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Identification and Antifungal Drug Susceptibility Pattern of Candida auris in India

INTRODUCTION: Candida auris has turned up as a multidrug-resistant nosocomial agent with outbreaks reported worldwide. The present study was conducted to evaluate the antifungal drug susceptibility pattern of C. auris. METHODS: Isolates of C. auris were obtained from clinically suspected cases of ca...

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Autores principales: Deshkar, Smita, Patil, Niranjan, Amberkar, Shraddha, Lad, Ashish, Siddiqui, Farozan, Sharan, Swati
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9831210/
https://www.ncbi.nlm.nih.gov/pubmed/36636301
http://dx.doi.org/10.4103/jgid.jgid_44_22
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author Deshkar, Smita
Patil, Niranjan
Amberkar, Shraddha
Lad, Ashish
Siddiqui, Farozan
Sharan, Swati
author_facet Deshkar, Smita
Patil, Niranjan
Amberkar, Shraddha
Lad, Ashish
Siddiqui, Farozan
Sharan, Swati
author_sort Deshkar, Smita
collection PubMed
description INTRODUCTION: Candida auris has turned up as a multidrug-resistant nosocomial agent with outbreaks reported worldwide. The present study was conducted to evaluate the antifungal drug susceptibility pattern of C. auris. METHODS: Isolates of C. auris were obtained from clinically suspected cases of candidemia from January 2019 to June 2021. Identification was done with matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) and panfungal DNA polymerase chain reaction (PCR), followed by sequencing. Antifungal susceptibility testing was performed with broth microdilution method. RESULTS: Out of 50 isolates C. auris, 49 were identified by MALDI-TOF and one isolate was identified with panfungal DNA PCR followed by sequencing. For fluconazole, 84% (n = 42) isolates were found to be resistant and 16% (n = 8) isolates were susceptible (minimum inhibitory concentrations [MICs] range 0.5–16). Posaconazole exhibited potent activity, followed by itraconazole. For amphotericin B, only 6% (n = 3) isolates were resistant with MICs ≥2 μg/mL. Only 4% (n = 2) isolates exhibited resistance to caspofungin. No resistance was noted for micafungin and anidulafungin. One (2%) isolate was found to be panazole resistant. One (2%) isolate was resistant to fluconazole, amphotericin B, and caspofungin. CONCLUSION: Correct identification of C. auris can be obtained with the use of MALDI-TOF and sequencing methods. A small percentage of fluconazole-sensitive isolates are present. Although elevated MICs for amphotericin B and echinocandins are not generally observed, the possibility of resistance with the irrational use of these antifungal drugs cannot be denied. Pan azole-resistant and pan drug-resistant strains of C. auris are on rise.
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spelling pubmed-98312102023-01-11 Identification and Antifungal Drug Susceptibility Pattern of Candida auris in India Deshkar, Smita Patil, Niranjan Amberkar, Shraddha Lad, Ashish Siddiqui, Farozan Sharan, Swati J Glob Infect Dis Original Article INTRODUCTION: Candida auris has turned up as a multidrug-resistant nosocomial agent with outbreaks reported worldwide. The present study was conducted to evaluate the antifungal drug susceptibility pattern of C. auris. METHODS: Isolates of C. auris were obtained from clinically suspected cases of candidemia from January 2019 to June 2021. Identification was done with matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) and panfungal DNA polymerase chain reaction (PCR), followed by sequencing. Antifungal susceptibility testing was performed with broth microdilution method. RESULTS: Out of 50 isolates C. auris, 49 were identified by MALDI-TOF and one isolate was identified with panfungal DNA PCR followed by sequencing. For fluconazole, 84% (n = 42) isolates were found to be resistant and 16% (n = 8) isolates were susceptible (minimum inhibitory concentrations [MICs] range 0.5–16). Posaconazole exhibited potent activity, followed by itraconazole. For amphotericin B, only 6% (n = 3) isolates were resistant with MICs ≥2 μg/mL. Only 4% (n = 2) isolates exhibited resistance to caspofungin. No resistance was noted for micafungin and anidulafungin. One (2%) isolate was found to be panazole resistant. One (2%) isolate was resistant to fluconazole, amphotericin B, and caspofungin. CONCLUSION: Correct identification of C. auris can be obtained with the use of MALDI-TOF and sequencing methods. A small percentage of fluconazole-sensitive isolates are present. Although elevated MICs for amphotericin B and echinocandins are not generally observed, the possibility of resistance with the irrational use of these antifungal drugs cannot be denied. Pan azole-resistant and pan drug-resistant strains of C. auris are on rise. Wolters Kluwer - Medknow 2022-11-01 /pmc/articles/PMC9831210/ /pubmed/36636301 http://dx.doi.org/10.4103/jgid.jgid_44_22 Text en Copyright: © 2022 Journal of Global Infectious Diseases https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Deshkar, Smita
Patil, Niranjan
Amberkar, Shraddha
Lad, Ashish
Siddiqui, Farozan
Sharan, Swati
Identification and Antifungal Drug Susceptibility Pattern of Candida auris in India
title Identification and Antifungal Drug Susceptibility Pattern of Candida auris in India
title_full Identification and Antifungal Drug Susceptibility Pattern of Candida auris in India
title_fullStr Identification and Antifungal Drug Susceptibility Pattern of Candida auris in India
title_full_unstemmed Identification and Antifungal Drug Susceptibility Pattern of Candida auris in India
title_short Identification and Antifungal Drug Susceptibility Pattern of Candida auris in India
title_sort identification and antifungal drug susceptibility pattern of candida auris in india
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9831210/
https://www.ncbi.nlm.nih.gov/pubmed/36636301
http://dx.doi.org/10.4103/jgid.jgid_44_22
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