Gut Microbiome

Fecal fermentation of human ileal fluid after mango intake impacts on colonic microbiota and microbial (poly)phenol catabolism.

TL;DR

Ileal fluid enriched with mango (poly)phenols undergoes substantial microbial catabolism during ex vivo fecal fermentation, with the IF matrix rather than mango (poly)phenols per se significantly influencing gut bacterial diversity and SCFA production, while characteristic catabolites positively correlate with commensal and healthy-related bacteria.

Key Findings

A total of 48 phenolic compounds were identified in fermented ileal fluid samples before and after mango consumption.

  • Compounds were identified using UHPLC-HRMS analysis
  • Main compound classes included benzoic acids, hydroxybenzenes, and galloyl derivatives
  • High interindividual variability was observed across the six ileostomist participants
  • Samples were analyzed at pre-fermentation (0 h) and post-fermentation (2, 6, and 24 h) timepoints

Three compounds emerged as possible discriminants of fermented mango ileal fluid samples: 3,4,5-trihydroxybenzoic acid, 3,5-dihydroxy-4-methoxybenzoic acid, and 1,3,5-trihydroxybenzene.

  • These compounds were identified as microbial catabolites
  • They were distinguished from fermented control (pre-mango) ileal fluid samples
  • Identification was performed by UHPLC-HRMS
  • These galloyl-derived catabolites reflect microbial transformation of mango (poly)phenols in colonic conditions

The ileal fluid matrix, rather than mango (poly)phenols themselves, significantly influenced gut bacterial alpha-diversity.

  • Statistical significance was reported at p < 0.05 for alpha-diversity
  • 16S rRNA gene sequencing was used to assess changes in gut microbiota
  • Six ileostomist participants provided ileal fluids collected before and for an 8 h period after mango consumption
  • Ex vivo fecal fermentation was used to simulate colonic conditions

The ileal fluid matrix significantly increased microbial short-chain fatty acid (SCFA) production, primarily acetic, butyric, and propionic acids.

  • SCFAs were measured by GC-FID
  • The three main SCFAs produced were acetic, butyric, and propionic acids
  • The effect was attributed to the IF matrix rather than mango (poly)phenols specifically
  • SCFA production was monitored across fermentation timepoints of 0, 2, 6, and 24 h

A significant positive correlation was found between characteristic mango (poly)phenol catabolites in fermented ileal fluid samples and commensal and health-related bacteria including Bifidobacterium spp.

  • Correlation was statistically significant at p < 0.05
  • Bifidobacterium spp. was specifically identified as positively correlated with characteristic catabolites
  • The correlation involved commensal and 'healthy-related bacteria'
  • High interindividual variability was noted across participants despite these correlations

Ileal fluids were collected from six ileostomist participants before and for 8 hours after mango consumption and subjected to ex vivo fecal fermentation.

  • The study was registered at clinicaltrials.gov as NCT06182540
  • Ileostomists were used as a model to collect ileal fluid that would normally reach the colon
  • Collection period was 8 h post-mango consumption
  • Ex vivo fermentation timepoints were 0, 2, 6, and 24 h

Mango comprises a rich source of (poly)phenolic compounds, predominantly galloyl-derived (poly)phenols, a portion of which are metabolised and absorbed in the upper gastrointestinal tract while the remainder reach the colon.

  • Mangifera indica L. was the mango species studied
  • Galloyl-derived (poly)phenols are the predominant class in mango
  • Bioactive compounds not absorbed in the upper GI tract are subjected to microbial catabolism in the colon
  • The ileostomist model was used to capture the fraction reaching the colon

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Citation

C&#xe1;ceres-Jim&#xe9;nez S, Molinero N, Cueva C, Dobani S, Pourshahidi K, Gill C, et al.. (2026). Fecal fermentation of human ileal fluid after mango intake impacts on colonic microbiota and microbial (poly)phenol catabolism.. Food research international (Ottawa, Ont.). https://doi.org/10.1016/j.foodres.2025.117217