In vitro gut microbiome response to carbohydrate supplementation is acutely affected by a sudden change in diet

BMC Microbiol. 2023 Jan 28;23(1):32. doi: 10.1186/s12866-023-02776-2.

Abstract

Background: Interactions between diet, stress and the gut microbiome are of interest as a means to modulate health and performance. Here, in vitro fermentation was used to explore the effects of a sudden change in diet, 21 days sole sustenance on the Meal, Ready-to-Eat (MRE) U.S. military combat ration, on inter-species competition and functional potential of the human gut microbiota. Human fecal samples collected before and after MRE intervention or consuming a habitual diet (HAB) were introduced to nutrient-rich media supplemented with starch for in vitro fermentation under ascending colon conditions. 16S rRNA amplicon and Whole-metagenome sequencing (WMS) were used to measure community composition and functional potential. Specific statistical analyses were implemented to detect changes in relative abundance from taxa, genes and pathways.

Results: Differential changes in relative abundance of 11 taxa, Dorea, Lachnospira, Bacteroides fragilis, Akkermansia muciniphila, Bifidobacterium adolescentis, Betaproteobacteria, Enterobacteriaceae, Bacteroides egerthii, Ruminococcus bromii, Prevotella, and Slackia, and nine Carbohydrate-Active Enzymes, specifically GH13_14, over the 24 h fermentation were observed as a function of the diet intervention and correlated to specific taxa of interest.

Conclusions: These findings suggest that consuming MRE for 21 days acutely effects changes in gut microbiota structure in response to carbohydrate but may induce alterations in metabolic capacity. Additionally, these findings demonstrate the potential of starch as a candidate supplemental strategy to functionally modulate specific gut commensals during stress-induced states.

Trial registration: ClinicalTrials.gov NCT02423551.

Keywords: Carbohydrate metabolism; Carbohydrate-active enzymes; Gut microbiome; Gut microbiota; In vitro fermentation; Meal Ready-to-Eat (MRE); Metabolic competition; Microbial ecology; Microbial functional potential; Next generation sequencing.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Carbohydrates
  • Diet
  • Dietary Supplements
  • Feces / microbiology
  • Gastrointestinal Microbiome* / genetics
  • Humans
  • RNA, Ribosomal, 16S / genetics
  • Starch / metabolism

Substances

  • RNA, Ribosomal, 16S
  • Carbohydrates
  • Starch

Associated data

  • ClinicalTrials.gov/NCT02423551