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Updated: May 5, 2026

DNBS/TNBS Colitis Models: Providing Insights Into Inflammatory Bowel Disease and Effects of Dietary Fat
Published on: February 27, 2014
Recombinant MAM from Faecalibacterium duncaniae exhibits a protective effect in DNBS-induced colitis
Thaís Vilela Rodrigues1,2, Luís Lima de Jesus1,2, Monique Ferrary Américo1,2
1Instituto de Ciências Biológicas, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
We purified a microbial anti-inflammatory molecule (MAM) from Faecalibacterium duncaniae A2-165 and demonstrated its direct anti-inflammatory effects in vitro and in a colitis model. This validates MAM
Area of Science:
- Gut microbiota and immunology
- Probiotic research and development
- Inflammatory Bowel Disease (IBD) therapeutics
Background:
- Faecalibacterium duncaniae A2-165 is a next-generation probiotic linked to IBD.
- Microbial anti-inflammatory molecule (MAM) is a key effector of F. duncaniae A2-165.
- Direct anti-inflammatory effects of purified MAM have not been previously evaluated.
Purpose of the Study:
- To produce and purify recombinant MAM (R-MAM).
- To evaluate the direct anti-inflammatory activity of R-MAM in vitro.
- To assess the protective effects of R-MAM in a murine model of intestinal inflammation.
Main Methods:
- Recombinant MAM (R-MAM) was produced and purified under denaturing conditions.
- In vitro assays were conducted using human intestinal epithelial cells (HT-29) and peripheral blood mononuclear cells (PBMCs).
- A DNBS-induced colitis murine model was used to evaluate in vivo efficacy.
Main Results:
- Purified R-MAM induced an anti-inflammatory cytokine profile in vitro.
- Oral administration of R-MAM significantly prevented weight loss in a colitis model.
- R-MAM reduced colon weight and thickness, indicating reduced inflammation.
Conclusions:
- The study validates the therapeutic potential of MAM for intestinal inflammation.
- R-MAM demonstrated direct anti-inflammatory activity despite purification under denaturing conditions.
- Future research should focus on optimizing protein stability for enhanced therapeutic efficacy.
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