Abstract

Candida albicans is an important human fungal pathogen, in terms of both its clinical significance and its use as an experimental model for scientific investigation. Although this opportunistic pathogen is a natural component of the human flora, it can cause life-threatening infections in immunosuppressed patients. There are currently a limited number of antifungal molecules and drug targets, and increasing resistance to the front-line therapeutics, demonstrating a clear need for new antifungal drugs. Understanding the biology of this pathogen is an important prerequisite for identifying new drug targets for antifungal therapeutics. In this review, we highlight some recent developments that help us to understand how virulence traits are regulated at the molecular level, in addition to technical advances that improve the ability of genome editing in C. albicans.

Highlights

  • In particular Candida albicans, represent a major component of the disease burden caused by fungi and are the fourth most common cause of nosocomial infections in North American hospitals[5]

  • This has led to increasing interest in the biology of C. albicans and a continuing improvement in the tools involved in studying this opportunistic pathogen

  • Because C. albicans is an ascomycete, a framework for understanding its biology has been provided by the model ascomycete Saccharomyces cerevisiae, arguably one of the best studied and understood eukaryotic organisms

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Summary

Invited Reviewers

F1000 Faculty Reviews are written by members of the prestigious F1000 Faculty. They are commissioned and are peer reviewed before publication to ensure that the final, published version is comprehensive and accessible. The reviewers who approved the final version are listed with their names and affiliations. Any comments on the article can be found at the end of the article

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