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Candidalysin is a fungal peptide toxin critical for mucosal infection.
Moyes, David L; Wilson, Duncan; Richardson, Jonathan P; Mogavero, Selene; Tang, Shirley X; Wernecke, Julia; Höfs, Sarah; Gratacap, Remi L; Robbins, Jon; Runglall, Manohursingh; Murciano, Celia; Blagojevic, Mariana; Thavaraj, Selvam; Förster, Toni M; Hebecker, Betty; Kasper, Lydia; Vizcay, Gema; Iancu, Simona I; Kichik, Nessim; Häder, Antje; Kurzai, Oliver; Luo, Ting; Krüger, Thomas; Kniemeyer, Olaf; Cota, Ernesto; Bader, Oliver; Wheeler, Robert T; Gutsmann, Thomas; Hube, Bernhard; Naglik, Julian R.
Afiliación
  • Moyes DL; Mucosal &Salivary Biology Division, Dental Institute, King's College London SE1 1UL, UK.
  • Wilson D; Department of Microbial Pathogenicity Mechanisms, Hans Knöll Institute, D-07745 Jena, Germany.
  • Richardson JP; Mucosal &Salivary Biology Division, Dental Institute, King's College London SE1 1UL, UK.
  • Mogavero S; Department of Microbial Pathogenicity Mechanisms, Hans Knöll Institute, D-07745 Jena, Germany.
  • Tang SX; Mucosal &Salivary Biology Division, Dental Institute, King's College London SE1 1UL, UK.
  • Wernecke J; Research Center Borstel, Division of Biophysics, D-23845 Borstel, Germany.
  • Höfs S; Deutsches Elektronen-Synchrotron DESY, D-22607 Hamburg, Germany.
  • Gratacap RL; Department of Microbial Pathogenicity Mechanisms, Hans Knöll Institute, D-07745 Jena, Germany.
  • Robbins J; Department of Molecular &Biomedical Sciences, University of Maine, Orono, Maine 04469, USA.
  • Runglall M; Wolfson CARD, King's College London, Guy's Campus, London SE1 1UL, UK.
  • Murciano C; Mucosal &Salivary Biology Division, Dental Institute, King's College London SE1 1UL, UK.
  • Blagojevic M; Mucosal &Salivary Biology Division, Dental Institute, King's College London SE1 1UL, UK.
  • Thavaraj S; Mucosal &Salivary Biology Division, Dental Institute, King's College London SE1 1UL, UK.
  • Förster TM; Mucosal &Salivary Biology Division, Dental Institute, King's College London SE1 1UL, UK.
  • Hebecker B; Department of Microbial Pathogenicity Mechanisms, Hans Knöll Institute, D-07745 Jena, Germany.
  • Kasper L; Department of Microbial Pathogenicity Mechanisms, Hans Knöll Institute, D-07745 Jena, Germany.
  • Vizcay G; Research Group Microbial Immunology, Hans Knöll Institute, D-07745 Jena, Germany.
  • Iancu SI; Department of Microbial Pathogenicity Mechanisms, Hans Knöll Institute, D-07745 Jena, Germany.
  • Kichik N; Centre for Ultrastructural Imaging, King's College London, London SE1 1UL, UK.
  • Häder A; Mucosal &Salivary Biology Division, Dental Institute, King's College London SE1 1UL, UK.
  • Kurzai O; Mucosal &Salivary Biology Division, Dental Institute, King's College London SE1 1UL, UK.
  • Luo T; Department of Life Sciences, Imperial College London, London SW7 2AZ, UK.
  • Krüger T; Septomics Research Center, Hans-Knöll Institute and Friedrich Schiller University, D-07745 Jena, Germany.
  • Kniemeyer O; Septomics Research Center, Hans-Knöll Institute and Friedrich Schiller University, D-07745 Jena, Germany.
  • Cota E; Department of Molecular and Applied Microbiology, Hans Knöll Institute, D-07745 Jena, Germany.
  • Bader O; Department of Molecular and Applied Microbiology, Hans Knöll Institute, D-07745 Jena, Germany.
  • Wheeler RT; Department of Molecular and Applied Microbiology, Hans Knöll Institute, D-07745 Jena, Germany.
  • Gutsmann T; Department of Life Sciences, Imperial College London, London SW7 2AZ, UK.
  • Hube B; Institute for Medical Microbiology, University Medical Center Göttingen, D-37075 Göttingen, Germany.
  • Naglik JR; Department of Molecular &Biomedical Sciences, University of Maine, Orono, Maine 04469, USA.
Nature ; 532(7597): 64-8, 2016 Apr 07.
Article en En | MEDLINE | ID: mdl-27027296
ABSTRACT
Cytolytic proteins and peptide toxins are classical virulence factors of several bacterial pathogens which disrupt epithelial barrier function, damage cells and activate or modulate host immune responses. Such toxins have not been identified previously in human pathogenic fungi. Here we identify the first, to our knowledge, fungal cytolytic peptide toxin in the opportunistic pathogen Candida albicans. This secreted toxin directly damages epithelial membranes, triggers a danger response signalling pathway and activates epithelial immunity. Membrane permeabilization is enhanced by a positive charge at the carboxy terminus of the peptide, which triggers an inward current concomitant with calcium influx. C. albicans strains lacking this toxin do not activate or damage epithelial cells and are avirulent in animal models of mucosal infection. We propose the name 'Candidalysin' for this cytolytic peptide toxin; a newly identified, critical molecular determinant of epithelial damage and host recognition of the clinically important fungus, C. albicans.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Asunto principal: Candida albicans / Proteínas Fúngicas / Citotoxinas / Factores de Virulencia / Micotoxinas Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Nature Año: 2016 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Asunto principal: Candida albicans / Proteínas Fúngicas / Citotoxinas / Factores de Virulencia / Micotoxinas Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Nature Año: 2016 Tipo del documento: Article País de afiliación: Reino Unido