Anuradha Chowdhary1, Anupam Prakash1, Cheshta Sharma1, Milena Kordalewska2, Anil Kumar3, Smita Sarma4, Bansidhar Tarai5, Ashutosh Singh1, Gargi Upadhyaya1, Shalini Upadhyay4, Priyanka Yadav1, Pradeep K Singh1, Vikas Khillan6, Neelam Sachdeva7, David S Perlin2, Jacques F Meis8,9. 1. Department of Medical Mycology, Vallabhbhai Patel Chest Institute, University of Delhi, Delhi, India. 2. Public Health Research Institute, Rutgers Biomedical and Health Sciences, Newark, NJ, USA. 3. Department of Microbiology, Amrita Institute of Medical Sciences and Research Center, Amrita University, Ponekkara, Cochin, India. 4. Department of Microbiology, Medanta-The Medcity, Gurgaon, Haryana, India. 5. Department of Microbiology, Max hospital, New Delhi, India. 6. Department of Microbiology, Institute of Liver & Biliary Sciences, New Delhi, India. 7. Department of Microbiology, Rajiv Gandhi Cancer Institute & Research Center, Delhi, India. 8. Department of Medical Microbiology and Infectious Diseases, Canisius-Wilhelmina Hospital, Nijmegen, The Netherlands. 9. Centre of Expertise in Mycology Radboudumc/CWZ, Nijmegen, The Netherlands.
Abstract
Background: Candida auris has emerged globally as an MDR nosocomial pathogen in ICU patients. Objectives: We studied the antifungal susceptibility of C. auris isolates (n = 350) from 10 hospitals in India collected over a period of 8 years. To investigate azole resistance, ERG11 gene sequencing and expression profiling was conducted. In addition, echinocandin resistance linked to mutations in the C. auris FKS1 gene was analysed. Methods: CLSI antifungal susceptibility testing of six azoles, amphotericin B, three echinocandins, terbinafine, 5-flucytosine and nystatin was conducted. Screening for amino acid substitutions in ERG11 and FKS1 was performed. Results: Overall, 90% of C. auris were fluconazole resistant (MICs 32 to ≥64 mg/L) and 2% and 8% were resistant to echinocandins (≥8 mg/L) and amphotericin B (≥2 mg/L), respectively. ERG11 sequences of C. auris exhibited amino acid substitutions Y132 and K143 in 77% (n = 34/44) of strains that were fluconazole resistant whereas WT genotypes, i.e. without substitutions at these positions, were observed in isolates with low fluconazole MICs (1-2 mg/L) suggesting that these substitutions confer a phenotype of resistance to fluconazole similar to that described for Candida albicans. No significant expression of ERG11 was observed, although expression was inducible in vitro with fluconazole exposure. Echinocandin resistance was linked to a novel mutation S639F in FKS1 hot spot region I. Conclusions: Overall, 25% and 13% of isolates were MDR and multi-azole resistant, respectively. The most common resistance combination was azoles and 5-flucytosine in 14% followed by azoles and amphotericin B in 7% and azoles and echinocandins in 2% of isolates.
Background: Candida auris has emerged globally as an MDR nosocomial pathogen in ICU patients. Objectives: We studied the antifungal susceptibility of C. auris isolates (n = 350) from 10 hospitals in India collected over a period of 8 years. To investigate azole resistance, ERG11 gene sequencing and expression profiling was conducted. In addition, echinocandin resistance linked to mutations in the C. auris FKS1 gene was analysed. Methods:CLSI antifungal susceptibility testing of six azoles, amphotericin B, three echinocandins, terbinafine, 5-flucytosine and nystatin was conducted. Screening for amino acid substitutions in ERG11 and FKS1 was performed. Results: Overall, 90% of C. auris were fluconazole resistant (MICs 32 to ≥64 mg/L) and 2% and 8% were resistant to echinocandins (≥8 mg/L) and amphotericin B (≥2 mg/L), respectively. ERG11 sequences of C. auris exhibited amino acid substitutions Y132 and K143 in 77% (n = 34/44) of strains that were fluconazole resistant whereas WT genotypes, i.e. without substitutions at these positions, were observed in isolates with low fluconazole MICs (1-2 mg/L) suggesting that these substitutions confer a phenotype of resistance to fluconazole similar to that described for Candida albicans. No significant expression of ERG11 was observed, although expression was inducible in vitro with fluconazole exposure. Echinocandin resistance was linked to a novel mutation S639F in FKS1 hot spot region I. Conclusions: Overall, 25% and 13% of isolates were MDR and multi-azole resistant, respectively. The most common resistance combination was azoles and 5-flucytosine in 14% followed by azoles and amphotericin B in 7% and azoles and echinocandins in 2% of isolates.
Authors: Jeffrey M Rybak; Laura A Doorley; Andrew T Nishimoto; Katherine S Barker; Glen E Palmer; P David Rogers Journal: Antimicrob Agents Chemother Date: 2019-03-27 Impact factor: 5.191
Authors: Nylev Vargas-Cruz; Ruth A Reitzel; Joel Rosenblatt; Anne-Marie Chaftari; Rita Wilson Dib; Ray Hachem; Dimitrios P Kontoyiannis; Issam I Raad Journal: Antimicrob Agents Chemother Date: 2019-06-24 Impact factor: 5.191