Abstract

Background: Bifidobacterium represents an important early life microbiota member. Specific bifidobacterial components, exopolysaccharides (EPS), positively modulate host responses, with purified EPS also suggested to impact microbe–microbe interactions by acting as a nutrient substrate. Thus, we determined the longitudinal effects of bifidobacterial EPS on microbial communities and metabolite profiles using an infant model colon system. Methods: Differential gene expression and growth characteristics were determined for each strain; Bifidobacterium breve UCC2003 and corresponding isogenic EPS-deletion mutant (B. breve UCC2003del). Model colon vessels were inoculated with B. breve and microbiome dynamics monitored using 16S rRNA sequencing and metabolomics (NMR). Results: Transcriptomics of EPS mutant vs. B. breve UCC2003 highlighted discrete differential gene expression (e.g., eps biosynthetic cluster), though overall growth dynamics between strains were unaffected. The EPS-positive vessel had significant shifts in microbiome and metabolite profiles until study end (405 h); with increases of Tyzzerella and Faecalibacterium, and short-chain fatty acids, with further correlations between taxa and metabolites which were not observed within the EPS-negative vessel. Conclusions: These data indicate that B. breve UCC2003 EPS is potentially metabolized by infant microbiota members, leading to differential microbial metabolism and altered metabolite by-products. Overall, these findings may allow development of EPS-specific strategies to promote infant health.

Highlights

  • Members from the genus Bifidobacterium represent one of the dominant bacterial groups in the early life gut microbiota, with high levels associated with improved infant health [1,2,3,4,5]

  • Pure bacterial cultures were subjected to Transmission Electron Microscopy (TEM) to visualize the presence and absence of EPS prior to model colon experiments

  • Images indicated EPS-positive B. breve UCC2003 bacteria had a thicker and differentially stained cell wall, in contrast to the EPS-negative strain (i.e. B. breve UCC2003del) which is in line with previously published data [16]

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Summary

Introduction

Members from the genus Bifidobacterium represent one of the dominant bacterial groups in the early life gut microbiota, with high levels associated with improved infant health [1,2,3,4,5]. The introduction of solid food at weaning marks a transition into a more complex microbiome, with a concurrent reduction in Bifidobacterium levels, likely due to the loss of milk as a sole dietary source During these phases of significant dietary change, there is a shift in bifidobacterial species and strains, which may link to the wider repertoire of enzymes capable of digesting a more ‘adult’. Conclusions: These data indicate that B. breve UCC2003 EPS is potentially metabolized by infant microbiota members, leading to differential microbial metabolism and altered metabolite by-products. Overall, these findings may allow development of EPS-specific strategies to promote infant health

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