Molecular ecology and pathogenic potential of Fonsecaea species

G S De Hoog1, D Attili-Angelis, V A Vicente

  • 1Centraalbureau voor Schimmelcultures, Utrecht, The Netherlands. de.hoog@cbs.knaw.nl

Medical Mycology
|November 24, 2004
PubMed

Insights

This study revises the Fonsecaea genus using ribosomal DNA internal transcribed spacer (ITS) sequencing, identifying two species: Fonsecaea pedrosoi and Fonsecaea monophora. Fonsecaea pedrosoi is strictly linked to chromoblastomycosis, while Fonsecaea monophora is a general opportunist.

Area of Science:

  • Medical Mycology
  • Molecular Systematics
  • Fungal Pathogenesis

Background:

  • The genus Fonsecaea comprises fungi implicated in human chromoblastomycosis.
  • Previous classifications relied on morphological characteristics, leading to ambiguity in species delineation.
  • Understanding the genetic diversity and pathogenic potential of Fonsecaea is crucial for disease management.

Purpose of the Study:

  • To revise the taxonomic classification of the genus Fonsecaea using molecular data.
  • To differentiate between Fonsecaea species and their etiological roles in chromoblastomycosis.
  • To investigate the genetic diversity within Fonsecaea strains.

Main Methods:

  • Ribosomal DNA internal transcribed spacer (ITS) sequencing was employed for phylogenetic analysis.
  • Randomly amplified polymorphic DNA (RAPD) typing was used for subspecific strain differentiation.
  • Morphological characterization was performed to assess species distinctions.

Main Results:

  • Two distinct species, Fonsecaea pedrosoi and the newly defined Fonsecaea monophora, were identified based on ITS sequence data.
  • The classical distinction of Fonsecaea pedrosoi and Fonsecaea compacta was found to be invalid, with F. compacta being a morphological variant.
  • Fonsecaea pedrosoi shows a strict association with human chromoblastomycosis, whereas F. monophora acts as a more general opportunist.
  • Subspecific RAPD typing revealed significant strain diversity within Fonsecaea, alongside evidence of clonal reproduction.
  • Fonsecaea-like environmental isolates were often more closely related to Cladophialophora species than to Fonsecaea.

Conclusions:

  • The molecular revision clarifies the taxonomy of the genus Fonsecaea, establishing F. pedrosoi and F. monophora as the key species.
  • Differential pathogenic roles in chromoblastomycosis are highlighted, with F. pedrosoi as a primary agent and F. monophora as an opportunist.
  • High genetic diversity exists within Fonsecaea, necessitating further investigation into strain-level variations and their clinical relevance.
  • Environmental isolates with Fonsecaea-like morphology may represent distinct taxa, potentially within the Cladophialophora genus, requiring careful identification in clinical settings.

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