# Genomic Analysis Reveals Diversified and Stress-Responsive Transport Repertoire in Candidozyma (Candida) auris

**Authors:** Raymond Cai, Jianying Gu

PMC · DOI: 10.3390/jof12030174 · Journal of Fungi · 2026-02-28

## TL;DR

This study identifies a diverse set of transporters in the dangerous fungus C. auris, which may help it survive stress and resist antifungal drugs.

## Contribution

The first comprehensive characterization of transporters in C. auris, revealing their diversity and stress-responsive roles.

## Key findings

- C. auris has 686 transporters and 125 accessory factors, most previously uncharacterized.
- Transporter families show lineage-specific divergence compared to other Candida species.
- Certain transporters are transcriptionally active under antifungal stress conditions.

## Abstract

Candidozyma (Candida) auris is a fungal pathogen associated with life-threatening invasive infections and high mortality rates. It is becoming a major global public health concern due to its ability to resist multiple antifungal drugs and spread in healthcare settings. Despite this, little is known about the mechanisms underlying drug resistance, fungal development, pathogenesis, and virulence. Among the factors contributing to these processes, transporters play a central role in fungal biology, regulating nutrient acquisition, metabolite exchange, ion homeostasis, and drug efflux. However, the composition and diversity of transporter systems in C. auris remain poorly defined. Through genomic analysis, we identified 686 transporters and 125 accessory factors involved in transport in C. auris, most of which had not been characterized. These transporters and accessory factors were classified into seven classes, 22 subclasses, and 215 families, reflecting substantial functional diversity. Comparative analyses with other pathogenic Candida species and Saccharomyces cerevisiae reveal lineage-specific divergence in several transporter families. We also integrated multiple publicly available RNA-seq datasets encompassing antifungal drug exposure and drug-resistant isolates and identified subsets of transporters that are transcriptionally responsive in distinct antifungal conditions, including members of families implicated in drug transport, metabolism, and ion homeostasis. Together, this study defines the landscape of transporter systems in C. auris and highlights transporter families that may contribute to stress adaptation and antifungal responses, providing a resource for future functional and mechanistic investigations.

## Linked entities

- **Species:** Saccharomyces cerevisiae (taxon 4932)

## Full-text entities

- **Diseases:** injury to (MESH:D014947), infections (MESH:D007239), MFS (MESH:D004830), fungal (MESH:D009181), C. auris infections (MESH:C000656864), MDR (MESH:D018088), COVID-19 (MESH:D000086382)
- **Chemicals:** AZR1 (-), ROS (MESH:D017382), phosphate (MESH:D010710), azole (MESH:D001393), manganese (MESH:D008345), arsenite (MESH:C015001), amino acid (MESH:D000596), glutathione (MESH:D005978), ergosterol (MESH:D004875), polyamine (MESH:D011073), fatty acid (MESH:D005227), carbon (MESH:D002244), Echinocandin (MESH:D054714), ATP (MESH:D000255), metal (MESH:D008670), arsenic (MESH:D001151), tetracycline (MESH:D013752), Polyene (MESH:D011090), Iron (MESH:D007501), triazole (MESH:D014230), Fluconazole (MESH:D015725), hexose (MESH:D006601), Caspofungin (MESH:D000077336), nitrogen (MESH:D009584), glucose (MESH:D005947), lipid (MESH:D008055), oligomycin (MESH:D009840), nucleotide (MESH:D009711), quinidine (MESH:D011802), copper (MESH:D003300), AmB (MESH:D000666), zinc (MESH:D015032), Sugar (MESH:D000073893)
- **Species:** Histoplasma capsulatum (species) [taxon 5037], Fusarium graminearum (species) [taxon 5518], Petrachloros mirabilis (species) [taxon 2918835], Candidozyma auris (species) [taxon 498019], Penicillium digitatum (species) [taxon 36651], Candida maltosa (species) [taxon 5479], Coccidioides immitis (species) [taxon 5501], Aspergillus fumigatus (species) [taxon 746128], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Lodderomyces parapsilosis (species) [taxon 5480], Nakaseomyces glabratus (species) [taxon 5478], Alternaria alternata (species) [taxon 5599], Homo sapiens (human, species) [taxon 9606], Candida dubliniensis CD36 (strain) [taxon 573826], Cryptococcus neoformans (Cryptococcus neoformans serotype A, species) [taxon 5207], Candida albicans SC5314 (strain) [taxon 237561], Candida dubliniensis (species) [taxon 42374], Candida albicans (species) [taxon 5476]
- **Mutations:** TAC1A, R467K
- **Cell lines:** S288C. — Homo sapiens (Human), Finite cell line (CVCL_L938), CBS 10913T. — Homo sapiens (Human), Transformed cell line (CVCL_AK31), B8441 — Homo sapiens (Human), Transformed cell line (CVCL_5C15)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13028451/full.md

## References

167 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028451/full.md

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Source: https://tomesphere.com/paper/PMC13028451