CoERG11 A395T mutation confers azole resistance in Candida orthopsilosis clinical isolates
| Autor: | Daria Bottai, Brunella Posteraro, Antonella Lupetti, Cosmeri Rizzato, Enrica Mello, Maurizio Sanguinetti, Noemi Poma, Marina Zoppo, Arianna Tavanti |
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| Rok vydání: | 2017 |
| Předmět: |
0301 basic medicine
Microbiology (medical) Azoles Antifungal Agents Candida parapsilosis 030106 microbiology Mutant Candida orthopsilosis ERG11 A395T mutation Drug resistance Locus (genetics) Drug resistance Microbial Sensitivity Tests Biology Settore MED/07 - MICROBIOLOGIA E MICROBIOLOGIA CLINICA A395T mutation Loss of heterozygosity Fungal Proteins ERG11 03 medical and health sciences Candida orthopsilosis Drug Resistance Multiple Fungal medicine Humans Pharmacology (medical) Allele Fluconazole Pharmacology Genetics chemistry.chemical_classification Fungal genetics Candidiasis Infectious Diseases chemistry Amino Acid Substitution Mutation Azole medicine.drug |
| Zdroj: | The Journal of antimicrobial chemotherapy. 73(7) |
| ISSN: | 1460-2091 |
| Popis: | Background Candida orthopsilosis is a human fungal pathogen responsible for a wide spectrum of symptomatic infections. Evidence suggests that C. orthopsilosis is mainly susceptible to azoles, the most extensively used antifungals for treatment of these infections. However, fluconazole-resistant clinical isolates are reported. Objectives This study evaluated the contribution of a single amino acid substitution in the azole target CoErg11 to the development of azole resistance in C. orthopsilosis. Methods C. orthopsilosis clinical isolates (n = 40) were tested for their susceptibility to azoles and their CoERG11 genes were sequenced. We used a SAT1 flipper-driven transformation to integrate a mutated CoERG11 allele in the genetic background of a fluconazole-susceptible isolate. Results Susceptibility testing revealed that 16 of 40 C. orthopsilosis clinical isolates were resistant to fluconazole and to at least one other azole. We identified an A395T mutation in the CoERG11 coding sequence of azole-resistant isolates only that resulted in the non-synonymous amino acid substitution Y132F. The SAT1 flipper cassette strategy led to the creation of C. orthopsilosis mutants that carried the A395T mutation in one or both CoERG11 alleles (heterozygous or homozygous mutant, respectively) in an azole-susceptible genetic background. We tested mutant strains for azole susceptibility and for hot-spot locus heterozygosity. Both the heterozygous and the homozygous mutant strains exhibited an azole-resistant phenotype. Conclusions To the best of our knowledge, these findings provide the first evidence that the CoErg11 Y132F substitution confers multi-azole resistance in C. orthopsilosis. |
| Databáze: | OpenAIRE |
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