Molecular Characterization and Antifungal Susceptibility of Clinical Fusarium Species From Brazil

被引:57
作者
Herkert, Patricia F. [1 ,2 ,3 ]
Al-Hatmi, Abdullah M. S. [3 ,4 ,5 ]
de Oliveira Salvador, Gabriel L. [6 ]
Muro, Marisol D. [7 ]
Pinheiro, Posangela L. [7 ]
Nuccis, Marcio [8 ]
Queiroz-Telles, Flavio [9 ]
Sybren de Hoog, G. [3 ,4 ,10 ]
Meis, Jacques F. [3 ,11 ]
机构
[1] Fundacao Oswaldo Cruz, Inst Carlos Chagas, Curitiba, Parana, Brazil
[2] Inst Nacl Ciencia & Tecnol Inovacao Doencas Popul, Brasilia, DF, Brazil
[3] Ctr Expertise Mycol Radboudumc CWZ, Nijmegen, Netherlands
[4] Westerdijk Fungal Biodivers Inst, Dept Med Mycol, Utrecht, Netherlands
[5] Minist Hlth, Ibri Hosp, Directorate Gen Hlth Serv, Ibri, Oman
[6] Univ Fed Parana, Dept Internal Med, Curitiba, Parana, Brazil
[7] Univ Fed Parana, Hosp Clin, Lab Mycol, Curitiba, Parana, Brazil
[8] Univ Fed Rio de Janeiro, Univ Hosp, Dept Internal Med, Hematol Serv, Rio De Janeiro, Brazil
[9] Univ Fed Rio de Janeiro, Hosp Clin, Dept Publ Hlth, Infect Dis Unit, Rio De Janeiro, Brazil
[10] Univ Fed Parana, Postgrad Program Microbiol Parasitol & Pathol Bio, Dept Basic Pathol, Curitiba, Parana, Brazil
[11] Canisius Wilhelmina Hosp, Dept Med Microbiol & Infect Dis, Nijmegen, Netherlands
关键词
fusariosis; antifungal; fungicide; susceptibility; Fusarium; molecular identification; DNA-SEQUENCE DATABASE; INVASIVE FUSARIOSIS; HEMATOLOGIC MALIGNANCIES; PHYLOGENETIC DIVERSITY; ASPERGILLUS-FUMIGATUS; SOLANI; COMPLEX; INFECTIONS; KERATITIS; RESISTANCE;
D O I
10.3389/fmicb.2019.00737
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 (TEF1 alpha) 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 mu g mL(-1). Fusarium keratoplasticum showed high MIC values (8 > 32 mu g mL(-1)) for itraconazole, voriconazole, posaconazole, and isavuconazole. Among agricultural fungicides, difenoconazole had the lowest activity against FSSC with MICs of > 32 mu g mL(-1) for all isolates.
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