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Updated: Jun 2, 2025

Applying Advanced In Vitro Culturing Technology to Study the Human Gut Microbiota
Published on: February 15, 2019
Early life microbial succession in the gut follows common patterns in humans across the globe
Guilherme Fahur Bottino1, Kevin S Bonham1, Fadheela Patel2
1Department of Biological Sciences, Wellesley College, Wellesley, MA, USA.
Insights
Scientists developed a model to estimate infant age using gut microbiome data, revealing universal developmental patterns. This "microbiome age" tool aids in assessing early gut maturation and child development.
Area of Science:
- Microbiology
- Developmental Biology
- Bioinformatics
Background:
- Understanding infant gut microbiome dynamics is vital for child health.
- No existing normative model accurately tracks early gut microbial development.
Purpose of the Study:
- To develop a normative model for infant gut microbiome maturation.
- To estimate infant age using microbial taxonomic data with high temporal resolution.
Main Methods:
- Trained a random forest model on 3154 metagenomic samples from 1827 infants globally.
- Utilized gut microbial taxonomic relative abundances to predict child age.
- Analyzed key taxonomic predictors and functional gene trends.
Main Results:
- Achieved a root mean square error of 2.56 months in age estimation.
- Identified key microbial shifts, including decreasing Bifidobacterium spp. and increasing Faecalibacterium prausnitzii.
- Demonstrated conserved microbial succession patterns across diverse populations, indicating universal developmental trajectories.
Conclusions:
- The developed model provides a reliable
- microbiome age
- benchmark for assessing early gut maturation.
- Microbial succession in the infant gut follows conserved, universal developmental pathways.
- This tool can complement existing measures of child development.
Abstract:
Characterizing the dynamics of microbial community succession in the infant gut microbiome is crucial for understanding child health and development, but no normative model currently exists. Here, we estimate child age using gut microbial taxonomic relative abundances from metagenomes, with high temporal resolution (±3 months) for the first 1.5 years of life. Using 3154 samples from 1827 infants across 12 countries, we trained a random forest model, achieving a root mean square error of 2.56 months. We identified key taxonomic predictors of age, including declines in Bifidobacterium spp. and increases in Faecalibacterium prausnitzii and Lachnospiraceae. Microbial succession patterns are conserved across infants from diverse human populations, suggesting universal developmental trajectories. Functional analysis confirmed trends in key microbial genes involved in feeding transitions and dietary exposures. This model provides a normative benchmark of "microbiome age" for assessing early gut maturation that may be used alongside other measures of child development.
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