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Breast-Milk Lactobacillus Gasseri FN136 Alleviates DSS-Induced Ulcerative Colitis Through Microbiota-Independent
Qingcui Li1, Wenhao Wang1, Fan Zhou1
1Institute of Nutrition and Health, Qingdao University, Qingdao, 266071, China.
Probiotics and Antimicrobial Proteins
|November 28, 2025
Summary
Lactobacillus gasseri FN136, a probiotic, effectively reduced ulcerative colitis (UC) symptoms in a DSS-induced model. It works via a postbiotic-host pathway, not by altering gut microbiota composition.
Area of Science:
- Microbiology
- Immunology
- Gastroenterology
Background:
- Ulcerative colitis (UC) is a chronic inflammatory condition of the colon with increased colorectal cancer risk.
- Probiotics are explored as adjunctive therapies for UC management.
Purpose of the Study:
- To evaluate the efficacy of Lactobacillus gasseri FN136, a breast-milk-derived probiotic, as an intervention for ulcerative colitis.
- To elucidate the mechanism of action of FN136 in mitigating colitis.
Main Methods:
- In vitro assessment of FN136's anti-inflammatory properties, tolerance, and antimicrobial activity.
- In vivo study using a DSS-induced colitis model in mice, with daily oral administration of FN136.
- Analysis of serum markers, immune cell populations, colonic histology, and systemic inflammation markers.
- 16S rRNA sequencing to assess changes in gut microbial composition.
Main Results:
- FN136 demonstrated in vitro anti-inflammatory properties and tolerance.
- In vivo, FN136 significantly attenuated DSS-induced UC, reducing disease activity, weight loss, and colonic damage.
- FN136 restored serum L-arginine, increased splenic regulatory T cells, and elevated nitric oxide production.
- Systemic inflammation markers (IL-6, MPO, LPS, FITC-dextran) were significantly reduced.
- No significant alterations in global microbial composition were observed via 16S rRNA sequencing.
Conclusions:
- Lactobacillus gasseri FN136 mitigates DSS-induced UC through a microbiota-independent postbiotic-host axis.
- FN136 restores serum arginine and enhances immune-barrier homeostasis, offering a novel approach for UC intervention.
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