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

2026-01-29
Frontiers in microbiology 16

PubMed: 41695140
DOI: 10.3389/fmicb.2025.1721585

Study Design

Type: Meta-Analysis
Population: UC patients; a dextran sulfate sodium (DSS)-induced murine colitis model
Methods: 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 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.

Introduction

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.

Methods

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.

Results

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.

Conclusion

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.

Research Insights

Supplement	Dose	Health Outcome	Effect Type	Effect Size	Source
Lacticaseibacillus paracasei Lpc-37	—	Modulated Gut Microbiota	Beneficial	Moderate	View source 16S rRNA sequencing further showed that WIS43 restored beneficial taxa... while reducing potentially pathogenic bacteria
Lacticaseibacillus paracasei Lpc-37	—	Reduced Colitis Severity	Beneficial	Moderate	View source WIS43 treatment reduced body weight loss, disease activity index scores, and colon shortening... demonstrating stronger anti-inflammatory activity than LPC-37
Lacticaseibacillus paracasei Lpc-37	—	Reduced Inflammation	Beneficial	Moderate	View source WIS43 significantly decreased serum and colonic TNF-α, IL-6, and IL-1β levels, demonstrating stronger anti-inflammatory activity than LPC-37
Lactobacillus paracasei	—	Improved Gut Microbiota Composition	Beneficial	Moderate	View source 16S rRNA sequencing further showed that WIS43 restored beneficial taxa, including Lactobacillus johnsonii and Lactobacillus taiwanensis, while reducing potentially pathogenic bacteria.
Lactobacillus paracasei	—	Reduced Inflammation	Beneficial	Moderate	View source WIS43 significantly decreased serum and colonic TNF-α, IL-6, and IL-1β levels, demonstrating stronger anti-inflammatory activity than LPC-37
Lactobacillus paracasei	—	Reduced Ulcerative Colitis Symptoms	Beneficial	Moderate	View source WIS43 treatment reduced body weight loss, disease activity index scores, and colon shortening. Histological analysis revealed preserved epithelial integrity and reduced inflammatory infiltration.