis, MO 63110, USA.

International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka 1212, Bangladesh.

出版信息

Cell Host Microbe. 2022 May 11;30(5):617-626. doi: 10.1016/j.chom.2022.04.002.

Abstract

Forty-five percent of deaths among children under 5 years of age are associated with undernutrition. Globally, almost 200 million children exhibit the two major forms of undernutrition-wasting (low weight-for-height) or stunting (low height-for-age), with many affected by both. Undernutrition is not due to food insecurity alone. Growing evidence indicates that perturbed postnatal gut microbiome development contributes to its pathogenesis. This perspective focuses on defining and repairing these defects in gut microbiome development. We describe an approach that involves the analysis of well-phenotyped human cohorts, followed by preclinical studies using gnotobiotic animals colonized with microbiota from these cohorts. Additionally, these models can be used to identify therapeutic targets and candidates that can then be tested clinically. Furthermore, introducing pretreatment microbiota from trial participants into gnotobiotic animals and re-enacting trial conditions allow mechanisms to be dissected. We highlight these recent advances as well as gaps in existing knowledge that present opportunities for future research.

摘要

5 岁以下儿童死亡的 45%与营养不良有关。在全球范围内,几乎有 2 亿儿童表现出两种主要形式的营养不良——消瘦(身高体重低)或发育迟缓(身高年龄低),许多儿童同时受到两种影响。营养不良不仅仅是由于粮食不安全造成的。越来越多的证据表明,肠道微生物组发育的紊乱与营养不良的发病机制有关。本观点重点在于定义和修复肠道微生物组发育的这些缺陷。我们描述了一种方法,涉及对表型良好的人类队列进行分析,然后使用来自这些队列的微生物群定植的无菌动物进行临床前研究。此外,这些模型可用于确定可在临床上进行测试的治疗靶点和候选物。此外,将来自试验参与者的预处理微生物群引入无菌动物,并重新模拟试验条件,使我们能够剖析其中的机制。我们强调了这些最近的进展,以及现有知识中的空白,这些空白为未来的研究提供了机会。

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