Mrr1 regulation of methylglyoxal catabolism and methylglyoxal‐induced fluconazole resistance in Candida lusitaniae
| Autor: | Amy R. Biermann, Elora G. Demers, Deborah A. Hogan |
|---|---|
| Rok vydání: | 2020 |
| Předmět: |
Antifungal Agents
Metabolite Gene Expression Biology Microbiology Article Sepsis Fungal Proteins 03 medical and health sciences chemistry.chemical_compound In vivo Drug Resistance Fungal Gene Expression Regulation Fungal Genes Regulator medicine Fluconazole Molecular Biology Transcription factor Gene Candida 030304 developmental biology chemistry.chemical_classification Kidney 0303 health sciences 030306 microbiology Catabolism Candida lusitaniae Methylglyoxal Candidiasis DNA Restriction Enzymes medicine.disease Pyruvaldehyde biology.organism_classification medicine.anatomical_structure chemistry Saccharomycetales Azole Efflux Transcription Factors medicine.drug |
| Zdroj: | Mol Microbiol |
| ISSN: | 1365-2958 0950-382X |
| DOI: | 10.1111/mmi.14604 |
| Popis: | InCandidaspecies, the transcription factor Mrr1 regulates azole resistance genes in addition to the expression of a suite of other genes including known and putative methylglyoxal reductases. Methylglyoxal (MG) is a toxic metabolic byproduct that is significantly elevated in certain disease states that frequently accompany candidiasis, including diabetes, kidney failure, sepsis, and inflammation. Through the genetic analysis ofCandida lusitaniae(syn.Clavispora lusitaniae) strains with different Mrr1 variants with high and low basal activity, we showed that Mrr1 regulates basal and/or induced expression of two highly similar MG reductases,MGD1andMGD2, and that both participate in MG detoxification and growth on MG as a sole carbon source. We found that exogenous MG increases Mrr1-dependent expression ofMGD1andMGD2inC. lusitaniaesuggesting that Mrr1 is part of the natural response to MG. MG also induced expression ofMDR1, which encodes a major facilitator protein involved in fluconazole resistance, in a partially Mrr1-dependent manner. MG significantly improved growth ofC. lusitaniaein the presence of fluconazole and strains with hyperactive Mrr1 variants showed greater increases in growth in the presence of fluconazole by MG. In addition to the effects of exogenous MG, we found knocking outGLO1, which encodes another MG detoxification enzyme, led to increased fluconazole resistance inC. lusitaniae. Analysis of isolates otherCandidaspecies found heterogeneity in MG resistance and MG stimulation of growth in the presence of fluconazole. Given the frequent presence of MG in human disease, we propose that induction ofMDR1in response to MG is a novel contributor toin vivoresistance of azole antifungals in multipleCandidaspecies.Author SummaryInCandidaspecies, constitutively active variants of the transcription factor Mrr1 confer resistance to fluconazole, a commonly used antifungal agent. However, the natural role of Mrr1 as well as how its activity is modulatedin vivoremain poorly understood. Here, we have shown that, in the opportunistic pathogenCandida lusitaniae, Mrr1 regulates expression and induction of two enzymes that detoxify methylglyoxal, a toxic metabolic byproduct. Importantly, serum methylglyoxal is elevated in conditions that are also associated with increased risk of colonization and infection byCandidaspecies, such as diabetes and kidney failure. We discovered that methylglyoxal causes increased expression of these two Mrr1-regulated detoxification enzymes as well as an efflux pump that causes fluconazole resistance. Likewise, methylglyoxal increased the ability of multipleC. lusitaniaestrains to grow in the presence of fluconazole. Several otherCandidastrains that we tested also exhibited stimulation of growth on fluconazole by methylglyoxal. Given the physiological relevance of methylglyoxal in human disease, we posit that the induction of fluconazole resistance in response to methylglyoxal may contribute to treatment failure. |
| Databáze: | OpenAIRE |
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