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. 2022 Feb 21;12(1):2875.
doi: 10.1038/s41598-022-06792-6.

Maternal anthropometric variables and clinical factors shape neonatal microbiome

Affiliations

Maternal anthropometric variables and clinical factors shape neonatal microbiome

Riccardo Farinella et al. Sci Rep. .

Abstract

Recent studies indicate the existence of a complex microbiome in the meconium of newborns that plays a key role in regulating many host health-related conditions. However, a high variability between studies has been observed so far. In the present study, the meconium microbiome composition and the predicted microbial metabolic pathways were analysed in a consecutive cohort of 96 full-term newborns. The effect of maternal epidemiological variables on meconium diversity was analysed using regression analysis and PERMANOVA. Meconium microbiome composition mainly included Proteobacteria (30.95%), Bacteroidetes (23.17%) and Firmicutes (17.13%), while for predicted metabolic pathways, the most abundant genes belonged to the class "metabolism". We observed a significant effect of maternal Rh factor on Shannon and Inverse Simpson indexes (p = 0.045 and p = 0.049 respectively) and a significant effect of delivery mode and maternal antibiotic exposure on Jaccard and Bray-Curtis dissimilarities (p = 0.001 and 0.002 respectively), while gestational age was associated with observed richness and Shannon indexes (p = 0.018 and 0.037 respectively), and Jaccard and Bray-Curtis dissimilarities (p = 0.014 and 0.013 respectively). The association involving maternal Rh phenotype suggests a role for host genetics in shaping meconium microbiome prior to the exposition to the most well-known environmental variables, which will influence microbiome maturation in the newborn.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1
Figure 1
Box plots of alpha diversity by maternal Rh factor. The three panels (a), (b) and (c) report the observed richness index, Shannon index and Inverse Simpson index respectively.
Figure 2
Figure 2
Ordination plot for the first two principal coordinates based on Bray–Curtis (upper plots) and Jaccard (lower plots) dissimilarities reported by, from left to right, maternal antibiotic exposure (a, d), delivery mode (b, e) and gestational age (c, f). For simplicity of graphical representation, gestational age is reported using quartiles.

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