Project description:The objective of the present study was to identify the nutrient utilization and the SCFA production potential of gut microbes during the first year of life. The 16S sequencing data represents 100 mother-child pairs, longitudinally for the infants (0, 3mo, 6mo and 12mo) and mothers 18 weeks pregnancy. We wanted to identify the SCFA composition in pregnant woman and their infants through the first year of life, and their correlation to gut bacteria and other influencal factors. Metaproteomics on selected infants were analyzed to look for nutrient sources used by potential SCFA producers.
Project description:<p>Infancy is a critical period for the colonization of the gut microbiome. However, xenobiotic effects on gut microbiome development in early life remain poorly understood. Here, we recruit 146 mother-infant pairs and collect stool samples at 3, 6, and 12 months after delivery for amplicon sequencing (N = 353), metagenomics (N = 65), and metabolomics (N = 198). Trace elements in maternal hair samples (N = 119) affect the alpha diversity of the infant gut microbiome. Shannon diversity in 3-month-old infants is correlated positively with selenium and negatively with copper, and the relative abundance of Bifidobacterium increases under high exposure to aluminum and manganese. During the first year of life, infants and their paired mothers have distinct microbial diversity and composition, and their bacterial community structures gradually approach. There are 56 differential metabolites between the first and second postpartum visits and 515 differential metabolites between the second and third visits. The typical profile of antibiotic resistance genes (ARGs) differs significantly between infants and their mothers. High copper and arsenic exposure may induce the enrichment of ARGs in the infant gut. Our findings highlight the dynamics of the gut microbiome, metabolites, and ARG profiles of mother-infant pairs after delivery, associated with prenatal exposure to trace elements.</p>
Project description:Fecal samples collected from mothers and their infants (United States). Mothers received antibiotics based on clinical indication or served as untreated controls. Untargeted LC-MS/MS acquisition was performed on a Vanquish ultra-high-performance liquid chromatography (UHPLC) system coupled to a QExactive Orbitrap (Thermo Scientific) mass spectrometer.
Project description:Blood collected from infants at week 6 and week 7 of life to profile how the transcriptome is changed following routine early life vaccination. Paired faecal metagenomic data is available for these infants under BioProject PRJNA807448 at the Sequence Read Archive.
Project description:<p>Background: Disturbances in the gut microbiome (GM) during the first year of life may contribute to allergy risk. This period is characterized by rapid microbial colonization, influenced by factors like delivery mode and infant feeding practices. This study investigates changes in key GM taxa and fecal metabolites in relation to allergy development, delivery mode, age and infant feeding practices during the first year of life.</p><p><br></p><p>Methods: In this study, 72 infants, exclusively breastfed for at least 16 weeks and at risk of developing allergies, were followed in their first year during which allergy manifestations were recorded and fecal samples were collected. The samples were subjected to metabolic profiling covering host and microbial metabolites and fluorescent in situ hybridization to quantify <em>Bifidobacterium </em>spp. and the <em>Eubacterium rectale</em>/<em>Clostridium coccoides</em> group.</p><p><br></p><p>Results: Strong age-associated metabolic shifts were observed, particularly in aromatic amino acid metabolites, bile acids, B vitamins and short and long-chain fatty acids. Introduction of complementary feeding and the cessation of breastfeeding were significantly associated with changes to the fecal metabolome. Delivery mode had a pronounced impact on the metabolome, with differences persisting until 6 months of age. Infants who developed an allergy (n=20) had lower <em>Bifidobacterium </em>spp. and higher long-chain fatty acid levels before age of 16 weeks.</p><p><br></p><p>Conclusion: This study offers valuable insights into the longitudinal development of the fecal metabolome during infancy. It highlights potential early biomarkers for allergy risk, which could inform future dietary strategies to support gut health and reduce the risk of developing allergy.</p>
Project description:The prevalence of atopic diseases has increased with atopic dermatitis (AD) as the earliest manifestation. We assessed if molecular risk factors in atopic mothers influence their offsprings’ susceptibility to an atopic disease. Pairs of pregnant women and their infants with or without parental atopy were followed over the first 2 years of life. Global DNA methylation and differentially methylated regions (DMR) were determined in atopic and non-atopic mothers. During the first 2 years of life, AD was more prevalent in children of atopic compared to non-atopic mothers with an increase in food sensitization in children with AD. 165 DMRs distinguished atopic from non-atopic mothers. Maternal atopy combined with DMRs increased the offsprings’ predicted risk to develop AD from an odds ratio of 2.56 to 4.26.