# p24 family proteins are critical for cell wall integrity, protein secretion, and virulence in Candida albicans

**Authors:** Xiangtai Yu, Hao Cui, Yifei Liu, Jian Yin, Jingkai Zhang, Gang Luo, Yang Lu, Chang Su

PMC · DOI: 10.1128/msphere.00827-25 · mSphere · 2026-01-20

## TL;DR

This study shows that p24 family proteins are essential for the cell wall, secretion of virulence factors, and survival of the fungal pathogen Candida albicans.

## Contribution

The study reveals the critical role of p24 proteins in C. albicans pathogenicity, particularly in cell wall integrity and virulence factor secretion.

## Key findings

- All four p24 family members are upregulated during invasive candidiasis and are required for cell wall integrity.
- p24 mutants show reduced virulence in a mouse model and decreased survival in macrophages.
- Defective secretion of virulence factors and lipases is observed in the absence of p24 proteins.

## Abstract

Candida albicans is a fungal commensal and also a prevalent pathogen of humans. p24 proteins are a family of type I membrane proteins regarded as cargo receptors for endoplasmic reticulum (ER) to Golgi transport and are thought to be involved in regulating secretion. Here, we sought to explore the impact of this family of proteins on C. albicans pathogenicity. The expression of all four members of the p24 family is upregulated during invasive candidiasis. Their expression is independent of yeast-to-hypha transition but is highly induced by tissue culture conditions. We then generated single deletion mutants for each member of the p24 family for phenotypic characterization. All these mutants exhibit significantly attenuated virulence in a mouse model of systemic infection and reduced survival in macrophages but are dispensable for vegetative growth and morphogenesis. They also show lower abundance of chitin and phosphomannan in the cell wall and enhanced sensitivity to fluconazole, an azole antifungal drug. Importantly, the absence of p24 proteins leads to defective protein secretion in C. albicans, including pathogenicity-related effectors and lipases, and reduces commensal fitness. These results suggest that p24 proteins are critical for cell wall integrity, secretion of virulence factors, and virulence in C. albicans.

Candida albicans is an important opportunistic fungal pathogen of immunocompromised individuals and a top-ranking WHO fungal priority pathogen due to the high frequency and mortality of invasive candidiasis. The eukaryotic p24 family of proteins has long been known to be key regulators of protein trafficking along the secretory pathway, but their potential roles regarding pathogenesis in C. albicans remain unknown. Here, we discover that all members of the p24 family are required for cell wall integrity, proper secretion of virulence factors, survival in macrophages, and virulence in a systemic infection model. However, they are dispensable for vegetative growth and yeast-to-hypha transition, the best-known virulence attribute. Our study systematically investigates C. albicans p24 proteins and highlights the critical role that the early secretory pathway plays in fungal pathogenicity.

## Linked entities

- **Chemicals:** fluconazole (PubChem CID 3365)
- **Diseases:** candidiasis (MONDO:0002026)
- **Species:** Candida albicans (taxon 5476)

## Full-text entities

- **Diseases:** fungal (MESH:D009181), invasive candidiasis (MESH:D058365), infection (MESH:D007239)
- **Chemicals:** fluconazole (MESH:D015725), phosphomannan (MESH:C005437), chitin (MESH:D002686)
- **Species:** Homo sapiens (human, species) [taxon 9606], Candida albicans (species) [taxon 5476], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Mus musculus (house mouse, species) [taxon 10090]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12931272/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12931272/full.md

## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12931272/full.md

---
Source: https://tomesphere.com/paper/PMC12931272