Molecular Characterization and Antifungal Susceptibility of Clinical Fusarium Species From Brazil
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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.
Abstract:
Fusarium is widely distributed in the environment and is involved with plant and animal diseases. In humans, several species and species complexes (SC) are related to fusariosis, i.e., F. solani SC, F. oxysporum SC, F. fujikuroi SC, F. dimerum, F. chlamydosporum, F. incarnatum-equiseti, and F. sporotrichoides. We aimed to investigate the susceptibility of Fusarium clinical isolates to antifungals and azole fungicides and identify the species. Forty-three clinical Fusarium isolates were identified by sequencing translation elongation factor 1-alpha (TEF1α) gene. Antifungal susceptibility testing was performed to the antifungals amphotericin B, itraconazole, voriconazole, posaconazole, and isavuconazole, and the azole fungicides difenoconazole, tebuconazole, and propiconazole. The isolates were recovered from patients with median age of 36 years (range 2-78 years) of which 21 were female. Disseminated fusariosis was the most frequent clinical form (n = 16, 37.2%) and acute lymphoblastic leukemia (n = 7; 16.3%) was the most commonly underlying condition. A few species described in Fusarium solani SC have recently been renamed in the genus Neocosmospora, but consistent naming is yet not possible. Fusarium keratoplasticum FSSC 2 (n = 12) was the prevalent species, followed by F. petroliphilum FSSC 1 (n = 10), N. gamsii FSSC 7 (n = 5), N. suttoniana FSSC 20 (n = 3), F. solani sensu stricto FSSC 5 (n = 2), Fusarium sp. FSSC 25 (n = 2), Fusarium sp. FSSC 35 (n = 1), Fusarium sp. FSSC18 (n = 1), F. falciforme FSSC 3+4 (n = 1), F. pseudensiforme (n = 1), and F. solani f. xanthoxyli (n = 1). Amphotericin B had activity against most isolates although MICs ranged from 0.5 to 32 μg mL-1. Fusarium keratoplasticum showed high MIC values (8->32 μg mL-1) for itraconazole, voriconazole, posaconazole, and isavuconazole. Among agricultural fungicides, difenoconazole had the lowest activity against FSSC with MICs of >32 μg mL-1 for all isolates.
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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