Proteobacteria abundance during nursing predicts physical growth and brain volume at one year of age in young rhesus monkeys. Issue 6 (27th May 2021)

• Record Type: Journal Article
• Authors: Rendina, Danielle N.; Lubach, Gabriele R.; Lyte, Mark; Phillips, Gregory J.; Gosain, Ankush; Pierre, Joseph F.; Vlasova, Roza M.; Styner, Martin A.; Coe, Christopher L.
• Is Part Of: FASEB journal. Volume 35:Issue 6(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-05-27
• Subjects: breast feeding -- gut microbiome -- infant development -- neuroimaging -- Proteobacteria; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.202002162R
• Languages: English
• ISSNs: 0892-6638

Abstract

Abstract: Over the last decade, multiple studies have highlighted the essential role of gut microbiota in normal infant development. However, the sensitive periods during which gut bacteria are established and become associated with physical growth and maturation of the brain are still poorly defined. This study tracked the assembly of the intestinal microbiota during the initial nursing period, and changes in community structure after transitioning to solid food in infant rhesus monkeys ( Macaca mulatta ). Anthropometric measures and rectal swabs were obtained at 2‐month intervals across the first year of life and bacterial taxa identified by 16S rRNA gene sequencing. At 12 months of age, total brain and cortical regions volumes were quantified through structural magnetic resonance imaging. The bacterial community structure was dynamic and characterized by discrete maturational phases, reflecting an early influence of breast milk and the later transition to solid foods. Commensal microbial taxa varied with diet similar to findings in other animals and human infants; however, monkeys differ in the relative abundances of Lactobacilli and Bifidobacteria, two taxa predominant in breastfed human infants. Higher abundances of taxa in the phylum Proteobacteria during nursing were predictive of slower growth trajectories and smaller brain volumes at one year of age. Our findings define discrete phases of microbial succession in infant monkeys and suggest there may be a critical period during nursing when endogenous differences in certain taxa can shift the community structure and influence the pace of physical growth and the maturational trajectory of the brain.