Molecular Characterization and Antifungal Susceptibility of Clinical Fusarium Species From Brazil

Patricia F Herkert1,2,3, Abdullah M S Al-Hatmi3,4,5, Gabriel L de Oliveira Salvador6

  • 1Instituto Carlos Chagas, Fundação Oswaldo Cruz, Curitiba, Brazil.

Insights

This study analyzed antifungal susceptibility in clinical Fusarium isolates, finding Amphotericin B effective against most strains. Fusarium keratoplasticum demonstrated resistance to several azole antifungals, highlighting treatment challenges.

Area of Science:

  • Medical Mycology
  • Antimicrobial Resistance
  • Clinical Microbiology

Background:

  • Fusarium species are environmental fungi causing human infections (fusariosis).
  • Several Fusarium species complexes are implicated in human diseases.
  • Accurate species identification is crucial for understanding fusariosis epidemiology and treatment.

Purpose of the Study:

  • To determine the antifungal susceptibility of clinical Fusarium isolates.
  • To identify the species of Fusarium causing human infections.
  • To evaluate the efficacy of clinical antifungals and agricultural azole fungicides.

Main Methods:

  • Species identification using sequencing of the translation elongation factor 1-alpha (TEF1α) gene.
  • Antifungal susceptibility testing against amphotericin B, itraconazole, voriconazole, posaconazole, and isavuconazole.
  • Testing of azole fungicides: difenoconazole, tebuconazole, and propiconazole.

Main Results:

  • Forty-three clinical Fusarium isolates were identified, with Fusarium keratoplasticum being the most prevalent species.
  • Amphotericin B showed activity against most isolates, though with variable Minimum Inhibitory Concentrations (MICs).
  • Fusarium keratoplasticum exhibited high MICs for multiple azole antifungals, indicating resistance.

Conclusions:

  • Fusarium clinical isolates show variable susceptibility to antifungals.
  • Fusarium keratoplasticum poses a treatment challenge due to its resistance to azole antifungals.
  • Further research is needed to address emerging antifungal resistance in Fusarium infections.

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