Antimicrobial agents and chemotherapy, 2019-01, Vol.63 (1)
2019
Details
- Autor(en) / Beteiligte
- Titel
- Azole Resistance Reduces Susceptibility to the Tetrazole Antifungal VT-1161
- Ist Teil von
- Antimicrobial agents and chemotherapy, 2019-01, Vol.63 (1)
- Ort / Verlag
- United States: American Society for Microbiology
- Erscheinungsjahr
- 2019
- Link zum Volltext
- Quelle
- MEDLINE
- Beschreibungen/Notizen
- Tetrazole antifungals designed to target fungal lanosterol 14α-demethylase (LDM) appear to be effective against a range of fungal pathogens. In addition, a crystal structure of the catalytic domain of LDM in complex with the tetrazole VT-1161 has been obtained. We have addressed concern about artifacts that might arise from crystallizing VT-1161 with truncated recombinant CYP51s and measured the impact on VT-1161 susceptibility of genotypes known to confer azole resistance. A yeast system was used to overexpress recombinant full-length LDM with a C-terminal hexahistidine tag (ScLDM6×His) for phenotypic analysis and crystallographic studies with VT-1161 or with the widely used triazole drug posaconazole (PCZ). We determined the effect of characterized mutations in LDM on VT-1161 activity and identified drug efflux pumps from fungi, including key fungal pathogens, that efflux VT-1161. The relevance of these yeast-based observations on drug efflux was verified using clinical isolates of and VT-1161 binding elicits a significant conformational difference between the full-length and truncated enzymes not found when posaconazole is bound. Susceptibility to VT-1161 is reduced by ATP-binding cassette (ABC) and major facilitator superfamily (MFS) drug efflux pumps, the overexpression of LDM, and mutations within the drug binding pocket of LDM that affect interaction with the tertiary alcohol of the drug.
- Sprache
- Englisch
- Identifikatoren
- ISSN: 0066-4804eISSN: 1098-6596DOI: 10.1128/AAC.02114-18Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6325177
- Format
- –
- Schlagworte
- Amino Acid Sequence, Antifungal Agents, Antifungal Agents - chemistry, Antifungal Agents - metabolism, Antifungal Agents - pharmacology, ATP-Binding Cassette Transporters - genetics, ATP-Binding Cassette Transporters - metabolism, Candida albicans, Candida albicans - drug effects, Candida albicans - enzymology, Candida albicans - genetics, Candida albicans - growth & development, Candida glabrata, Candida glabrata - drug effects, Candida glabrata - enzymology, Candida glabrata - genetics, Candida glabrata - growth & development, Catalytic Domain, Cloning, Molecular, Crystallography, X-Ray, Drug Resistance, Fungal, Drug Resistance, Fungal - drug effects, Drug Resistance, Fungal - genetics, Experimental Therapeutics, Fungal Proteins, Fungal Proteins - chemistry, Fungal Proteins - genetics, Fungal Proteins - metabolism, Gene Expression, Genetic Vectors - chemistry, Genetic Vectors - metabolism, Microbial Sensitivity Tests, Models, Molecular, Mutation, Protein Binding, Protein Conformation, alpha-Helical, Protein Conformation, beta-Strand, Protein Interaction Domains and Motifs, Pyridines, Pyridines - chemistry, Pyridines - metabolism, Pyridines - pharmacology, Recombinant Fusion Proteins - chemistry, Recombinant Fusion Proteins - genetics, Recombinant Fusion Proteins - metabolism, Saccharomyces cerevisiae - enzymology, Saccharomyces cerevisiae - genetics, Sterol 14-Demethylase, Sterol 14-Demethylase - chemistry, Sterol 14-Demethylase - genetics, Sterol 14-Demethylase - metabolism, Substrate Specificity, Tetrazoles, Tetrazoles - chemistry, Tetrazoles - metabolism, Tetrazoles - pharmacology, Triazoles - chemistry, Triazoles - metabolism, Triazoles - pharmacology