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Antifungal Activity of a Novel Triazole, Efinaconazole and Nine Comparators against 354 Molecularly Identified Aspergillus Isolates
Management of superficial aspergillosis is a major challenge owing to the frequent relapses and treatment failure, which may pose a potential risk, thereby gradually developing resistant species. Therefore, necessitating the development of new antifungals with higher potency should be considered as...
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Published in: | Mycopathologia (1975) 2020-04, Vol.185 (2), p.357-365 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Management of superficial aspergillosis is a major challenge owing to the frequent relapses and treatment failure, which may pose a potential risk, thereby gradually developing resistant species. Therefore, necessitating the development of new antifungals with higher potency should be considered as alternative strategies for efficient management of infections. We aimed to investigate the susceptibility of
Aspergillus
isolates toward a novel triazole, efinaconazole, in comparison with various classes of antifungal drugs. Antifungal susceptibility testing was performed according to the Clinical and Laboratory Standards Institute M38-A2 guidelines. Efinaconazole exhibited poor activity against mutant
A. fumigatus
strains,
A. niger
sensu stricto, and
A. tubingensis
with GM MIC values of 3.62, 1.62, and 2 μg/ml, respectively; however, surprisingly, it efficiently inhibited the growth of
A. terreus
sensu stricto, followed by wild-type
A. fumigatus
and
A. flavus
with GM MIC values of 0.29, 0.42, and 0.52 μg/ml, respectively. Presumably, efinaconazole is inefficient in aspergillosis treatment due to the low susceptibility of
A. niger
sensu stricto
, A. tubingensis,
and mutant
A. fumigatus
; however, it may be effective in treating superficial aspergillosis caused by wild-type
A. fumigatus, A. terreus
sensu stricto, and
A. flavus
. Further studies are needed to determine how these findings may translate into in vivo efficacy. |
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ISSN: | 0301-486X 1573-0832 |
DOI: | 10.1007/s11046-020-00434-z |