# Lactobacillus paracasei WIS43 alleviates DSS-induced colitis by modulating gut microbiota and suppressing inflammation

**Authors:** Yu Fu, Shuxia Chen, Lei Cui, Ying Cao, Yanan Dong, Yunfeng Duan, Chongming Wu

PMC · DOI: 10.3389/fmicb.2025.1721585 · Frontiers in Microbiology · 2026-01-29

## TL;DR

A new probiotic strain, Lactobacillus paracasei WIS43, shows strong potential in treating ulcerative colitis by reducing inflammation and restoring gut bacteria balance in mice.

## Contribution

Identifies Lactobacillus paracasei WIS43 as a novel probiotic with superior anti-inflammatory and microbiota-modulating effects compared to existing strains.

## Key findings

- WIS43 reduced body weight loss, disease activity, and colon shortening in a mouse model of colitis.
- The strain significantly lowered inflammatory markers like TNF-α, IL-6, and IL-1β.
- WIS43 restored beneficial gut bacteria and outperformed a commercial Lactobacillus strain in anti-inflammatory activity.

## Abstract

Ulcerative colitis (UC) is a chronic inflammatory disorder of the colon with rising incidence and limited therapeutic options. Probiotics are increasingly recognized as potential interventions, but strain-specific differences remain insufficiently defined.

We conducted a meta-analysis of publicly available microbiome datasets to characterize disease-associated dysbiosis, focusing on the genus Lactobacillus. We then evaluated Lactobacillus paracasei WIS43, a novel strain isolated from the breast milk of a healthy volunteer, in a dextran sulfate sodium (DSS)-induced murine colitis model, using mesalazine and the commercial strain Lactobacillus paracasei LPC-37 as comparators. Disease severity, histopathology, inflammatory cytokines, and gut microbiota composition were systematically assessed.

Meta-analysis confirmed a significant depletion of Lactobacillus in UC patients. In vivo, WIS43 treatment reduced body weight loss, disease activity index scores, and colon shortening. Histological analysis revealed preserved epithelial integrity and reduced inflammatory infiltration. WIS43 significantly decreased serum and colonic TNF-α, IL-6, and IL-1β levels, demonstrating stronger anti-inflammatory activity than LPC-37 and comparable efficacy to mesalazine. 16S rRNA sequencing further showed that WIS43 restored beneficial taxa, including Lactobacillus johnsonii and Lactobacillus taiwanensis, while reducing potentially pathogenic bacteria.

These findings identify WIS43 as a promising probiotic candidate for the prevention and treatment of UC, supporting its therapeutic potential through coordinated modulation of host immunity and gut microbiota.

Infographic explaining the impact of probiotic WIS43 on ulcerative colitis (UC) and dysbiosis. It shows improved clinical symptoms, restored gut structure, potent anti-inflammatory effects, and a rebalanced microbiome. Probiotics are isolated from breast milk, specifically L. paracasei WIS43. Experimental results in mice indicate reduced body weight loss and colon shortening, preserved epithelium, reduced inflammation, and increased beneficial microbiota. Concludes with WIS43 as a promising therapeutic for UC, emphasizing modulation of host immunity and gut microbiota balance.

## Linked entities

- **Chemicals:** mesalazine (PubChem CID 4075), IL-6 (PubChem CID 165368475)
- **Diseases:** ulcerative colitis (MONDO:0005101)
- **Species:** Lactobacillus johnsonii (taxon 33959), Lactobacillus taiwanensis (taxon 508451)

## Full-text entities

- **Diseases:** inflammatory disorder of the colon (MESH:D003108), UC (MESH:D003093), inflammation (MESH:D007249), dysbiosis (MESH:D064806), colitis (MESH:D003092), weight loss (MESH:D015431)
- **Chemicals:** DSS (MESH:D016264), mesalazine (MESH:D019804), LPC-37 (-)
- **Species:** Lacticaseibacillus paracasei (species) [taxon 1597], Mus musculus (house mouse, species) [taxon 10090], Lactobacillus johnsonii (species) [taxon 33959], Lactobacillus taiwanensis (species) [taxon 508451], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12900382/full.md

## References

69 references — full list in the complete paper: https://tomesphere.com/paper/PMC12900382/full.md

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Source: https://tomesphere.com/paper/PMC12900382