Nutrients (Aug 2024)

Effect of Mutant and Engineered High-Acetate-Producing <i>Saccharomyces cerevisiae</i> var. <i>boulardii</i> Strains in Dextran Sodium Sulphate-Induced Colitis

  • Sara Deleu,
  • Inge Jacobs,
  • Jorge F. Vazquez Castellanos,
  • Sare Verstockt,
  • Bruna Trindade de Carvalho,
  • Ana Subotić,
  • Bram Verstockt,
  • Kaline Arnauts,
  • Lowie Deprez,
  • Eva Vissers,
  • Matthias Lenfant,
  • Greet Vandermeulen,
  • Gert De Hertogh,
  • Kristin Verbeke,
  • Gianluca Matteoli,
  • Geert R. B. Huys,
  • Johan M. Thevelein,
  • Jeroen Raes,
  • Séverine Vermeire

DOI
https://doi.org/10.3390/nu16162668
Journal volume & issue
Vol. 16, no. 16
p. 2668

Abstract

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Acetate-producing Saccharomyces cerevisiae var. boulardii strains could exert improved effects on ulcerative colitis, which here, was preclinically evaluated in an acute dextran sodium sulphate induced model of colitis. Nine-week-old female mice were divided into 12 groups, receiving either drinking water or 2.75% dextran sodium sulphate for 7 days, combined with a daily gavage of various treatments with different levels of acetate accumulation: sham control (phosphate buffered saline, no acetate), non-probiotic control (Baker’s yeast, no acetate), probiotic control (Enterol®, transient acetate), and additionally several Saccharomyces cerevisiae var. boulardii strains with respectively no, high, and extra-high acetate accumulation. Disease activity was monitored daily, and feces samples were collected at different timepoints. On day 14, the mice were sacrificed, upon which blood and colonic tissue were collected for analysis. Disease activity in inflamed mice was lower when treated with the high-acetate-producing strain compared to sham and non-probiotic controls. The non-acetate-producing strain showed higher disease activity compared to the acetate-producing strains. Accordingly, higher histologic inflammation was observed in non- or transient-acetate-producing strains compared to the sham control, whereas this increase was not observed for high- and extra-high-acetate-producing strains upon induction of inflammation. These anti-inflammatory findings were confirmed by transcriptomic analysis of differentially expressed genes. Moreover, only the strain with the highest acetate production was superior in maintaining a stable gut microbial alpha-diversity upon inflammation. These findings support new possibilities for acetate-mediated management of inflammation in inflammatory bowel disease by administrating high-acetate-producing Saccharomyces cerevisae var. boulardii strains.

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