AI Article Synopsis

  • The CLSI M27 guidelines are the standard protocols for testing yeast antifungal susceptibility using 96-well plates, but this setup limits the number of antifungal compounds that can be tested simultaneously.
  • With the rise of fungal resistance, there's a need for alternative methods that allow for higher throughput screening of more antifungal drugs.
  • This study introduces an optimized microdilution method using 384-well plates, which improves efficiency and consistency while validating the process with ten commonly used antifungals against specific yeast species.

Article Abstract

The Clinical and Laboratory Standards Institute (CLSI) M27 guidelines are the recommended and most commonly used protocols for broth microdilution antifungal susceptibility testing of yeasts. However, these guidelines are limited to the use of 96-well assay plates, limiting assay capacity. With the increased risk of fungal resistance emerging in the community, it is important to have alternative protocols available, that offer higher throughput and can screen more than eight to ten potential antifungal compounds per plate. This study presents an optimised broth microdilution minimum inhibitory concentration (MIC) method for testing the susceptibility of yeasts in an efficient high throughput screening setup, with minimal growth variability and maximum reproducibility. We extend the M27 guidelines and optimise the conditions for 384-well plates. Validation of the assay was performed with ten clinically used antifungals (fluconazole, amphotericin B, 5-fluorocytosine, posaconazole, voriconazole, ketoconazole, itraconazole, caspofungin diacetate, anidulafungin and micafungin) against Candida albicans and Cryptococcus neoformans.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11461513PMC
http://dx.doi.org/10.1038/s41598-024-74068-2DOI Listing

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