Expression dynamics of secreted protease genes in Trichophyton rubrum induced by key host's proteinaceous components

Wenchuan Leng1, Tao Liu, Jin Wang

  • 1State Key Laboratory for Molecular Virology and Genetic Engineering, Institute of Pathogen Biology, Chinese Academy of Medical Sciences, Beijing, PR China.

Medical Mycology
|November 6, 2009
PubMed

Insights

Trichophyton rubrum secretes specific proteases during skin infections. Identifying these subtilisin (SUB) and metalloprotease (MEP) genes, like Sub3, Sub4, and Mep4, offers new antifungal treatment targets.

Area of Science:

  • Mycology
  • Molecular Biology
  • Dermatology

Background:

  • Trichophyton rubrum is a common cause of dermatophytosis, affecting millions globally.
  • The molecular mechanisms of T. rubrum pathogenicity, particularly secreted proteases, are not fully understood.
  • Secreted proteases are recognized as key virulence factors in T. rubrum infections.

Purpose of the Study:

  • To investigate the expression patterns and dynamics of secreted subtilisin (SUB) and metalloprotease (MEP) gene families in T. rubrum.
  • To identify specific protease genes involved in T. rubrum pathogenesis under simulated host infection conditions.

Main Methods:

  • Simulated host infection conditions were established.
  • Relative quantification using real-time PCR was employed to analyze gene expression.
  • Expression levels were assessed in response to keratin, collagen, elastin, and human skin sections.

Main Results:

  • Keratin, collagen, and elastin induced the expression of similar protease genes.
  • Protease gene expression patterns differed between individual protein substrates and human skin sections.
  • Sub3, Sub4, and Mep4 showed distinct expression dynamics, suggesting their dominance during infection.

Conclusions:

  • Sub3, Sub4, and Mep4 are likely the dominant secreted proteases during T. rubrum host infection.
  • These identified proteases represent potential targets for novel antifungal therapies.
  • The study provides molecular insights into dermatophytosis pathogenesis and suggests diagnostic markers.