Analysis of human colostrum reveals differential co-occurrence networks of metabolites, microbiota, and cytokines in maternal obesity
July Stephany Gámez-ValdeziD, Karina Corona-CervantesiD, Erick Saúl Sánchez-SalgueroiD, Mario René Alcorta-GarcíaiD, Claudia N. López-VillaseñoriD, Rommel A. Carballo-CastañedaiD, Aldo Moreno‐UlloaiD, Victor Javier Lara DíaziD, Marion E. G. BrunckiD, Cuauhtémoc Licona‐CassaniiD
Abstract
Breastmilk is essential for neonatal development, particularly in seeding the gut microbiota and modulating the maturing immune system. This proof-of-concept study explores the systemic nature of colostrum and the influence of maternal obesity on co-occurrences of colostrum bioactives. Using 16S-rRNA sequencing, untargeted metabolomics, and cytokines quantification, we analyzed co-occurring elements in the colostrum of mothers with normal weight (18.5 30). We identified 5 different co-occurrence networks, characterized by positive correlations of taxonomically related bacteria. Our integrative analysis reveals that Aeromonadaceae, Xanthomonadaceae and Staphylococcaceae negatively correlate with proinflammatory cytokines TNF-, IL-6, and IL-12p70 in the colostrum of mothers with obesity (WO). Additionally, lipid mediators, including 15-HEDE and LysoPC(16:00), were associated with cytokines IL-10 and IL-8, and microbiota taxa Burkholderiaceae, Beijerinckiaceae and Planococcaceae-firstly reported in colostrum from mothers WO. Our findings suggest a pervasive regulation of bioactives in the colostrum of mothers WO. This may have implications for a distinctive neonatal intestine development.
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