Bifidobacterium breve UCC2003 Exopolysaccharide Modulates the Early Life Microbiota by Acting as a Potential Dietary Substrate

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 eff...

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Veröffentlicht in:Nutrients 2020-03, Vol.12 (4), p.948
Hauptverfasser: Püngel, Deborah, Treveil, Agatha, Dalby, Matthew J, Caim, Shabhonam, Colquhoun, Ian J, Booth, Catherine, Ketskemety, Jennifer, Korcsmaros, Tamas, van Sinderen, Douwe, Lawson, Melissa Ae, Hall, Lindsay J
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container_issue 4
container_start_page 948
container_title Nutrients
container_volume 12
creator Püngel, Deborah
Treveil, Agatha
Dalby, Matthew J
Caim, Shabhonam
Colquhoun, Ian J
Booth, Catherine
Ketskemety, Jennifer
Korcsmaros, Tamas
van Sinderen, Douwe
Lawson, Melissa Ae
Hall, Lindsay J
description 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. Differential gene expression and growth characteristics were determined for each strain; UCC2003 and corresponding isogenic EPS-deletion mutant ( UCC2003del). Model colon vessels were inoculated with and microbiome dynamics monitored using 16S rRNA sequencing and metabolomics (NMR). Transcriptomics of EPS mutant vs. UCC2003 highlighted discrete differential gene expression (e.g., 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 and , and short-chain fatty acids, with further correlations between taxa and metabolites which were not observed within the EPS-negative vessel. These data indicate that 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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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. Differential gene expression and growth characteristics were determined for each strain; UCC2003 and corresponding isogenic EPS-deletion mutant ( UCC2003del). Model colon vessels were inoculated with and microbiome dynamics monitored using 16S rRNA sequencing and metabolomics (NMR). Transcriptomics of EPS mutant vs. UCC2003 highlighted discrete differential gene expression (e.g., 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 and , and short-chain fatty acids, with further correlations between taxa and metabolites which were not observed within the EPS-negative vessel. These data indicate that UCC2003 EPS is potentially metabolized by infant microbiota members, leading to differential microbial metabolism and altered metabolite by-products. 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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. Differential gene expression and growth characteristics were determined for each strain; UCC2003 and corresponding isogenic EPS-deletion mutant ( UCC2003del). Model colon vessels were inoculated with and microbiome dynamics monitored using 16S rRNA sequencing and metabolomics (NMR). Transcriptomics of EPS mutant vs. UCC2003 highlighted discrete differential gene expression (e.g., biosynthetic cluster), though overall growth dynamics between strains were unaffected. 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subjects Babies
Bifidobacterium breve
Bifidobacterium breve - genetics
Bifidobacterium breve - growth & development
Bifidobacterium breve - physiology
Breastfeeding & lactation
Colon
Colon - metabolism
Colon - microbiology
Deletion mutant
Dietary Supplements
Ethanol
Exopolysaccharides
Gastrointestinal Microbiome - physiology
Gene Expression
Genomes
Host Microbial Interactions - physiology
Humans
Infant
Infant Health
Infants
Metabolism
Metabolites
Metabolomics
Microbial activity
Microbiomes
Microbiota
Microorganisms
Mutants
Mutation
Polysaccharides, Bacterial - genetics
Polysaccharides, Bacterial - metabolism
RNA, Ribosomal, 16S - genetics
rRNA 16S
Substrates
Transcriptomics
title Bifidobacterium breve UCC2003 Exopolysaccharide Modulates the Early Life Microbiota by Acting as a Potential Dietary Substrate
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