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Acquired fluconazole resistance and genetic clustering in Diutina (Candida) catenulata from clinical samples.
Nourrisson, Céline; Moniot, Maxime; Lavergne, Rose-Anne; Robert, Estelle; Bonnin, Virginie; Hagen, Ferry; Grenouillet, Frédéric; Cafarchia, Claudia; Butler, Geraldine; Cassaing, Sophie; Sabou, Marcela; Le Pape, Patrice; Poirier, Philippe; Morio, Florent.
Afiliação
  • Nourrisson C; Université Clermont Auvergne, Inserm, 3IHP, Centre Hospitalier Universitaire Clermont-Ferrand, Service de Parasitologie-Mycologie, Clermont-Ferrand, France; Université Clermont Auvergne/Inserm U1071, USC-INRAe 2018, Microbes, Intestin, Inflammation et Susceptibilité de l'Hôte, Clermont-Ferrand, Fran
  • Moniot M; Université Clermont Auvergne, Inserm, 3IHP, Centre Hospitalier Universitaire Clermont-Ferrand, Service de Parasitologie-Mycologie, Clermont-Ferrand, France.
  • Lavergne RA; Nantes Université, Centre Hospitalier Universitaire Nantes, Cibles et médicaments des infections et du cancer, IICiMed, UR 1155, Nantes, France.
  • Robert E; Nantes Université, Cibles et médicaments des infections et du cancer, IICiMed, UR 1155, Nantes, France.
  • Bonnin V; Université Clermont Auvergne/Inserm U1071, USC-INRAe 2018, Microbes, Intestin, Inflammation et Susceptibilité de l'Hôte, Clermont-Ferrand, France.
  • Hagen F; Westerdijk Fungal Biodiversity Institute, Utrecht, the Netherlands; Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, the Netherlands; Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Grenouillet F; Laboratoire de Parasitologie-Mycologie, Centre Hospitalier Universitaire Besançon, Besançon, France.
  • Cafarchia C; Dipartimento di Medicina Veterinaria, Università degli Studi 'Aldo Moro', Bari, Italy.
  • Butler G; School of Biomolecular and Biomedical Science, Conway Institute, University College Dublin, Belfield, Dublin, Ireland.
  • Cassaing S; Laboratoire de Parasitologie-Mycologie, Centre Hospitalier Universitaire Toulouse, Toulouse, France.
  • Sabou M; Laboratoire de Parasitologie et de Mycologie Médicale, Hôpitaux Universitaires de Strasbourg, Strasbourg, France; Institut de Parasitologie et de Pathologie Tropicale, UR7292 Dynamique des interactions hôte pathogène, Fédération de Médecine Translationnelle, Université de Strasbourg, Strasbourg, Fra
  • Le Pape P; Nantes Université, Centre Hospitalier Universitaire Nantes, Cibles et médicaments des infections et du cancer, IICiMed, UR 1155, Nantes, France.
  • Poirier P; Université Clermont Auvergne, Inserm, 3IHP, Centre Hospitalier Universitaire Clermont-Ferrand, Service de Parasitologie-Mycologie, Clermont-Ferrand, France; Université Clermont Auvergne/Inserm U1071, USC-INRAe 2018, Microbes, Intestin, Inflammation et Susceptibilité de l'Hôte, Clermont-Ferrand, Fran
  • Morio F; Nantes Université, Centre Hospitalier Universitaire Nantes, Cibles et médicaments des infections et du cancer, IICiMed, UR 1155, Nantes, France. Electronic address: florent.morio@chu-nantes.fr.
Clin Microbiol Infect ; 29(2): 257.e7-257.e11, 2023 Feb.
Article em En | MEDLINE | ID: mdl-36209989
OBJECTIVES: Diutina (Candida) catenulata is an ascomycetous yeast isolated from environmental sources and animals, occasionally infecting humans. The aim of this study is to shed light on the in vitro antifungal susceptibility and genetic diversity of this opportunistic yeast. METHODS: Forty-five D. catenulata strains isolated from various sources (including human and environmental sources) and originating from nine countries were included. Species identification was performed using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and confirmed via internal transcribed spacer ribosomal DNA barcoding. In vitro antifungal susceptibility was determined for seven systemic antifungals via the gradient strip method after 48 hours of incubation at 35°C using Etest® (Biomérieux) or Liofilchem® strips. Isolates exhibiting fluconazole minimal inhibitory concentrations (MICs) of ≥8 µg/mL were investigated for mutations in the ERG11 gene. A novel microsatellite genotyping scheme consisting of four markers was developed to assess genetic diversity. RESULTS: MIC ranges for amphotericin B, caspofungin, micafungin, isavuconazole, and posaconazole were 0.19-1 µg/mL, 0.094-0.5 µg/mL, 0.012-0.064 µg/mL, 0.003-0.047 µg/mL, and 0.006-0.032 µg/mL, respectively. By comparison, a broad range of MICs was noted for fluconazole (0.75 to >256 µg/mL) and voriconazole (0.012-0.38 mg/L), the higher values being observed among clinical strains. The Y132F amino acid substitution, associated with azole resistance in various Candida species (C. albicans, C. tropicalis, C. parapsilosis, and C. orthopsilosis), was the main substitution identified. Although microsatellite typing showed extensive genetic diversity, most strains with high fluconazole MICs clustered together, suggesting human-to-human transmission or a common source of contamination. DISCUSSION: The high rate of acquired fluconazole resistance among clinical isolates of D. catenulata is of concern. In this study, we highlight a link between the genetic diversity of D. catenulata and its antifungal resistance patterns, suggesting possible clonal transmission of resistant isolates.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fluconazol / Antifúngicos Limite: Animals / Humans Idioma: En Revista: Clin Microbiol Infect Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fluconazol / Antifúngicos Limite: Animals / Humans Idioma: En Revista: Clin Microbiol Infect Ano de publicação: 2023 Tipo de documento: Article