Development of the Human Infant Intestinal Microbiota
Open accessAbstract
Almost immediately after a human being is born, so too is a new microbial ecosystem, one that resides in that person's gastrointestinal tract. Although it is a universal and integral part of human biology, the temporal progression of this process, the sources of the microbes that make up the ecosystem, how and why it varies from one infant to another, and how the composition of this ecosystem influences human physiology, development, and disease are still poorly understood. As a step toward systematically investigating these questions, we designed a microarray to detect and quantitate the small subunit ribosomal RNA (SSU rRNA) gene sequences of most currently recognized species and taxonomic groups of bacteria. We used this microarray, along with sequencing of cloned libraries of PCR-amplified SSU rDNA, to profile the microbial communities in an average of 26 stool samples each from 14 healthy, full-term human infants, including a pair of dizygotic twins, beginning with the first stool after birth and continuing at defined intervals throughout the first year of life. To investigate possible origins of the infant microbiota, we also profiled vaginal and milk samples from most of the mothers, and stool samples from all of the mothers, most of the fathers, and two siblings. The composition and temporal patterns of the microbial communities varied widely from baby to baby. Despite considerable temporal variation, the distinct features of each baby's microbial community were recognizable for intervals of weeks to months. The strikingly parallel temporal patterns of the twins suggested that incidental environmental exposures play a major role in determining the distinctive characteristics of the microbial community in each baby. By the end of the first year of life, the idiosyncratic microbial ecosystems in each baby, although still distinct, had converged toward a profile characteristic of the adult gastrointestinal tract.
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As the infant matures, strict anaerobes gradually take over as the dominant taxa, and overall diversity increases to adult-like levels by around 1-3 years of age, coinciding with weaning and a shift to solid food intake.
“As the infant matures, strict anaerobes gradually take over as the dominant taxa, and there is an increase in overall diversity to adult-like levels by around 1-3 years of age, coinciding with weaning and a shift to solid food intake (Koenig et al., 2011;Palmer et al., 2007;Yatsunenko et al., 2012).”
From The Microbiota-Gut-Brain Axis (2019) · cites this paper as Palmer et al., 2007
The Results (Overview of Microarray-Based Bacterial Population Profiles) say later colonizers tended to be strict anaerobes. The Results (Temporal Trends) report that stool communities at age 1 year and older resembled adult communities and that the transition often followed introduction of solid foods. They do not establish that overall diversity reached adult levels, or document a transition through age 3; the observed timing of shifts was not consistent. Page numbers are unavailable in our copy. (LLM, conf=0.88)
Experimental — accuracy not yet measuredIn the months to years after birth, gut microbial communities shift in response to life events such as solid food exposure, illnesses, and antibiotics, with gradual diversity increases and convergence to an adult-like microbiota.
“In the subsequent months to years, gut microbial communities continue to shift in response to key life events (e.g., exposure to solid foods, illnesses, antibiotics) with gradual increases in diversity and convergence to an “adult-like” microbiota9–11.”
From The gut Microbiome in adult and pediatric functional gastrointestinal disorders (2019) · cites this paper as [10]
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- Authors
- Palmer, C., Bik, E. M., DiGiulio, D. B., Relman, D. A., & Brown, P. O.
- Affiliations
- Stanford Medicine (US)
- VA Palo Alto Health Care System (US)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Brown, Patrick O
- Venue
- PLoS Biology
- Publisher
- Public Library of Science (PLoS)
- Published
- 2007-06-26
- Volume
- 5
- Issue
- 7
- Pages
- e177
- ISSN
- 1544-9173 (ISSN-L)
- 1545-7885
- PMC
- PMC1896187
- OpenAlex
- W2052969143
- Cited by
- 2,877
- References
- 62
- Citations by year
- 2026: 47 · 2025: 82 · 2024: 112 · 2023: 120 · 2022: 160 · 2021: 160 · 2020: 170 · 2019: 172 · 2018: 169 · 2017: 185 · 2016: 215 · 2015: 197 · 2014: 216 · 2013: 222 · 2012: 204
- FWCI
- 39.84
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- PLoS Biology (publishedVersion, public-domain)
- PubMed Central (publishedVersion, public-domain)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health (DP1OD000964)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Nursing › Nutrition and Dietetics › Infant Nutrition and Health
- Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
- Keywords
- infant gut microbiota, microbial community development, fecal samples, dizygotic twins, microbial origin, breast milk, environmental exposure, microbial diversity
- MeSH terms
- Adult, Age Factors, Bacteria, Base Sequence, Feces, Female, Humans, Infant, Infant, Newborn, Intestines, Male, Milk, Human, RNA, Bacterial, RNA, Ribosomal, Twins, Dizygotic, Vagina, Colony Count, Microbial, Ecosystem, DNA Primers, Oligonucleotide Array Sequence Analysis, Metagenome
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