The Emerging Pathogen Candida auris: Growth Phenotype, Virulence Factors, Activity of Antifungals, and Effect of SCY-078, a Novel Glucan Synthesis Inhibitor, on Growth Morphology and Biofilm Formation

Author:

Larkin Emily1,Hager Christopher1,Chandra Jyotsna1,Mukherjee Pranab K.1,Retuerto Mauricio1,Salem Iman1,Long Lisa1,Isham Nancy1,Kovanda Laura2ORCID,Borroto-Esoda Katyna3,Wring Steve3,Angulo David3,Ghannoum Mahmoud1

Affiliation:

1. Center for Medical Mycology, Case Western Reserve University, and University Hospitals Cleveland Medical Center, Cleveland, Ohio, USA

2. Astellas Pharma Global Development, Inc., Northbrook, Illinois, USA

3. Scynexis Inc., Jersey City, New Jersey, USA

Abstract

ABSTRACT Candida auris , a new multidrug-resistant Candida spp. which is associated with invasive infection and high rates of mortality, has recently emerged. Here, we determined the virulence factors (germination, adherence, biofilm formation, phospholipase and proteinase production) of 16 C. auris isolates and their susceptibilities to 11 drugs belonging to different antifungal classes, including a novel orally bioavailable 1,3-β- d -glucan synthesis inhibitor (SCY-078). We also examined the effect of SCY-078 on the growth, ultrastructure, and biofilm-forming abilities of C. auris . Our data showed that while the tested strains did not germinate, they did produce phospholipase and proteinase in a strain-dependent manner and had a significantly reduced ability to adhere and form biofilms compared to that of Candida albicans ( P = 0.01). C. auris isolates demonstrated reduced susceptibility to fluconazole and amphotericin B, while, in general, they were susceptible to the remaining drugs tested. SCY-078 had an MIC 90 of 1 mg/liter against C. auris and caused complete inhibition of the growth of C. auris and C. albicans . Scanning electron microscopy analysis showed that SCY-078 interrupted C. auris cell division, with the organism forming abnormal fused fungal cells. Additionally, SCY-078 possessed potent antibiofilm activity, wherein treated biofilms demonstrated significantly reduced metabolic activity and a significantly reduced thickness compared to the untreated control ( P < 0.05 for both comparisons). Our study shows that C. auris expresses several virulence determinants (albeit to a lesser extent than C. albicans ) and is resistant to fluconazole and amphotericin B. SCY-078, the new orally bioavailable antifungal, had potent antifungal/antibiofilm activity against C. auris , indicating that further evaluation of this antifungal is warranted.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference54 articles.

1. Centers for Disease Control and Prevention. 24June2016, posting date. Global emergence of invasive infections caused by the multidrug-resistant yeast Candida auris. Centers for Disease Control and Prevention, Atlanta, GA. https://www.cdc.gov/fungal/diseases/candidiasis/candida-auris-alert.html . Accessed 1 July 2016.

2. Candida aurissp. nov., a novel ascomycetous yeast isolated from the external ear canal of an inpatient in a Japanese hospital

3. First Three Reported Cases of Nosocomial Fungemia Caused by Candida auris

4. New Clonal Strain ofCandida auris, Delhi, India

5. Candida auris–Associated Candidemia, South Africa

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