z-logo
open-access-imgOpen Access
Species Identification and In Vitro Antifungal Susceptibility of Aspergillus terreus Species Complex Clinical Isolates from a French Multicenter Study
Author(s) -
Sébastien Imbert,
AnneCécile Normand,
Stéphane Ranque,
J.M. Costa,
J. Guitard,
Isabelle Accoceberry,
Christine Bonnal,
Arnaud Fekkar,
Nadège BourgeoisNicolaos,
Sandrine Houzé,
Christophe Hennequin,
Renaud Piarroux,
Éric Dannaoui,
Françoise Botterel
Publication year - 2018
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.02315-17
Subject(s) - aspergillus terreus , antifungal , biology , microbiology and biotechnology , fungi imperfecti , aspergillus , in vitro , identification (biology) , multicenter study , medicine , botany , genetics , randomized controlled trial
Aspergillus sectionTerrei is a species complex currently comprised of 14 cryptic species whose prevalence in clinical samples as well as antifungal susceptibility are poorly known. The aims of this study were to investigateA. Terrei clinical isolates at the species level and to perform antifungal susceptibility analyses by reference and commercial methods. Eighty-two clinicalA. Terrei isolates were collected from 8 French university hospitals. Molecular identification was performed by sequencing parts of beta-tubulin and calmodulin genes. MICs or minimum effective concentrations (MECs) were determined for 8 antifungal drugs using both EUCAST broth microdilution (BMD) methods and concentration gradient strips (CGS). Among the 79A. Terrei isolates,A. terreus stricto sensu (n = 61),A. citrinoterreus (n = 13),A. hortai (n = 3), andA. alabamensis (n = 2) were identified. All strains had MICs of ≥1 mg/liter for amphotericin B, except for two isolates (bothA. hortai ) that had MICs of 0.25 mg/liter. FourA. terreus isolates were resistant to at least one azole drug, including one with pan-azole resistance, yet no mutation in theCYP51A gene was found. All strains had low MECs for the three echinocandins. The essential agreements (EAs) between BMD and CGS were >90%, except for those of amphotericin B (79.7%) and itraconazole (73.4%). Isolates belonging to theA . sectionTerrei identified in clinical samples show wider species diversity beyond the knownA. terreus sensu stricto . Azole resistance inside the sectionTerrei is uncommon and is not related to CYP51A mutations here. Finally, CGS is an interesting alternative for routine antifungal susceptibility testing.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom