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Multicenter, International Study of MIC/MEC Distributions for Definition of Epidemiological Cutoff Values for Sporothrix Species Identified by Molecular Methods
Author(s) -
Ana EspinelIngroff,
Daniel Paiva Barros de Abreu,
Rodrigo AlmeidaPaes,
RSN Brilhante,
Arunaloke Chakrabarti,
Anuradha Chowdhary,
Ferry Hagen,
Susana Córdoba,
Gloria M. González,
Nelesh P. Govender,
Josep Guarro,
Elizabeth M. Johnson,
Sarah Kidd,
Sandro Antônio Pereira,
Anderson Messias Rodrigues,
Sônia Rozental,
Maria Walderez Szeszs,
R. Ballesté Alaniz,
Alexandro Bonifáz,
Lucas Xavier Bonfietti,
Luana Pereira Borba-Santos,
Javier Capilla,
Arnaldo Lopes Colombo,
Maribel Dolande,
M. G. Isla,
Márcia de Souza Carvalho Melhem,
Ana Cecilia Mesa-Arango,
Manoel Marques Evangelista Oliveira,
Mercedes Panizo,
Zoilo Pires dè Camargo,
Rosely Maria ZancopéOliveira,
Jacques F. Meis,
John Turnidge
Publication year - 2017
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.01057-17
Subject(s) - terbinafine , posaconazole , itraconazole , biology , microbiology and biotechnology , sporothrix schenckii , amphotericin b , voriconazole , caspofungin , antifungal , sporotrichosis , immunology
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 , 75 S. 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 μg/ml; itraconazole, 2 and 2 μg/ml; posaconazole, 2 and 2 μg/ml; and voriconazole, 64 and 32 μg/ml. Ketoconazole and terbinafine ECVs for S. brasiliensis were 2 and 0.12 μg/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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