<i>Candida albicans</i> colonization modulates murine ethanol consumption and behavioral responses through elevation of serum prostaglandin E <sub>2</sub> and impact on the striatal dopamine system

<i>Candida albicans</i> is a commensal yeast that is found in the gut of most individuals. <i>C. albicans</i> has been shown to contribute to alcoholic liver disease. Outside of this, the impact of intestinal fungi on alcohol use disorder (AUD) had been unstudied. As AUD is a complex disorder characterized by high relapse rates and there are only three FDA-approved therapies for the maintenance of abstinence, it is important to study novel AUD contributors to find new therapeutic targets. Here, we show that an intestinal fungus, <i>C. albicans</i>, can alter mammalian ethanol consumption through an immune modulator, prostaglandin E<sub>2</sub>. The results highlight novel contributors to AUD-related phenotypes and further implicate the gut-brain axis in AUD. Future studies could lead to new therapeutic avenues for the treatment of AUD.

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Publication Details

Journal
mBio
Published
2025-10-16
DOI
https://doi.org/10.1128/mbio.02239-25
Primary Topic
Gut microbiota and health
Type
article
Field-Weighted Citation Impact
0.00
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article

Candida albicans colonization modulates murine ethanol consumption and behavioral responses through elevation of serum prostaglandin E 2 and impact on the striatal dopamine system

A. W. Day, Jamie Maguire, Alyssa DiLeo, Katrina Blandino et al.
mBio
Gut microbiota and health
article

Candida albicans colonization modulates murine ethanol consumption and behavioral responses through elevation of serum prostaglandin E 2 and impact on the striatal dopamine system

A. W. Day, Jamie Maguire, Alyssa DiLeo, Katrina Blandino, Carol A. Kumamoto, Emma Hayes, Jeyra Perez-Lozada
article en

Abstract

<i>Candida albicans</i> is a commensal yeast that is found in the gut of most individuals. <i>C. albicans</i> has been shown to contribute to alcoholic liver disease. Outside of this, the impact of intestinal fungi on alcohol use disorder (AUD) had been unstudied. As AUD is a complex disorder characterized by high relapse rates and there are only three FDA-approved therapies for the maintenance of abstinence, it is important to study novel AUD contributors to find new therapeutic targets. Here, we show that an intestinal fungus, <i>C. albicans</i>, can alter mammalian ethanol consumption through an immune modulator, prostaglandin E<sub>2</sub>. The results highlight novel contributors to AUD-related phenotypes and further implicate the gut-brain axis in AUD. Future studies could lead to new therapeutic avenues for the treatment of AUD.

mBioVol. 16(11)
Tufts University (US)
Openalex Percentile: Top 74%
Gut microbiota and health
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