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Effect of the Novel Antifungal Drug F901318 (Olorofim) on Growth and Viability of Aspergillus fumigatus.
du Pré, Saskia; Beckmann, Nicola; Almeida, Mariana Cruz; Sibley, Graham E M; Law, Derek; Brand, Alexandra C; Birch, Mike; Read, Nick D; Oliver, Jason D.
Afiliación
  • du Pré S; F2G Ltd., Manchester, United Kingdom saskiadupre@hotmail.com.
  • Beckmann N; Manchester Fungal Infection Group, Division of Infection, Immunity and Respiratory Medicine, University of Manchester, Manchester, United Kingdom.
  • Almeida MC; F2G Ltd., Manchester, United Kingdom.
  • Sibley GEM; Aberdeen Fungal Group, MRC Centre for Medical Mycology, Institute of Medical Sciences, University of Aberdeen, Aberdeen, United Kingdom.
  • Law D; F2G Ltd., Manchester, United Kingdom.
  • Brand AC; F2G Ltd., Manchester, United Kingdom.
  • Birch M; Aberdeen Fungal Group, MRC Centre for Medical Mycology, Institute of Medical Sciences, University of Aberdeen, Aberdeen, United Kingdom.
  • Read ND; F2G Ltd., Manchester, United Kingdom.
  • Oliver JD; Manchester Fungal Infection Group, Division of Infection, Immunity and Respiratory Medicine, University of Manchester, Manchester, United Kingdom.
Article en En | MEDLINE | ID: mdl-29891595
ABSTRACT
F901318 (olorofim) is a novel antifungal drug that is highly active against Aspergillus species. Belonging to a new class of antifungals called the orotomides, F901318 targets dihydroorotate dehydrogenase (DHODH) in the de novo pyrimidine biosynthesis pathway. In this study, the antifungal effects of F901318 against Aspergillus fumigatus were investigated. Live cell imaging revealed that, at a concentration of 0.1 µg/ml, F901318 completely inhibited germination, but conidia continued to expand by isotropic growth for >120 h. When this low F901318 concentration was applied to germlings or vegetative hyphae, their elongation was completely inhibited within 10 h. Staining with the fluorescent viability dye bis-(1,3-dibutylbarbituric acid) trimethine oxonol (DiBAC) showed that prolonged exposure to F901318 (>24 h) led to vegetative hyphal swelling and a decrease in hyphal viability through cell lysis. The time-dependent killing of F901318 was further confirmed by measuring the fungal biomass and growth rate in liquid culture. The ability of hyphal growth to recover in drug-free medium after 24 h of exposure to F901318 was strongly impaired compared to that of the untreated control. A longer treatment of 48 h further improved the antifungal effect of F901318. Together, the results of this study indicate that F901318 initially has a fungistatic effect on Aspergillus isolates by inhibiting germination and growth, but prolonged exposure is fungicidal through hyphal swelling followed by cell lysis.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Piperazinas / Pirimidinas / Pirroles / Aspergillus fumigatus / Esporas Fúngicas / Hifa / Acetamidas / Antifúngicos Idioma: En Revista: Antimicrob Agents Chemother Año: 2018 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Piperazinas / Pirimidinas / Pirroles / Aspergillus fumigatus / Esporas Fúngicas / Hifa / Acetamidas / Antifúngicos Idioma: En Revista: Antimicrob Agents Chemother Año: 2018 Tipo del documento: Article País de afiliación: Reino Unido