A member of the gut mycobiota modulates host purine metabolism exacerbating colitis in mice.

Abstract

The commensal microbiota has an important impact on host health, which is only beginning to be elucidated. Despite the presence of fungal, archaeal, and viral members, most studies have focused solely on the bacterial microbiota. Antibodies against the yeast <i>Saccharomyces cerevisiae</i> are found in some patients with Crohn's disease (CD), suggesting that the mycobiota may contribute to disease severity. We report that <i>S. cerevisiae</i> exacerbated intestinal disease in a mouse model of colitis and increased gut barrier permeability. Transcriptome analysis of colon tissue from germ-free mice inoculated with <i>S. cerevisiae</i> or another fungus, <i>Rhodotorula aurantiaca</i>, revealed that <i>S. cerevisiae</i> colonization affected the intestinal barrier and host metabolism. A fecal metabolomics screen of germ-free animals demonstrated that <i>S. cerevisiae</i> colonization enhanced host purine metabolism, leading to an increase in uric acid production. Treatment with uric acid alone worsened disease and increased gut permeability. Allopurinol, a clinical drug used to reduce uric acid, ameliorated colitis induced by <i>S. cerevisiae</i> in mice. In addition, we found a positive correlation between elevated uric acid and anti-yeast antibodies in human sera. Thus, yeast in the gut may be able to potentiate metabolite production that negatively affects the course of inflammatory bowel disease.