Abstract

ABSTRACTAkkermansia muciniphila has been proved to play a crucial role in the progression of colitis, but its underlying mechanism remains inconclusive. In this study, we aim to investigate the effect of A. muciniphila on the development of acute colitis and explore the underlying mechanism. We found that the fecal level of A. muciniphila was decreased in ulcerative colitis (UC) patients compared to the healthy people in the GMrepo database. Oral administration of A. muciniphila strain BAA-835 significantly ameliorated the symptoms in dextran sulfate sodium (DSS)-induced acute colitis, evidenced by decreased body weight loss, colon length shortening, and colon histological inflammatory score. In addition, the number of goblet cells and the mucin family were enhanced after A. muciniphila treatment. Furthermore, proinflammatory cytokines such as tumor necrosis factor alpha (TNF-α), interleukin-6 (IL-6), and monocyte chemoattractant protein 1 (MCP-1) had a downward trend. Mechanistically, the expression of NLRP3, caspase-1 p20, and IL-1β p17 were upregulated in A. muciniphila-treated mice. Additionally, the colon tissues from high-A. muciniphila UC patients had a higher NLRP3 expression than that from low-A. muciniphila UC patients. Moreover, the upregulation of NLRP3 was observed in mouse macrophage Raw264.7 cells and bone marrow-derived macrophage (BMDM) cells after incubation with A. muciniphila. To clarify whether the protective effect of A. muciniphila in colitis depends on NLRP3, we performed the NLRP3-deficient assay in NLRP3−/− mice in vivo. The evidence showed that NLRP3 deficiency eliminated the protective effects of A. muciniphila in acute colitis. In conclusion, A. muciniphila alleviates DSS-induced acute colitis by NLRP3 activation, which enriches the mechanism and provides a new prospect for the probiotic-based treatment of colitis.IMPORTANCE The gut microbiota and host immune response interaction influences the progression of intestinal inflammatory disease. As a well-recognized next-generation probiotic, Akkermansia muciniphila has been proved to play a crucial role in the progression of colitis, but its underlying mechanism remains inconclusive. We found that oral administration of A. muciniphila strain BAA-835 significantly ameliorated the symptoms of acute colitis. Mechanistically, the expression of NLRP3 was upregulated in the A. muciniphila group, and the protective effect of A. muciniphila in colitis depends on NLRP3 activation. This enriches the mechanism and provides a new prospect for the probiotic-based treatment of colitis, which would promote a deeper understanding of the complex characteristics of A. muciniphila and provide guidance for the treatment of human colitis in the future.

Highlights

  • IMPORTANCE The gut microbiota and host immune response interaction influences the progression of intestinal inflammatory disease

  • We found the reduced levels of B. adolescentis, B. breve, B. longum, and A. muciniphila in the ulcerative colitis (UC) patients compared to the healthy people, but the levels of L. lactis and S. salivarius were increased in UC patients, while L. mucosae and F. prausnitzii had no difference (Fig. 1A to H)

  • To identify whether A. muciniphila influenced the inflammatory response in the colon tissue, we examined the mRNA level of tumor necrosis factor alpha (TNF-a), interleukin-6 (IL-6), and monocyte chemoattractant protein 1 (MCP-1) and we found a decreased trend in the A. muciniphila group colon tissues compared with the phosphate-buffered saline (PBS) group (Fig. 3E to G)

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Summary

Introduction

IMPORTANCE The gut microbiota and host immune response interaction influences the progression of intestinal inflammatory disease. The expression of NLRP3 was upregulated in the A. muciniphila group, and the protective effect of A. muciniphila in colitis depends on NLRP3 activation This enriches the mechanism and provides a new prospect for the probiotic-based treatment of colitis, which would promote a deeper understanding of the complex characteristics of A. muciniphila and provide guidance for the treatment of human colitis in the future. The purpose of this study is to confirm the effect of A. muciniphila on colitis, including the impact on symptom phenotype as well as its potential molecular mechanism It will promote a deeper understanding of the complex characteristics of A. muciniphila and provide guidance for the treatment of human colitis in the future

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