Cargando…

Evolution of the Gut Microbiome in Early Childhood: A Cross-Sectional Study of Chinese Children

Temporal development of the human gut microbiome from infancy to childhood is driven by a variety of factors. We surveyed the fecal microbiome of 729 Chinese children aged 0–36 months, aiming to identify the age-specific patterns of microbiota succession, and evaluate the impact of birth mode, gende...

Descripción completa

Detalles Bibliográficos
Autores principales: Niu, Jing, Xu, Long, Qian, Yun, Sun, Zhuo, Yu, Dongbao, Huang, Jiandong, Zhou, Xiaolin, Wang, Yizhong, Zhang, Ting, Ren, Rongrong, Li, Zhengpeng, Yu, Jialin, Gao, Xuefeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7169428/
https://www.ncbi.nlm.nih.gov/pubmed/32346375
http://dx.doi.org/10.3389/fmicb.2020.00439
_version_ 1783523787540529152
author Niu, Jing
Xu, Long
Qian, Yun
Sun, Zhuo
Yu, Dongbao
Huang, Jiandong
Zhou, Xiaolin
Wang, Yizhong
Zhang, Ting
Ren, Rongrong
Li, Zhengpeng
Yu, Jialin
Gao, Xuefeng
author_facet Niu, Jing
Xu, Long
Qian, Yun
Sun, Zhuo
Yu, Dongbao
Huang, Jiandong
Zhou, Xiaolin
Wang, Yizhong
Zhang, Ting
Ren, Rongrong
Li, Zhengpeng
Yu, Jialin
Gao, Xuefeng
author_sort Niu, Jing
collection PubMed
description Temporal development of the human gut microbiome from infancy to childhood is driven by a variety of factors. We surveyed the fecal microbiome of 729 Chinese children aged 0–36 months, aiming to identify the age-specific patterns of microbiota succession, and evaluate the impact of birth mode, gender, geographical location, and gastrointestinal tract symptoms on the shaping of the gut microbiome. We demonstrated that phylogenetic diversity of the gut microbiome increased gradually over time, which was accompanied by an increase in Bacteroidetes and a reduction in Proteobacteria species. Analysis of community-wide phenotypes revealed a succession from aerobic bacteria and anaerobic bacteria to facultative anaerobes, and from Gram-negative to Gram-positive species during gut microbiota development in early childhood. The metabolic functions of the gut microbiome shifted tremendously alongside early physiological development, including an increase in alanine, aspartate, and glutamate metabolism, and a reduction in glutathione, fatty acid, and tyrosine metabolism. During the first year of life, the Bacteroidetes phylum was less abundant in children born by casarean section compared with those delivered vaginally. The Enterococcaceae family, a group of facultative anaerobic microorganisms with pathogenic potential, was predominant in preterm infants. No measurable effect of maternal antibiotic exposure on gut microbiota development was found in the first 3 years of life. The relative abundances of Coriobacteriaceae and Streptococcaceae families, and Megasphaera genus were found to be higher in girls than in boys. Among the three first-tier Chinese cities, children born and fed in Beijing had a higher abundance of Enterococcaceae and Lachnospiraceae families, and Shenzhen children had a higher abundance of Fusobacteriaceae. The families Alcaligenaceae, Bacteroidaceae, and Porphyromonadaceae were more abundant in children with constipation, whereas the relative abundance of the Clostridium genus was higher in those with diarrhea.
format Online
Article
Text
id pubmed-7169428
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-71694282020-04-28 Evolution of the Gut Microbiome in Early Childhood: A Cross-Sectional Study of Chinese Children Niu, Jing Xu, Long Qian, Yun Sun, Zhuo Yu, Dongbao Huang, Jiandong Zhou, Xiaolin Wang, Yizhong Zhang, Ting Ren, Rongrong Li, Zhengpeng Yu, Jialin Gao, Xuefeng Front Microbiol Microbiology Temporal development of the human gut microbiome from infancy to childhood is driven by a variety of factors. We surveyed the fecal microbiome of 729 Chinese children aged 0–36 months, aiming to identify the age-specific patterns of microbiota succession, and evaluate the impact of birth mode, gender, geographical location, and gastrointestinal tract symptoms on the shaping of the gut microbiome. We demonstrated that phylogenetic diversity of the gut microbiome increased gradually over time, which was accompanied by an increase in Bacteroidetes and a reduction in Proteobacteria species. Analysis of community-wide phenotypes revealed a succession from aerobic bacteria and anaerobic bacteria to facultative anaerobes, and from Gram-negative to Gram-positive species during gut microbiota development in early childhood. The metabolic functions of the gut microbiome shifted tremendously alongside early physiological development, including an increase in alanine, aspartate, and glutamate metabolism, and a reduction in glutathione, fatty acid, and tyrosine metabolism. During the first year of life, the Bacteroidetes phylum was less abundant in children born by casarean section compared with those delivered vaginally. The Enterococcaceae family, a group of facultative anaerobic microorganisms with pathogenic potential, was predominant in preterm infants. No measurable effect of maternal antibiotic exposure on gut microbiota development was found in the first 3 years of life. The relative abundances of Coriobacteriaceae and Streptococcaceae families, and Megasphaera genus were found to be higher in girls than in boys. Among the three first-tier Chinese cities, children born and fed in Beijing had a higher abundance of Enterococcaceae and Lachnospiraceae families, and Shenzhen children had a higher abundance of Fusobacteriaceae. The families Alcaligenaceae, Bacteroidaceae, and Porphyromonadaceae were more abundant in children with constipation, whereas the relative abundance of the Clostridium genus was higher in those with diarrhea. Frontiers Media S.A. 2020-04-03 /pmc/articles/PMC7169428/ /pubmed/32346375 http://dx.doi.org/10.3389/fmicb.2020.00439 Text en Copyright © 2020 Niu, Xu, Qian, Sun, Yu, Huang, Zhou, Wang, Zhang, Ren, Li, Yu and Gao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Niu, Jing
Xu, Long
Qian, Yun
Sun, Zhuo
Yu, Dongbao
Huang, Jiandong
Zhou, Xiaolin
Wang, Yizhong
Zhang, Ting
Ren, Rongrong
Li, Zhengpeng
Yu, Jialin
Gao, Xuefeng
Evolution of the Gut Microbiome in Early Childhood: A Cross-Sectional Study of Chinese Children
title Evolution of the Gut Microbiome in Early Childhood: A Cross-Sectional Study of Chinese Children
title_full Evolution of the Gut Microbiome in Early Childhood: A Cross-Sectional Study of Chinese Children
title_fullStr Evolution of the Gut Microbiome in Early Childhood: A Cross-Sectional Study of Chinese Children
title_full_unstemmed Evolution of the Gut Microbiome in Early Childhood: A Cross-Sectional Study of Chinese Children
title_short Evolution of the Gut Microbiome in Early Childhood: A Cross-Sectional Study of Chinese Children
title_sort evolution of the gut microbiome in early childhood: a cross-sectional study of chinese children
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7169428/
https://www.ncbi.nlm.nih.gov/pubmed/32346375
http://dx.doi.org/10.3389/fmicb.2020.00439
work_keys_str_mv AT niujing evolutionofthegutmicrobiomeinearlychildhoodacrosssectionalstudyofchinesechildren
AT xulong evolutionofthegutmicrobiomeinearlychildhoodacrosssectionalstudyofchinesechildren
AT qianyun evolutionofthegutmicrobiomeinearlychildhoodacrosssectionalstudyofchinesechildren
AT sunzhuo evolutionofthegutmicrobiomeinearlychildhoodacrosssectionalstudyofchinesechildren
AT yudongbao evolutionofthegutmicrobiomeinearlychildhoodacrosssectionalstudyofchinesechildren
AT huangjiandong evolutionofthegutmicrobiomeinearlychildhoodacrosssectionalstudyofchinesechildren
AT zhouxiaolin evolutionofthegutmicrobiomeinearlychildhoodacrosssectionalstudyofchinesechildren
AT wangyizhong evolutionofthegutmicrobiomeinearlychildhoodacrosssectionalstudyofchinesechildren
AT zhangting evolutionofthegutmicrobiomeinearlychildhoodacrosssectionalstudyofchinesechildren
AT renrongrong evolutionofthegutmicrobiomeinearlychildhoodacrosssectionalstudyofchinesechildren
AT lizhengpeng evolutionofthegutmicrobiomeinearlychildhoodacrosssectionalstudyofchinesechildren
AT yujialin evolutionofthegutmicrobiomeinearlychildhoodacrosssectionalstudyofchinesechildren
AT gaoxuefeng evolutionofthegutmicrobiomeinearlychildhoodacrosssectionalstudyofchinesechildren