Candidalysin biology and activation of host cells

Author:

Lortal Léa1ORCID,Lyon Claire M.1,Sprague Jakob L.2,Sonnberger Johannes2,Paulin Olivia K. A.1,Wickramasinghe Don N.1,Richardson Jonathan P.1ORCID,Hube Bernhard234ORCID,Naglik Julian R.1ORCID

Affiliation:

1. Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral and Craniofacial Sciences, King’s College London

2. Department of Microbial Pathogenicity Mechanisms, Leibniz Institute for Natural Product Research and Infection Biology–Hans Knöll Institute (HKI)

3. Institute of Microbiology, Friedrich Schiller University

4. Cluster of Excellence Balance of the Microverse, Friedrich Schiller University Jena

Abstract

ABSTRACT Candida albicans is an opportunistic fungal pathogen that can cause life-threatening systemic infections and distressing mucosal infections. A major breakthrough in understanding C. albicans pathogenicity was the discovery of candidalysin, the first cytolytic peptide toxin identified in a human pathogenic fungus. Secreted by C. albicans hyphae and encoded by the ECE1 gene, this 31-amino acid peptide integrates into and permeabilizes host cell membranes, causing damage across diverse cell types. Beyond its cytolytic activity, candidalysin can trigger potent innate immune responses in epithelial cells, macrophages, and neutrophils. Additionally, candidalysin plays a key role in nutrient acquisition during infection. This review explores the biology of candidalysin, its role in host cell activation, and extends the discussion to non-candidalysin Ece1p peptides, shedding light on their emerging significance.

Funder

Wellcome Trust

National Institutes of Health

Deutsche Forschungsgemeinschaft

Bundesministerium für Bildung und Forschung

Publisher

American Society for Microbiology

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