Proteome Analysis Reveals the Conidial Surface Protein CcpA Essential for Virulence of the Pathogenic Fungus Aspergillus fumigatus

Author:

Voltersen Vera12,Blango Matthew G.1ORCID,Herrmann Sahra3,Schmidt Franziska1,Heinekamp Thorsten12,Strassburger Maria4,Krüger Thomas1,Bacher Petra56,Lother Jasmin7,Weiss Esther7,Hünniger Kerstin89,Liu Hong1011,Hortschansky Peter12,Scheffold Alexander6,Löffler Jürgen7ORCID,Krappmann Sven12,Nietzsche Sandor13,Kurzai Oliver89,Einsele Hermann14,Kniemeyer Olaf12ORCID,Filler Scott G.1011,Reichard Utz3,Brakhage Axel A.12ORCID

Affiliation:

1. Department of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology (HKI), Jena, Germany

2. Department of Microbiology and Molecular Biology, Institute of Microbiology, Friedrich Schiller University Jena, Jena, Germany

3. Institute for Medical Microbiology, University Medical Center, Göttingen, Germany

4. Transfer Group Anti-infectives, Leibniz Institute for Natural Product Research and Infection Biology (HKI), Jena, Germany

5. Institute of Clinical Molecular Biology, Christian-Albrechts University Kiel, Kiel, Germany

6. Institute of Immunology, Christian-Albrechts University Kiel & Universitätsklinik Schleswig-Holstein, Kiel, Germany

7. Medical Clinic and Policlinic II, University Clinic Würzburg, Würzburg, Germany

8. Institute for Hygiene and Microbiology, University of Würzburg, Würzburg, Germany

9. Septomics Research Center, Leibniz Institute for Natural Product Research and Infection Biology (HKI), Jena, Germany

10. Division of Infectious Diseases, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California, USA

11. David Geffen School of Medicine at University of California, Los Angeles, Los Angeles, California, USA

12. Microbiology Institute-Clinical Microbiology, Immunology and Hygiene, University Hospital Erlangen and Friedrich-Alexander University of Erlangen-Nürnberg, Erlangen, Germany

13. Center for Electron Microscopy, Jena University Hospital, Jena, Germany

14. Internal Medicine II, University Hospital Würzburg, Würzburg, Germany

Abstract

The mammalian immune system relies on recognition of pathogen surface antigens for targeting and clearance. In the absence of immune evasion strategies, pathogen clearance is rapid. In the case of Aspergillus fumigatus , the successful fungus must avoid phagocytosis in the lung to establish invasive infection. In healthy individuals, fungal spores are cleared by immune cells; however, in immunocompromised patients, clearance mechanisms are impaired. Here, using proteome analyses, we identified CcpA as an important fungal spore protein involved in pathogenesis. A. fumigatus lacking CcpA was more susceptible to immune recognition and prompt eradication and, consequently, exhibited drastically attenuated virulence. In infection studies, CcpA was required for virulence in infected immunocompromised mice, suggesting that it could be used as a possible immunotherapeutic or diagnostic target in the future. In summary, our report adds a protein to the list of those known to be critical to the complex fungal spore surface environment and, more importantly, identifies a protein important for conidial immunogenicity during infection.

Funder

HHS | National Institutes of Health

Deutsche Forschungsgemeinschaft

Leibniz-Gemeinschaft

Bundesministerium für Bildung und Forschung

BMBF

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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