Multicenter, International Study of MIC/MEC Distributions for Definition of Epidemiological Cutoff Values for Sporothrix Species Identified by Molecular Methods

Espinel Ingroff, A. y Abreu, D. P. B. y Almeida Paes, R. y Brilhante, R. S. N. y Chakrabarti, A. y Chowdhary, A. y Hagen, F. y Córdoba, S. y González González, Gloria María y Govender, N. P. y Guarro, Josep y Johnson, E. M. y Kidd, S. E. y Pereira, S. A. y Rodrigues, A. M. y Rozental, S. y Szeszs, M. W. y Ballesté Alaniz, R. y Bonifaz, Alexandro y Bonfietti, L. X. y Borba Santos, L. P. y Capilla, Javier y Colombo, A. L. y Dolande, M. y Isla, M. G. y Melhem, M. S. C. y Mesa Arango, A. C. y Oliveira, M. M. E. y Panizo, M. M. y Pires de Camargo, Z. y Zancope Oliveira, R. M. y Meis, J. F. y Turnidge, J. (2017) Multicenter, International Study of MIC/MEC Distributions for Definition of Epidemiological Cutoff Values for Sporothrix Species Identified by Molecular Methods. Antimicrobial agents and chemotherapy, 61 (10). pp. 1-8. ISSN 0066-4804

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Resumen

ABSTRACT Clinical and Laboratory Standards Institute (CLSI) conditions for testing the susceptibilities of pathogenic Sporothrix species to antifungal agents are based on a collaborative study that evaluated five clinically relevant isolates of Sporothrix schenckii sensu lato and some antifungal agents. With the advent of molecular identification, there are two basic needs: to confirm the suitability of these testing conditions for all agents and Sporothrix species and to establish species-specific epidemiologic cutoff values (ECVs) or breakpoints (BPs) for the species. We collected available CLSI MICs/minimal effective concentrations (MECs) of amphotericin B, five triazoles, terbinafine, flucytosine, and caspofungin for 301 Sporothrix schenckii sensu stricto, 486 S. brasiliensis, 75S. globosa, and 13 S. mexicana molecularly identified isolates. Data were obtained in 17 independent laboratories (Australia, Europe, India, South Africa, and South and North America) using conidial inoculum suspensions and 48 to 72 h of incubation at 35°C. Sufficient and suitable data (modal MICs within 2-fold concentrations) allowed the proposal of the following ECVs for S. schenckii and S. brasiliensis, respectively: amphotericin B, 4 and 4 g/ml; itraconazole, 2 and 2 g/ml; posaconazole, 2 and 2 g/ml; and voriconazole, 64 and 32 g/ml. Ketoconazole and terbinafine ECVs for S. brasiliensis were 2 and 0.12 g/ml, respectively. Insufficient or unsuitable data precluded the calculation of ketoconazole and terbinafine (or any other antifungal agent) ECVs for S. schenckii, as well as ECVs for S. globosa and S. mexicana. These ECVs could aid the clinician in identifying potentially resistant isolates (non-wild type) less likely to respond to therapy.

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