1. Academic Validation
  2. In vitro activity of azole derivatives and griseofulvin against planktonic and biofilm growth of clinical isolates of dermatophytes

In vitro activity of azole derivatives and griseofulvin against planktonic and biofilm growth of clinical isolates of dermatophytes

  • Mycoses. 2018 Jul;61(7):449-454. doi: 10.1111/myc.12763.
Raimunda Sâmia Nogueira Brilhante 1 Edmilson Emanuel Monteiro Correia 1 Glaucia Morgana de Melo Guedes 1 Jonathas Sales de Oliveira 1 Débora de Souza Collares Maia Castelo-Branco 1 Rossana de Aguiar Cordeiro 1 Adriana de Queiroz Pinheiro 2 Lúcio Jackson Queiroz Chaves 1 Waldemiro de Aquino Pereira Neto 1 José Júlio Costa Sidrim 1 Marcos Fábio Gadelha Rocha 1 2
Affiliations

Affiliations

  • 1 Department of Pathology and Legal Medicine, School of Medicine, Specialized Medical Mycology Center, Postgraduate Program in Medical Microbiology, Federal University of Ceará, Fortaleza, CE, Brazil.
  • 2 School of Veterinary, Postgraduate Program in Veterinary Sciences, State University of Ceará, Fortaleza, CE, Brazil.
Abstract

As shown by recent research, most of the clinically relevant fungi, including dermatophytes, form biofilms in vitro and in vivo, which may exhibit antimicrobial tolerance that favour recurrent infections. The aim of this study was to determine the minimum inhibitory concentrations (MICs) of itraconazole (ITC), voriconazole (VCZ) and griseofulvin (GRI) against Trichophyton rubrum, Trichophyton tonsurans, Trichophyton mentagrophytes, Microsporum canis and Microsporum gypseum in planktonic and biofilm growth. For the planktonic form, susceptibility testing was performed according to the Clinical and Laboratory Standards Institute (CLSI), document M38-A2, while biofilm susceptibility was evaluated using the XTT colorimetric essay. The planktonic growth of all strains was inhibited, with MIC values ranging from 0.00195 to 0.1225 μg/mL for VRC, 0.00195 to 0.25 μg/mL for ITC and <0.0039 to 4 μg/mL for GRI, while a 50-fold increase in the MIC was required to significantly reduce the metabolic activity (P < .05) of dermatophyte biofilms. In brief, the ability of dermatophytes to form biofilms may be a contributing factor for the recalcitrance of dermatophytoses or the dissemination of the disease.

Keywords

biofilm; dermatophytes; human isolates; planktonic; susceptibility testing; veterinary isolates.

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