# The triad of maternal gut-breast milk-infant gut microbial transmission in early life as a critical pathway for microbial inheritance

**Authors:** Yanli Du, Jing Cheng, Ruixia Xie, Yongke Zhang, Zhili Huang, Gang Jin, Xiulan Dong, Dayong Sun, Bingxiang Yang, Zongli Han, Xiangyu Wang

PMC · DOI: 10.1080/19490976.2025.2574928 · 2025-11-16

## TL;DR

This study explores how microbes from a mother's gut are passed to her infant through breast milk, shaping the infant's gut microbiota from birth.

## Contribution

The study reveals the maternal gut-breast milk-infant gut pathway as a key route for microbial inheritance in early life.

## Key findings

- Exclusively breastfed newborns' gut microbiota on day one primarily comes from breast milk.
- Bifidobacteria is a notable example of microbes transferred via the maternal gut-breast milk-infant gut pathway.
- Microbial diversity in breastfed infants is remarkably high from the first day of life.

## Abstract

Although maternal microbial inheritance is recognized, the temporal dynamics of how the maternal gut microbiota shapes the infant gut microbiota via specific routes remain unexplored. We performed longitudinal, multi-site microbiota sampling in 30 mother-infant pairs (including 14 exclusive breastfeeding and 16 mixed breastfeeding) from birth to one month, stratified by lactation stages. To trace the origin of breast milk microbiota, we also analyzed colostrum and gut samples from 8 postpartum mothers separated from their infants. Using 16S RNA sequencing, we analyzed microbial diversity and correlations across lactation stages. The results demonstrated that the gut microbiota of exclusively breastfed newborns on the first day primarily originated from breast milk and exhibited remarkably high diversity. We identified maternal gut-breast milk-infant gut transfer as a key pathway for microbial inheritance, with Bifidobacteria being a compelling example. These findings provide evidence for this route as a mechanism for inherited microbial diversity.

## Full-text entities

- **Genes:** PCOS1 (polycystic ovary syndrome 1) [NCBI Gene 5120] {aka PCO, PCO1}
- **Diseases:** hypertension (MESH:D006973), obesity (MESH:D009765), infection (MESH:D007239), otitis media (MESH:D010033), leukemia (MESH:D007938), type 2 diabetes (MESH:D003924), communicable (MESH:D003141), food allergy (MESH:D005512), gestational diabetes (MESH:D016640), MNS (MESH:D001010), atopic dermatitis (MESH:D003876), EB (MESH:C565501), sudden infant death syndrome (MESH:D013398), pneumonia (MESH:D011014), diarrhea (MESH:D003967), breast and ovarian cancer (MESH:D061325)
- **Chemicals:** agarose (MESH:D012685), glucose (MESH:D005947), nitrogen (MESH:D009584), butyrate (MESH:D002087), fatty acid (MESH:D005227), lactate (MESH:D019344), oligosaccharides (MESH:D009844), polyphenols (MESH:D059808), HMOs (-), oxygen (MESH:D010100), prebiotic (MESH:D056692), acetate (MESH:D000085), water (MESH:D014867)
- **Species:** Shigella (genus) [taxon 620], Enterobacteriaceae (enterobacteria, family) [taxon 543], Veillonella (genus) [taxon 29465], Enterobacter (genus) [taxon 547], Faecalibacterium (genus) [taxon 216851], Prevotella (genus) [taxon 838], Klebsiella (genus) [taxon 570], Clostridium (genus) [taxon 1485], Streptococcus (genus) [taxon 1301], Escherichia coli (E. coli, species) [taxon 562], Bifidobacterium bifidum (species) [taxon 1681], Enterococcus (genus) [taxon 1350], Pseudomonas (RNA similarity group I, genus) [taxon 286], Staphylococcus (genus) [taxon 1279], gut metagenome (species) [taxon 749906], Lactobacillus (genus) [taxon 1578], Bacteroides (genus) [taxon 816], Ruminococcus (genus) [taxon 1263], Homo sapiens (human, species) [taxon 9606], Fusobacterium (genus) [taxon 848]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12629333/full.md

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Source: https://tomesphere.com/paper/PMC12629333