Akkermansia muciniphila in the small intestine improves liver fibrosis in a murine liver cirrhosis model

NPJ Biofilms Microbiomes. 2024 Sep 16;10(1):81. doi: 10.1038/s41522-024-00564-y.

Abstract

Recent evidence indicates that liver cirrhosis (LC) is a reversible condition, but there is no established intervention against liver fibrosis. Although the gut microbiota is considered involved in the pathogenesis of LC, the underlying mechanisms remain unclear. Although the antibiotic, rifaximin (RFX), is effective for hepatic encephalopathy (HE) with LC, the impact of RFX on intestinal bacteria is unknown. We investigated the bacterial compositions along the GI tract under RFX treatment using a murine LC model. RFX improved liver fibrosis and hyperammonemia and altered the bacterial composition in the small intestine. The efficacy of RFX was associated with increases in specific bacterial genera, including Akkermansia. Administration of a commensal strain of Akkermansia muciniphila improved liver fibrosis and hyperammonemia with changing bacterial composition in the small intestine. This study proposed a new concept "small intestine-liver axis" in the pathophysiology of LC and oral A. muciniphila administration is a promising microbial intervention.

MeSH terms

  • Akkermansia*
  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Anti-Bacterial Agents / therapeutic use
  • Disease Models, Animal*
  • Gastrointestinal Microbiome* / drug effects
  • Intestine, Small* / microbiology
  • Intestine, Small* / pathology
  • Liver / microbiology
  • Liver / pathology
  • Liver Cirrhosis* / microbiology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • RNA, Ribosomal, 16S / genetics
  • Rifaximin* / pharmacology
  • Rifaximin* / therapeutic use
  • Verrucomicrobia

Substances

  • Rifaximin
  • Anti-Bacterial Agents
  • RNA, Ribosomal, 16S

Supplementary concepts

  • Akkermansia muciniphila