KOR

e-Article

The RodA Hydrophobin on Aspergillus fumigatus Spores Masks Dectin-1– and Dectin-2–Dependent Responses and Enhances Fungal Survival In Vivo
Document Type
article
Source
The Journal of Immunology. 191(5)
Subject
Biological Sciences
Biomedical and Clinical Sciences
Microbiology
Clinical Sciences
Medical Microbiology
Biodefense
Emerging Infectious Diseases
Prevention
Infectious Diseases
Vaccine Related
Aetiology
2.2 Factors relating to the physical environment
Infection
Animals
Aspergillosis
Aspergillus fumigatus
Corneal Diseases
Disease Models
Animal
Fungal Proteins
Immunohistochemistry
Lectins
C-Type
Mice
Mice
Inbred C57BL
Spores
Fungal
Virulence
Virulence Factors
Immunology
Biochemistry and cell biology
Language
Abstract
Aspergillus and Fusarium species are important causes of fungal infections worldwide. Airborne spores (conidia) of these filamentous fungi express a surface protein that confers hydrophobicity (hydrophobin) and covers cell wall components that would otherwise induce a host immune cell response. Using a mutant Aspergillus fumigatus strain (ΔrodA) that does not express the RodA hydrophobin, and Aspergillus and Fusarium conidia from clinical isolates that were treated with hydrofluoric acid (which removes the A. fumigatus RodA protein), we observed increased surface exposure of β1,3-glucan and α-mannose on Aspergillus and Fusarium conidia. We also found that ΔrodA and hydrofluoric acid-treated conidia stimulate significantly higher NF-κB p65 nuclear translocation and cytokine production by macrophages from C57BL/6, but not from Dectin-1(-/-) or Dectin-2(-/-) mice. Using a murine model of A. fumigatus corneal infection, we showed that ΔrodA conidia induced significantly higher cytokine production, neutrophil infiltration, and more rapid fungal clearance from C57BL/6 corneas compared with the parent G10 strain, which was dependent on Dectin-1 and Dectin-2. Together, these findings identify the hydrophobin RodA as a virulence factor that masks Dectin-1 and Dectin-2 recognition of conidia, resulting in impaired neutrophil recruitment to the cornea and increased fungal survival and clinical disease.