Minimal inhibitory concentration distributions and epidemiological cutoff values of five antifungal agents against Sporothrix brasiliensis

Mem Inst Oswaldo Cruz. 2017 May;112(5):376-381. doi: 10.1590/0074-02760160527.

Abstract

Background: Sporothrix brasiliensis is the most virulent sporotrichosis agent. This species usually responds to antifungal drugs, but therapeutic failure can occur in some patients. Antifungal susceptibility tests have been performed on this species, but no clinical breakpoints (CBPs) are available. In this situation, minimal inhibitory concentration (MIC) distributions and epidemiological cutoff values (ECVs) support the detection of identification of resistant strains.

Objectives: To study the MIC distributions of five antifungal drugs against S. brasiliensis and to propose tentative ECVs.

Methods: MICs of amphotericin B (AMB), itraconazole (ITR), ketoconazole (KET), posaconazole (POS), and terbinafine (TRB) against 335 S. brasiliensis strains were determined by the Clinical and Laboratory Standards Institute broth microdilution method.

Findings: The proposed ECV, in µg/mL, for AMB, ITR, KET, POS, and TRB were 4.0, 2.0, 1.0, 2.0, and 0.25, respectively. Percentages of wild-type strains in our population for the above antifungal drugs were 98.48, 95.22, 95.33, 100, and 97.67%, respectively.

Main conclusions: These ECVs will be useful to detect strains with resistance, to define CBPs, and to elaborate specific therapeutic guidelines for S. brasiliensis. Rational use of antifungals is strongly recommended to avoid the emergence of resistant strains and ensure the therapeutic effectiveness of sporotrichosis.

Publication types

  • Comparative Study

MeSH terms

  • Amphotericin B / pharmacology
  • Animals
  • Antifungal Agents / pharmacology*
  • Cats
  • Drug Resistance, Fungal
  • Humans
  • Itraconazole / pharmacology
  • Ketoconazole / pharmacology
  • Microbial Sensitivity Tests
  • Naphthalenes / pharmacology
  • Sporothrix / drug effects*
  • Sporothrix / isolation & purification
  • Terbinafine
  • Triazoles / pharmacology

Substances

  • Antifungal Agents
  • Naphthalenes
  • Triazoles
  • Itraconazole
  • posaconazole
  • Amphotericin B
  • Terbinafine
  • Ketoconazole

Grants and funding

Financial support: FAPERJ (grant nº E-26/102.255/2013), CNPq (grants nº 305487/2015-9, 304976/2013-0), PAPES/Fiocruz (Grants 407771/2013-3, 407693/2012-2).