Heat Shock Proteins in Medically Relevant Fungal Pathogens: From Molecular Chaperones to Virulence Factors and Therapeutic Targets
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Updated: Jun 26, 2026

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Published on: July 21, 2021
Leonardo Padró-Villegas1, Héctor M Mora-Montes1
1Departamento de Biología, División de Ciencias Naturales y Exactas, Campus Guanajuato, Universidad de Guanajuato, Noria Alta s/n, col. Noria Alta, Guanajuato 36050, Gto., Mexico.
Abstract:
Heat shock proteins (HSPs) are highly conserved molecular chaperones that play a key role in maintaining protein homeostasis and cellular survival under stress conditions. Clinically relevant human pathogenic fungi include opportunistic fungi, dimorphic fungi, dermatophytes, Mucorales, and other pathogenic groups. HSPs, including Hsp90, Hsp70, Hsp60, Hsp40, and Hsp110, are essential for the correct nascent protein folding, aggregation prevention, and degradation of misfolded polypeptides. Fungal pathogens frequently encounter environmental and host-imposed stresses, including oxidative stress, temperature fluctuations, and antifungal treatments. This review synthesizes and critically analyzes current evidence on the role of HSP families in essential processes linked to fungal virulence, including morphogenetic transitions, biofilm formation, maintenance of cell wall integrity, and interactions with host immune cells. Beyond their canonical chaperone functions, HSPs act as central mediators in pathogenic processes, such as morphogenesis transitions, biofilm formation, cell wall integrity, and interactions with host immune cells. Hsp90 stabilizes key signaling proteins involved in stress responses, morphogenesis, and antifungal resistance, while Hsp60 and Hsp70 contribute to mitochondrial function, cell wall integrity, and immune modulation. Disruption of these chaperones impairs growth, reduces virulence, and increases susceptibility to antifungal agents. The rise of antifungal resistance underscores the urgent need for new therapeutic strategies. Targeting fungal HSPs has emerged as a promising approach due to their essential roles in stress tolerance and pathogenesis. Hsp90 inhibitors, including geldanamycin derivatives and other small molecules, have demonstrated the ability to impair fungal growth, reduce virulence traits, and sensitize resistant strains to conventional antifungal drugs. Combining HSP inhibitors with existing antifungal drugs represents a potential strategy to overcome resistance and improve treatment outcomes. This review summarizes the current knowledge on HSPs in pathogenic fungi, focusing on their roles in stress adaptation, virulence, host-pathogen interaction, antifungal resistance, and their potential as targets for novel antifungal therapies.
Insights
Heat shock proteins (HSPs) are crucial for fungal survival and virulence. Targeting these essential fungal proteins offers a promising strategy to combat drug-resistant infections and improve antifungal therapies.
Area of Science:
- Molecular Biology
- Mycology
- Immunology
Background:
- Heat shock proteins (HSPs) are vital molecular chaperones maintaining protein homeostasis and cellular survival under stress.
- Clinically significant pathogenic fungi face various stresses, including host-imposed immune responses and antifungal treatments.
- HSPs are essential for fungal growth, protein folding, and preventing polypeptide aggregation.
Purpose of the Study:
- To review and analyze the role of HSP families in fungal virulence.
- To explore HSPs' involvement in morphogenesis, biofilm formation, cell wall integrity, and host immune interactions.
- To assess the potential of targeting fungal HSPs as a novel antifungal therapeutic strategy.
Main Methods:
- Literature review and critical analysis of current evidence on HSPs in pathogenic fungi.
- Synthesis of data on HSP functions in fungal stress adaptation and virulence.
- Examination of studies investigating HSP inhibitors for antifungal drug development.
Main Results:
- HSPs are central mediators of fungal pathogenesis, influencing morphogenesis, biofilm formation, and immune cell interactions.
- Hsp90, Hsp70, and Hsp60 play critical roles in stress response, mitochondrial function, and cell wall integrity.
- Disruption of HSPs impairs fungal growth, reduces virulence, and increases susceptibility to antifungals.
Conclusions:
- Fungal HSPs are essential for stress tolerance, virulence, and antifungal resistance.
- Targeting HSPs, particularly with inhibitors like geldanamycin derivatives, shows promise for overcoming antifungal resistance.
- Combining HSP inhibitors with conventional antifungals may improve treatment outcomes for fungal infections.
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