TY - JOUR
T1 - Bacterial colonization reprograms the neonatal gut metabolome
AU - Bittinger, Kyle
AU - Zhao, Chunyu
AU - Li, Yun
AU - Ford, Eileen
AU - Friedman, Elliot S.
AU - Ni, Josephine
AU - Kulkarni, Chiraag V.
AU - Cai, Jingwei
AU - Tian, Yuan
AU - Liu, Qing
AU - Patterson, Andrew D.
AU - Sarkar, Debolina
AU - Chan, Siu H.J.
AU - Maranas, Costas
AU - Saha-Shah, Anumita
AU - Lund, Peder
AU - Garcia, Benjamin A.
AU - Mattei, Lisa M.
AU - Gerber, Jeffrey S.
AU - Elovitz, Michal A.
AU - Kelly, Andrea
AU - DeRusso, Patricia
AU - Kim, Dorothy
AU - Hofstaedter, Casey E.
AU - Goulian, Mark
AU - Li, Hongzhe
AU - Bushman, Frederic D.
AU - Zemel, Babette S.
AU - Wu, Gary D.
N1 - Funding Information:
Partial funding was provided by an unrestricted donation from the American Beverage Foundation for a Healthy America to the Children’s Hospital of Philadelphia to support the Healthy Weight Program. This study was also supported by the Research Institute of the Children’s Hospital of Philadelphia, The PennCHOP Microbiome Program, the Pennsylvania State University Department of Chemical Engineering, the USDA National Institute of Food and Agriculture (project no. PEN04607, accession no. 1009993; to A.D.P.), the Pennsylvania Department of Health using Tobacco C.U.R.E. Funds (to A.D.P.), the NIH National Center for Research Resources Clinical and Translational Science Program (grant no. UL1TR001878), the National Institute of Digestive Diseases and Disorders of the Kidney (grant no. R01DK107565), a Tobacco Formula grant under the Commonwealth Universal Research Enhancement program (grant no. SAP 4100068710), Research Electronic Data Capture (REDCap), the Human-Microbial Analytic and Repository Core of the Center for Molecular Studies in Digestive and Liver Disease (grant no. P30 DK050306), the Research Scholar Award from the American Gastroenterological Association, the Howard Hughes Medical Institute Medical Fellowship, NIH 2T32CA009140 and Crohn’s and Colitis Foundation, and the Center for Bioenergy Innovation (grant no. DE-AC05-00OR22725). Special thanks go to the mothers and their infants who participated in this research study.
Publisher Copyright:
© 2020, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2020/6/1
Y1 - 2020/6/1
N2 - 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.
AB - 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.
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U2 - 10.1038/s41564-020-0694-0
DO - 10.1038/s41564-020-0694-0
M3 - Article
C2 - 32284564
AN - SCOPUS:85083343253
SN - 2058-5276
VL - 5
SP - 838
EP - 847
JO - Nature Microbiology
JF - Nature Microbiology
IS - 6
ER -