Abstract

Candidemia is widely reported as the fourth most common form of bloodstream infection worldwide. Reports of breakthrough cases of candidemia are increasing, especially in the context of a move away from azole antifungals as prophylactic or first line treatment toward the use of echinocandin agents. The global evaluation of echinocandin antifungal susceptibility since 2003 has included switches in testing methodologies and the move to a sentinel echinocandin approach for classification reporting. This study compiles previously unpublished data from echinocandin susceptibility testing of UK clinical isolates of C. glabrata received at the Public Health England Mycology Reference Laboratory from 2003 to 2016 and reevaluates the prevalence of resistance in light of currently accepted testing protocols. From 2015 onward, FKS gene mutation detection using a novel Pyrosequencing® assay was assessed as a predictor of echinocandin resistance alongside conventional susceptibility testing. Overall, our data show that echinocandin resistance in UK isolates of C. glabrata is a rare phenomenon and prevalence has not appreciably increased in the last 14 years. The pyrosequencing assay was able to successfully detect hot spot mutations in FKS1 and FKS2, although not all isolates that exhibited phenotypic resistance demonstrated detectable hot spot mutations. We propose that a rapid genomic based detection method for FKS mutations, as part of a multifactorial approach to susceptibility testing, could help provide accurate and timely management decisions especially in regions where echinocandin resistance has been reported to be emerging in this important pathogen.

Highlights

  • Candidaemia, which is widely reported as the fourth most common form of bloodstream infection worldwide, presents a considerable challenge to modern medicine

  • We propose that a rapid genomic based detection method for FKS mutations, as part of a multifactorial approach to susceptibility testing, could help provide accurate and timely management decisions especially in regions where echinocandin resistance has been reported to be emerging in this important pathogen

  • In total from 2003 to 2018, 7,225 clinical isolates of C. glabrata were tested for echinocandin susceptibility at the Public Health England (PHE) Mycology Reference Laboratory (MRL)

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Summary

Introduction

Candidaemia, which is widely reported as the fourth most common form of bloodstream infection worldwide, presents a considerable challenge to modern medicine. An increase in resistance to established antifungal agents and changing patient demographics are helping to widen the spectrum of species able to cause infection 1-3. Candida glabrata continues to be the second most commonly isolated cause of candidaemia after Candida albicans, with some healthcare providers indicating an increase in prevalence 7. The echinocandin antifungal class primarily consists of caspofungin (CSP), anidulafungin (ANF) and micafungin (MCF). These agents are acylated cyclic hexapeptides, which demonstrate some fungicidal activity by non-competitively inhibiting β-1, 3-glucan synthase and represent a niche class of antifungal agents for treatment of candidaemia. Breakthrough cases of infection are increasingly being reported, especially in the context of an increase in echinocandin use for prophylactic coverage or as a first line treatment alternative to fluconazole 11-16. Several studies have reported the potential for rapid acquisition of echinocandin resistance 11-12, with resistance rates as high as 13.5% observed within one US healthcare centre

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