Fungal infection drives metabolic reprogramming in epithelial cells via aerobic glycolysis and an alternative TCA cycle shunt
- Aize Pellon
- Shervin Dokht Sadeghi Nasab
- Gholamreza Bidkhori
- James S. Griffiths
- Stefania Vaga
- Neelu Begum
- Mariana Blagojevic
- Nitesh Kumar Sigh
- Natalia K. Kotowicz
- Ifeanyi Uzochukwu
- Adrien Le Guennec
- Rhonda Henley-Smith
- Harry Gregson-Williams
- Frederick Clasen
- Miranda Pryce
- Nadia Karimpour
- Richard Cook
- Juan Anguita
- Jonathan P. Richardson
- Selvam Thavaraj
- Julian R. Naglik
- Saeed Shoaie
- David L. Moyes
2026-02-04
Candida albicans –induced immunometabolic changes drive complex responses in immune cells. However, whether and how C. albicans causes remodeling of oral epithelial cell (OEC) metabolism is unclear. Here, we use in vitro experiments and patient biopsies to demonstrate that OECs undergo metabolic reprogramming when infected by C. albicans independently of candidalysin secretion, increasing glycolysis and decreasing tricarboxylic acid (TCA) cycle activity. Glycolysis and glucose transport inhibition show that these pathways support OEC cytokine release, highlighting the partial control of antifungal epithelial immunity by cellular metabolism. However, glucose supplementation disrupts OEC responses both in vitro and in vivo, suggesting that the fungus benefits from these metabolic shifts and that increased aerobic glycolysis in OECs is detrimental. Genome-scale metabolic modeling predicted a shutdown of the TCA cycle and a previously unidentified role for glutamic-oxaloacetic transaminase 1 (GOT1) in response to C. albicans , which was subsequently shown to be important for OEC survival during infection. This study reveals a fundamental role for hexose metabolism and identifies a GOT1-mediated TCA cycle shunt in regulating OEC survival and immune responses during mucosal fungal infections.