Targeted gene disruption reveals an adhesin indispensable for pathogenicity of Blastomyces dermatitidis

J Exp Med. 1999 Apr 19;189(8):1207-16. doi: 10.1084/jem.189.8.1207.

Abstract

Systemic fungal infections are becoming more common and difficult to treat, yet the pathogenesis of these infectious diseases remains poorly understood. In many cases, pathogenicity can be attributed to the ability of the fungi to adhere to target tissues, but the lack of tractable genetic systems has limited progress in understanding and interfering with the offending fungal products. In Blastomyces dermatitidis, the agent of blastomycosis, a respiratory and disseminated mycosis of people and animals worldwide, expression of the putative adhesin encoded by the WI-1 gene was investigated as a possible virulence factor. DNA-mediated gene transfer was used to disrupt the WI-1 locus by allelic replacement, resulting in impaired binding and entry of yeasts into macrophages, loss of adherence to lung tissue, and abolishment of virulence in mice; each of these properties was fully restored after reconstitution of WI-1 by means of gene transfer. These findings establish the pivotal role of WI-1 in adherence and virulence of B. dermatitidis yeasts. To our knowledge, they offer the first example of a genetically proven virulence determinant among systemic dimorphic fungi, and underscore the value of reverse genetics for studies of pathogenesis in these organisms.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alleles
  • Animals
  • Blastomyces / genetics*
  • Blastomyces / pathogenicity
  • Blastomycosis / microbiology
  • Cell Adhesion Molecules / genetics
  • Fungal Proteins / genetics*
  • Gene Targeting / methods
  • Gene Transfer Techniques
  • Glycoproteins / genetics*
  • Lung / microbiology
  • Lung / pathology
  • Mice
  • Phenotype
  • Virulence

Substances

  • Cell Adhesion Molecules
  • Fungal Proteins
  • Glycoproteins