# Comparative Analysis of Mucosa-Associated and Luminal Gut Microbiota in Pediatric Ulcerative Colitis

**Authors:** Takeo Kondo, Sonoko Kondo, Haruyuki Nakayama-Imaohji, Ayano Tada, Nafisa Tabassum, Emmanuel Munyeshyaka, Kosuke Koyano, Shinji Nakamura, Takashi Kusaka, Tomomi Kuwahara

PMC · DOI: 10.3390/ijms262110775 · 2025-11-05

## TL;DR

The study compares gut microbiota in children with ulcerative colitis and healthy individuals, finding disrupted microbial patterns linked to disease severity.

## Contribution

The study reveals that pediatric UC patients have a compromised mucous layer allowing mixing of mucosa and luminal microbiota, with specific bacterial markers linked to disease activity.

## Key findings

- Mucosa-associated microbiota in pediatric UC showed homogenous distribution disrupted by disease activity.
- Bacterial groups from the upper digestive tract or environment were more abundant in UC mucosa.
- Lactobacillus and Enterococcus increased, while Faecalibacterium and Blautia decreased in UC mucosa.

## Abstract

Inflammatory bowel diseases (IBD), including ulcerative colitis (UC) and Crohn’s disease, are chronic disorders relating to gut microbiota dysbiosis. Despite severe pancolitis being more prevalent in pediatric UC than in adults, alterations in the colon mucosa-associated microbiota (MAM) and their association with disease severity remain to be elucidated. The present study aimed to compare the gut microbiota in colon lavage fluids (CLFs) and fecal samples from 19 pediatric UC and 19 non-IBD patients. The community structure of MAM inferred by 16S metagenomic analysis was similar throughout the colon regardless of disease type. Bacterial compositions between MAM and feces were significantly different in non-IBD, while no difference was observed in pediatric UC, indicating a compromised mucous layer that could not sufficiently separate the MAM and luminal microbiota in UC. In pediatric UC, homogenous distribution of MAM was gradually disordered with increases in disease activity or mucosal inflammation, and bacterial groups of upper digestive tract or environmental origin were more abundant in MAM. Monitoring key bacterial markers in MAM, which include Lactobacillus and Enterococcus or Faecalibacterium and Blautia as increased or reduced members in pediatric UC, respectively, might be useful for evaluation of patient prognosis.

## Linked entities

- **Diseases:** ulcerative colitis (MONDO:0005101), Crohn’s disease (MONDO:0005011)

## Full-text entities

- **Diseases:** Crohn's disease (MESH:D003424), IBD (MESH:D015212), UC (MESH:D003093), mucosal inflammation (MESH:D007249)
- **Species:** Blautia (genus) [taxon 572511], Faecalibacterium (genus) [taxon 216851], Enterococcus (genus) [taxon 1350], Homo sapiens (human, species) [taxon 9606], Lactobacillus (genus) [taxon 1578]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12610624/full.md

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Source: https://tomesphere.com/paper/PMC12610624