Nursery Peers Rival Family in Shaping the Infant Gut Microbiome
Source PublicationNature
Primary AuthorsRicci, Heidrich, Punčochář et al.

Babies attending nursery exchange gut bacteria so frequently that peer-acquired strains rival those inherited from family within a single term. Historically, accurately mapping these transfers was a logistical nightmare. Researchers struggled to distinguish between generic species presence and the movement of specific biological strains, often relying on assumptions rather than hard data.
These results were observed under controlled laboratory conditions, so real-world performance may differ.
Methodological Shifts in Analysing the Infant Gut Microbiome
The validity of these findings rests entirely on the shift from older sequencing techniques to high-resolution metagenomics. Previous reliance on 16S rRNA gene markers offered a blurry snapshot. It identified who was there taxonomically but lacked the resolution to track specific strain movements. It is akin to knowing someone named 'Smith' entered the room, without knowing which Smith. The current study utilises dense longitudinal sampling. By analysing the specific genomic composition—relying on distinct signatures like GC content variations and single-nucleotide polymorphisms (SNPs) within strains—researchers can now fingerprint specific microbes. This allows for the definitive tracking of a single strain jumping from one infant to another, rather than assuming independent colonisation by the same species.
The Impact of Antibiotics and Siblings
The study tracked 134 individuals across three facilities, analysing over 1,000 faecal samples. The data indicates that baby-to-baby transmission is not merely incidental; it is systemic. By the end of the first term, the proportion of the infant gut microbiome derived from nursery peers was comparable to that derived from family members. However, the context of this colonisation varies.
Antibiotic treatment appeared to be the most significant factor facilitating the influx of new strains. This suggests that when the established flora is disrupted, the gut becomes an open door for peer-associated microbes. Conversely, having siblings offered a protective effect. Infants with brothers or sisters exhibited higher baseline diversity and acquired fewer strains from their nursery peers. This implies that a niche saturation effect may occur; the gut is already populated by sibling-shared microbes, leaving less room for nursery invaders.
While the study effectively measures the flux of bacteria, it does not confirm the long-term health implications of this exchange. We observe that transmission happens. We do not yet know if this 'socialising' of the microbiome benefits immune development or merely increases the burden of potential pathogens.