Stress-related disorders pose a major health problem, and those that involve social components are particularly problematic due to the necessity of a social structure for an ideal quality of life. Vulnerability to fear-related disorders such as post-traumatic stress disorder (PTSD) and social anxiety disorder (SAD) is enhanced in individuals with histories of early life adversity (Maercker et al., 2013). Early emotional neglect (Solomon & Mikulincer, 2007) and early social adversity are particularly potent risk factors for anxiety disorders including SAD (Kertz, Sylvester, Tillman, & Luby, 2017). Social fear can profoundly and persistently impair the quality of an individual's functioning across many domains, as social interactions are a vital component of almost every aspect of life (Herman, 1992; Karatzias et al., 2017).
Purpose
Exclusive breastfeeding promotes gut microbial compositions associated with lower rates of metabolic and autoimmune diseases. Its cessation is implicated in increased microbiome-metabolome discordance, suggesting a vulnerability to dietary changes. Formula supplementation is common within our low-income, ethnic-minority community. We studied exclusively breastfed (EBF) neonates’ early microbiome-metabolome coupling in efforts to build foundational knowledge needed to target this inequality.
Methods
Maternal surveys and stool samples from seven EBF neonates at first transitional stool (0–24 hours), discharge (30–48 hours), and at first appointment (days 3–5) were collected. Survey included demographics, feeding method, medications, medical history and tobacco and alcohol use. Stool samples were processed for 16S rRNA gene sequencing and lipid analysis by gas chromatography-mass spectrometry. Alpha and beta diversity analyses and Procrustes randomization for associations were carried out.
Results
Firmicutes, Proteobacteria, Bacteroidetes and Actinobacteria were the most abundant taxa. Variation in microbiome composition was greater between individuals than within (
p
=0.001). Palmitic, oleic, stearic, and linoleic acids were the most abundant lipids. Variation in lipid composition was greater between individuals than within (
p
=0.040). Multivariate composition of the metabolome, but not microbiome, correlated with time (
p
=0.030). Total lipids, saturated lipids, and unsaturated lipids concentrations increased over time (
p
=0.012,
p
=0.008,
p
=0.023). Alpha diversity did not correlate with time (
p
=0.403). Microbiome composition was not associated with each samples’ metabolome (
p
=0.450).
Conclusion
Neonate gut microbiomes were unique to each neonate; respective metabolome profiles demonstrated generalizable temporal developments. The overall variability suggests potential interplay between influences including maternal breastmilk composition, amount consumed and living environment.
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