Division of Gastroenterology, Hepatology, and Nutrition, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Nat Microbiol. 2020 Jun;5(6):838-847. doi: 10.1038/s41564-020-0694-0. Epub 2020 Apr 13.
Initial microbial colonization and later succession in the gut of human infants are linked to health and disease later in life. The timing of the appearance of the first gut microbiome, and the consequences for the early life metabolome, are just starting to be defined. Here, we evaluated the gut microbiome, proteome and metabolome in 88 African-American newborns using faecal samples collected in the first few days of life. Gut bacteria became detectable using molecular methods by 16 h after birth. Detailed analysis of the three most common species, Escherichia coli, Enterococcus faecalis and Bacteroides vulgatus, did not suggest a genomic signature for neonatal gut colonization. The appearance of bacteria was associated with reduced abundance of approximately 50 human proteins, decreased levels of free amino acids and an increase in products of bacterial fermentation, including acetate and succinate. Using flux balance modelling and in vitro experiments, we provide evidence that fermentation of amino acids provides a mechanism for the initial growth of E. coli, the most common early colonizer, under anaerobic conditions. These results provide a deep characterization of the first microbes in the human gut and show how the biochemical environment is altered by their appearance.
人类婴儿肠道内最初的微生物定植以及随后的演替与生命后期的健康和疾病有关。肠道微生物组首次出现的时间,以及对早期生命代谢组的影响,刚刚开始被定义。在这里,我们使用粪便样本评估了 88 名非裔美国新生儿的肠道微生物组、蛋白质组和代谢组,这些样本是在生命的头几天收集的。通过分子方法,在出生后 16 小时就可以检测到肠道细菌。对三种最常见的细菌,即大肠杆菌、粪肠球菌和普通拟杆菌的详细分析并未表明新生儿肠道定植具有基因组特征。细菌的出现与大约 50 个人类蛋白质丰度降低、游离氨基酸水平降低以及细菌发酵产物(包括乙酸盐和琥珀酸盐)增加有关。通过通量平衡建模和体外实验,我们提供了证据表明,在厌氧条件下,氨基酸发酵为最常见的早期定植细菌大肠杆菌的初始生长提供了一种机制。这些结果对人类肠道内的首批微生物进行了深入表征,并展示了其出现如何改变生化环境。
Nat Microbiol. 2020-4-13
Nat Rev Gastroenterol Hepatol. 2025-9-3
Cell Host Microbe. 2025-8-13
NPJ Vaccines. 2025-8-1
Microbiome Res Rep. 2024-11-9
Metabolomics. 2025-1-25
Microbiome. 2019-3-22
Proc Natl Acad Sci U S A. 2018-4-2
Nat Rev Gastroenterol Hepatol. 2018-1-24