Comparative characterization of the infant gut microbiome and their maternal lineage by a multi-omics approach.
Tomás Clive Barker-TejedaElisa Zubeldia-VarelaAndrea Macías-CameroLola AlonsoIsabel Adoración Martín-AntonianoMaría Fernanda Rey-StolleLeticia Mera-BerriatuaRaphaëlle BazirePaula Cabrera-FreitagMeera ShanmuganathanPhilip Britz-MckibbinCarles UbedaMaría Pilar FrancinoDomingo BarberMaría Dolores Ibáñez-SandínCoral BarbasMarina Pérez-GordoAlma VillaseñorPublished in: Nature communications (2024)
The human gut microbiome establishes and matures during infancy, and dysregulation at this stage may lead to pathologies later in life. We conducted a multi-omics study comprising three generations of family members to investigate the early development of the gut microbiota. Fecal samples from 200 individuals, including infants (0-12 months old; 55% females, 45% males) and their respective mothers and grandmothers, were analyzed using two independent metabolomics platforms and metagenomics. For metabolomics, gas chromatography and capillary electrophoresis coupled to mass spectrometry were applied. For metagenomics, both 16S rRNA gene and shotgun sequencing were performed. Here we show that infants greatly vary from their elders in fecal microbiota populations, function, and metabolome. Infants have a less diverse microbiota than adults and present differences in several metabolite classes, such as short- and branched-chain fatty acids, which are associated with shifts in bacterial populations. These findings provide innovative biochemical insights into the shaping of the gut microbiome within the same generational line that could be beneficial in improving childhood health outcomes.
Keyphrases
- mass spectrometry
- capillary electrophoresis
- gas chromatography
- single cell
- liquid chromatography
- high performance liquid chromatography
- high resolution mass spectrometry
- fatty acid
- tandem mass spectrometry
- high resolution
- endothelial cells
- genome wide
- birth weight
- genetic diversity
- weight gain
- early life
- simultaneous determination
- pregnancy outcomes
- young adults
- pregnant women
- genome wide analysis
- childhood cancer