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Multidrug resistance in fungi: regulation of transporter-encoding gene expression
Sanjoy Paul1, W Scott Moye-Rowley1
1Department of Molecular Physiology and Biophysics, Carver College of Medicine, University of Iowa Iowa City, IA, USA.
Abstract:
A critical risk to the continued success of antifungal chemotherapy is the acquisition of resistance; a risk exacerbated by the few classes of effective antifungal drugs. Predictably, as the use of these drugs increases in the clinic, more resistant organisms can be isolated from patients. A particularly problematic form of drug resistance that routinely emerges in the major fungal pathogens is known as multidrug resistance. Multidrug resistance refers to the simultaneous acquisition of tolerance to a range of drugs via a limited or even single genetic change. This review will focus on recent progress in understanding pathways of multidrug resistance in fungi including those of most medical relevance. Analyses of multidrug resistance in Saccharomyces cerevisiae have provided the most detailed outline of multidrug resistance in a eukaryotic microorganism. Multidrug resistant isolates of S. cerevisiae typically result from changes in the activity of a pair of related transcription factors that in turn elicit overproduction of several target genes. Chief among these is the ATP-binding cassette (ABC)-encoding gene PDR5. Interestingly, in the medically important Candida species, very similar pathways are involved in acquisition of multidrug resistance. In both C. albicans and C. glabrata, changes in the activity of transcriptional activator proteins elicits overproduction of a protein closely related to S. cerevisiae Pdr5 called Cdr1. The major filamentous fungal pathogen, Aspergillus fumigatus, was previously thought to acquire resistance to azole compounds (the principal antifungal drug class) via alterations in the azole drug target-encoding gene cyp51A. More recent data indicate that pathways in addition to changes in the cyp51A gene are important determinants in A. fumigatus azole resistance. We will discuss findings that suggest azole resistance in A. fumigatus and Candida species may share more mechanistic similarities than previously thought.
Insights
Antifungal drug resistance, particularly multidrug resistance, is a growing threat in fungal infections. Understanding resistance pathways in Candida and Aspergillus species is crucial for developing new treatments.
Area of Science:
- Mycology
- Molecular Biology
- Drug Resistance
Background:
- Antifungal chemotherapy faces a significant risk from acquired drug resistance.
- Multidrug resistance, the simultaneous tolerance to multiple drugs, is a major challenge in treating fungal infections.
- Limited classes of effective antifungal drugs exacerbate this risk.
Purpose of the Study:
- To review recent advancements in understanding multidrug resistance pathways in medically relevant fungi.
- To highlight similarities and differences in resistance mechanisms across fungal species.
Main Methods:
- Review of existing literature on fungal multidrug resistance.
- Comparative analysis of resistance pathways in Saccharomyces cerevisiae, Candida species, and Aspergillus fumigatus.
Main Results:
- Multidrug resistance in Saccharomyces cerevisiae often involves transcription factors regulating ATP-binding cassette (ABC) transporters like PDR5.
- Similar pathways, involving transcriptional activators and the Cdr1 protein, are implicated in Candida species (C. albicans, C. glabrata).
- Azole resistance in Aspergillus fumigatus may involve mechanisms beyond alterations in the cyp51A gene, potentially sharing similarities with Candida species.
Conclusions:
- Fungal multidrug resistance pathways, particularly those involving ABC transporters and transcriptional regulation, show conserved mechanisms across different species.
- Further research is needed to elucidate the shared mechanistic similarities in azole resistance between Aspergillus fumigatus and Candida species.
- Understanding these pathways is critical for combating antifungal drug resistance and improving patient outcomes.
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