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Gut Microbiome Composition and Metabolic Capacity Differ by FUT2 Secretor Status in Exclusively Breastfed Infants
Alexander W Thorman1, Grace Adkins2, Shannon C Conrey1,3
1Department of Environmental and Public Health Sciences, Division of Epidemiology, University of Cincinnati College of Medicine, Cincinnati, OH 45220, USA.
Nutrients
|January 21, 2023
Summary
Infant secretor status, determined by the fucosyltransferase2 (FUT2) gene, significantly impacts the gut microbiome of breastfed infants. This influences microbial diversity, enterotypes, and metabolic functions, highlighting infant genetics over maternal factors.
Area of Science:
- Microbiome research
- Human genetics
- Infant nutrition
Background:
- The fucosyltransferase2 (FUT2) gene polymorphism affects gut disease risk.
- Secretor individuals have fucosylated mucosa, supporting gut bacteria.
- Maternal secretor status influences milk oligosaccharides, but infant impact was unknown.
Purpose of the Study:
- To investigate the impact of maternal and infant secretor status on the early infant fecal microbiome.
- To determine if infant FUT2 genotype or phenotype is more influential on the infant microbiome.
Main Methods:
- Analysis of fecal microbiome samples from 59 exclusively breastfed 2-month-old infants.
- Measurement of maternal and infant secretor status via FUT2 genotype and phenotype.
- Comparison of microbiome alpha diversity, enterotypes, and metabolic pathways based on secretor status.
Main Results:
- Infant secretor status, not maternal, strongly associated with infant microbiome composition.
- Higher alpha diversity observed in full-secretor infants compared to low- or non-secretors.
- Distinct microbial enterotypes linked to infant secretor phenotype, including Bifidobacterium dominance.
Conclusions:
- Infant secretor status is a key determinant of early gut microbial colonization and metabolic capacity in breastfed infants.
- FUT2 genotype and phenotype in infants play a crucial role in shaping their developing microbiome.
- Maternal secretor status has a lesser impact on the infant microbiome compared to infant's own status.
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