# Comprehensive Insights into Sugar Transporters of Candidozyma auris and Their Roles in Antifungal Resistance

**Authors:** Praveen Kumar, Mohit Kumar, Amandeep Saini, Sheikh Owais Mohamad, Basharat Ali, Brooke D. Esquivel, Atanu Banerjee, Theodore C. White, Naseem A. Gaur, Abdul Haseeb Shah, Amresh Prakash, Rajendra Prasad

PMC · DOI: 10.3390/jof12020094 · 2026-01-30

## TL;DR

This study explores how sugar transporters in Candidozyma auris may contribute to antifungal resistance by affecting drug import and membrane permeability.

## Contribution

The study identifies Hgt13p as a key sugar transporter involved in fluconazole import and resistance in Candidozyma auris.

## Key findings

- C. auris HGTs are more closely related to C. albicans than S. cerevisiae.
- The Δhgt13 strain shows increased fluconazole resistance and reduced intracellular drug accumulation.
- Molecular simulations confirm strong interactions between fluconazole and Hgt13p.

## Abstract

In Candida species, including Candidozyma auris (formerly Candida auris), overexpression of efflux pumps is a well-established mechanism of antifungal resistance. However, accumulating evidence indicates that impaired drug import may also significantly contribute to reduced antifungal susceptibility. Sugar importers, historically viewed solely as hexose transporters (HGTs), are now emerging as potential indirect modulators of antifungal uptake. Here, we performed a comprehensive inventory and functional analysis of the HGT family in C. auris to assess its contribution to antifungal import. Phylogenetic analyses revealed that C. auris HGTs are more closely related to those of Candida albicans (C. albicans) than Saccharomyces cerevisiae (S. cerevisiae). All HGT genes showed basal expression, with several significantly downregulated upon fluconazole (FLC) exposure. To establish functional relevance, we generated a mini-library of HGT deletion mutants. Notably, the Δhgt13 strain exhibited markedly increased FLC resistance, concomitant with reduced intracellular FLC accumulation and decreased membrane permeability. Consistently, molecular docking and molecular dynamics simulations demonstrated strong and stable interactions between FLC and Hgt13p. Together, these findings implicate Hgt13p as a key determinant of FLC import and membrane permeability, revealing reduced FLC import could also contribute to antifungal resistance in C. auris.

## Linked entities

- **Genes:** LOC114118004 (keratin-associated protein 8-1) [NCBI Gene 114118004], HGT13 (Hgt13p) [NCBI Gene 2913462]
- **Chemicals:** fluconazole (PubChem CID 3365)
- **Species:** Candidozyma auris (taxon 498019), Candida albicans (taxon 5476), Saccharomyces cerevisiae (taxon 4932)

## Full-text entities

- **Diseases:** fungal (MESH:D009181), HIV/AIDS (MESH:D015658), invasive (MESH:D009361), infections (MESH:D007239), injury to (MESH:D014947)
- **Chemicals:** hydrogen (MESH:D006859), cycloheximide (MESH:D003513), echinocandin (MESH:D054714), SDS (MESH:D012967), DMSO (MESH:D004121), ethanol (MESH:D000431), D-glucose (MESH:D005947), FLC (MESH:D015725), phospholipids (MESH:D010743), phenol (MESH:D019800), ATP (MESH:D000255), water (MESH:D014867), polyenes (MESH:D011090), disaccharides (MESH:D004187), lipid (MESH:D008055), 4-NQO (MESH:D015112), chloroform (MESH:D002725), sterol (MESH:D013261), nourseothricin (MESH:D013309), TES (MESH:C004551), sulfometuron methyl (MESH:C042031), AMB (MESH:D000666), flucytosine (MESH:D005437), miltefosine (MESH:C039128), POPC (MESH:C065191), EDTA (MESH:D004492), monosaccharides (MESH:D009005), Cl- (MESH:D002713), (dT (MESH:D013936), N-phenyl-1-naphthylamine (MESH:C005444), Azole (MESH:D001393), carbohydrate (MESH:D002241), carbon (MESH:D002244), lithium acetate (MESH:C488804), PEG (-), saline (MESH:D012965), 3H (MESH:D014316), proton (MESH:D011522), Sugar (MESH:D000073893), DEPC (MESH:D004047), Na+ (MESH:D012964)
- **Species:** Cryptococcus neoformans (Cryptococcus neoformans serotype A, species) [taxon 5207], Nakaseomyces glabratus (species) [taxon 5478], Candidozyma auris (species) [taxon 498019], Homo sapiens (human, species) [taxon 9606], Candida [taxon 1535326], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Aspergillus fumigatus (species) [taxon 746128], Candida albicans (species) [taxon 5476], Escherichia coli (E. coli, species) [taxon 562], Petrachloros mirabilis (species) [taxon 2918835]
- **Mutations:** 80  C, C at 200, Met80Gly, C for 24-48
- **Cell lines:** CBS10913T — Homo sapiens (Human), Transformed cell line (CVCL_AK31)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942029/full.md

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Source: https://tomesphere.com/paper/PMC12942029