4.6 Article

Comparison of the Micronaut-AM System and the EUCAST Broth Microdilution Reference Method for MIC Determination of Four Antifungals against Aspergillus fumigatus

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JOURNAL OF FUNGI
卷 9, 期 7, 页码 -

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MDPI
DOI: 10.3390/jof9070721

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antifungal susceptibility testing; Micronaut-AM; EUCAST; Aspergillus fumigatus; cyp51A gene; azole resistance

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This study evaluated the performance of the Micronaut-AM (M-AM) system for determining the susceptibility of A. fumigatus strains to antifungal drugs and compared it with the EUCAST broth microdilution reference method. The M-AM system showed good performance for determining the Minimum Inhibitory Concentration (MIC) of amphotericin B, but further evaluations are needed for the MIC determination of azoles.
The Antifungal Susceptibility Testing method of the European Committee on Antimicrobial Susceptibility Testing (EUCAST-AFST) is a reference technique for the determination of the Minimum Inhibitory Concentration (MIC) of antifungals for Aspergillus fumigatus. However, it is time-consuming and requires expertise. Micronaut-AM (M-AM) is a fast, simple, time-saving, and ready-to-use new colorimetric method using an indicator (resazurin) to facilitate the visual reading. The aim of this retrospective study was to evaluate the performance of the M-AM system and compare it with the EUCAST broth microdilution reference method to determine the susceptibility of 77 A. fumigatus clinical strains to amphotericin B, itraconazole, voriconazole, and posaconazole. Overall, the essential agreements within & PLUSMN;2 dilutions were 100%, 62%, 58%, and 30% and the categorical agreements were 100%, 97%, 91%, and 87% for amphotericin B, itraconazole, voriconazole, and posaconazole, respectively. No categorical discrepancy was found for amphotericin B, but several categorical discordances were observed with azole antifungals. However, only 2 of the 16 azole-resistant strains confirmed by the cyp51A sequencing would have been misclassified by M-AM. The use of M-AM is probably suitable for the determination of the MICs of amphotericin B, but further evaluations are needed to confirm its usefulness for the determination of the MICs of azoles for A. fumigatus.

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