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Deterministic transition of enterotypes shapes the infant gut microbiome at an early age

BACKGROUND: The succession of the gut microbiota during the first few years plays a vital role in human development. We elucidate the characteristics and alternations of the infant gut microbiota to better understand the correlation between infant health and microbiota maturation. RESULTS: We collec...

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Autores principales: Xiao, Liwen, Wang, Jinfeng, Zheng, Jiayong, Li, Xiaoqing, Zhao, Fangqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383385/
https://www.ncbi.nlm.nih.gov/pubmed/34429130
http://dx.doi.org/10.1186/s13059-021-02463-3
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author Xiao, Liwen
Wang, Jinfeng
Zheng, Jiayong
Li, Xiaoqing
Zhao, Fangqing
author_facet Xiao, Liwen
Wang, Jinfeng
Zheng, Jiayong
Li, Xiaoqing
Zhao, Fangqing
author_sort Xiao, Liwen
collection PubMed
description BACKGROUND: The succession of the gut microbiota during the first few years plays a vital role in human development. We elucidate the characteristics and alternations of the infant gut microbiota to better understand the correlation between infant health and microbiota maturation. RESULTS: We collect 13,776 fecal samples or datasets from 1956 infants between 1 and 3 years of age, based on multi-population cohorts covering 17 countries. The characteristics of the gut microbiota are analyzed based on enterotype and an ecological model. Clinical information (n = 2287) is integrated to understand outcomes of different developmental patterns. Infants whose gut microbiota are dominated by Firmicutes and Bifidobacterium exhibit typical characteristics of early developmental stages, such as unstable community structure and low microbiome maturation, while those driven by Bacteroides and Prevotella are characterized by higher diversity and stronger connections in the gut microbial community. We further reveal a geography-related pattern in global populations. Through ecological modeling and functional analysis, we demonstrate that the transition of the gut microbiota from infants towards adults follows a deterministic pattern; as infants grow up, the dominance of Firmicutes and Bifidobacterium is replaced by that of Bacteroides and Prevotella, along with shifts in specific metabolic pathways. CONCLUSIONS: By leveraging the extremely large datasets and enterotype-based microbiome analysis, we decipher the colonization and transition of the gut microbiota in infants from a new perspective. We further introduce an ecological model to estimate the tendency of enterotype transitions, and demonstrated that the transition of infant gut microbiota was deterministic and predictable. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02463-3.
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spelling pubmed-83833852021-08-25 Deterministic transition of enterotypes shapes the infant gut microbiome at an early age Xiao, Liwen Wang, Jinfeng Zheng, Jiayong Li, Xiaoqing Zhao, Fangqing Genome Biol Research BACKGROUND: The succession of the gut microbiota during the first few years plays a vital role in human development. We elucidate the characteristics and alternations of the infant gut microbiota to better understand the correlation between infant health and microbiota maturation. RESULTS: We collect 13,776 fecal samples or datasets from 1956 infants between 1 and 3 years of age, based on multi-population cohorts covering 17 countries. The characteristics of the gut microbiota are analyzed based on enterotype and an ecological model. Clinical information (n = 2287) is integrated to understand outcomes of different developmental patterns. Infants whose gut microbiota are dominated by Firmicutes and Bifidobacterium exhibit typical characteristics of early developmental stages, such as unstable community structure and low microbiome maturation, while those driven by Bacteroides and Prevotella are characterized by higher diversity and stronger connections in the gut microbial community. We further reveal a geography-related pattern in global populations. Through ecological modeling and functional analysis, we demonstrate that the transition of the gut microbiota from infants towards adults follows a deterministic pattern; as infants grow up, the dominance of Firmicutes and Bifidobacterium is replaced by that of Bacteroides and Prevotella, along with shifts in specific metabolic pathways. CONCLUSIONS: By leveraging the extremely large datasets and enterotype-based microbiome analysis, we decipher the colonization and transition of the gut microbiota in infants from a new perspective. We further introduce an ecological model to estimate the tendency of enterotype transitions, and demonstrated that the transition of infant gut microbiota was deterministic and predictable. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02463-3. BioMed Central 2021-08-24 /pmc/articles/PMC8383385/ /pubmed/34429130 http://dx.doi.org/10.1186/s13059-021-02463-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Xiao, Liwen
Wang, Jinfeng
Zheng, Jiayong
Li, Xiaoqing
Zhao, Fangqing
Deterministic transition of enterotypes shapes the infant gut microbiome at an early age
title Deterministic transition of enterotypes shapes the infant gut microbiome at an early age
title_full Deterministic transition of enterotypes shapes the infant gut microbiome at an early age
title_fullStr Deterministic transition of enterotypes shapes the infant gut microbiome at an early age
title_full_unstemmed Deterministic transition of enterotypes shapes the infant gut microbiome at an early age
title_short Deterministic transition of enterotypes shapes the infant gut microbiome at an early age
title_sort deterministic transition of enterotypes shapes the infant gut microbiome at an early age
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383385/
https://www.ncbi.nlm.nih.gov/pubmed/34429130
http://dx.doi.org/10.1186/s13059-021-02463-3
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