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In vitro antifungal susceptibilities of six antifungal drugs against clinical Candida glabrata isolates according to EUCAST
BACKGROUND AND PURPOSE: Candida glabrata is the second cause of candidiasis. The mortality rate of C. glabrata infections is about 40%; accordingly, it may be life threatening, especially in immunocompromised hosts. Regarding this, the current study was conducted to evaluate the regional patterns of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Iranian Society of Medical Mycology
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7888517/ https://www.ncbi.nlm.nih.gov/pubmed/33628974 http://dx.doi.org/10.18502/CMM.6.2.2692 |
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author | Fatahinia, Mahnaz Halvaeizadeh, Marzieh Zarei Mahmoudabadi, Ali AboualiGalehdari, Elham Kiasat, Neda |
author_facet | Fatahinia, Mahnaz Halvaeizadeh, Marzieh Zarei Mahmoudabadi, Ali AboualiGalehdari, Elham Kiasat, Neda |
author_sort | Fatahinia, Mahnaz |
collection | PubMed |
description | BACKGROUND AND PURPOSE: Candida glabrata is the second cause of candidiasis. The mortality rate of C. glabrata infections is about 40%; accordingly, it may be life threatening, especially in immunocompromised hosts. Regarding this, the current study was conducted to evaluate the regional patterns of the antifungal susceptibility of clinical C. glabrataisolated from the patients referring to the health centers located in Ahvaz, Iran MATERIALS AND METHODS: In this study, a total of 30 clinical strains of C. glabrata isolates were recovered from different body sites (i.e., vagina, mouth, and urine). Phenotypic characteristics and molecular methods were used to identify the isolates. The minimum inhibitory concentration (MIC) was determined according to the European Committee on Antimicrobial Susceptibility Testing RESULTS: Our findings demonstrated that 20%, 80%, and 6.7% of the isolates were resistant to amphotericin B, terbinafine, and posaconazole, respectively, while all the isolates were found to be fluconazole susceptible dose dependent and susceptible to voriconazole and caspofungin CONCLUSION: Our study suggested that voriconazole had high potency against C. glabrata isolates. Consequently, this antifungal agent can be an alternative drug in the treatment of resistant patients. These results can be helpful for the successful treatment of patients in different regions |
format | Online Article Text |
id | pubmed-7888517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Iranian Society of Medical Mycology |
record_format | MEDLINE/PubMed |
spelling | pubmed-78885172021-02-23 In vitro antifungal susceptibilities of six antifungal drugs against clinical Candida glabrata isolates according to EUCAST Fatahinia, Mahnaz Halvaeizadeh, Marzieh Zarei Mahmoudabadi, Ali AboualiGalehdari, Elham Kiasat, Neda Curr Med Mycol Original Article BACKGROUND AND PURPOSE: Candida glabrata is the second cause of candidiasis. The mortality rate of C. glabrata infections is about 40%; accordingly, it may be life threatening, especially in immunocompromised hosts. Regarding this, the current study was conducted to evaluate the regional patterns of the antifungal susceptibility of clinical C. glabrataisolated from the patients referring to the health centers located in Ahvaz, Iran MATERIALS AND METHODS: In this study, a total of 30 clinical strains of C. glabrata isolates were recovered from different body sites (i.e., vagina, mouth, and urine). Phenotypic characteristics and molecular methods were used to identify the isolates. The minimum inhibitory concentration (MIC) was determined according to the European Committee on Antimicrobial Susceptibility Testing RESULTS: Our findings demonstrated that 20%, 80%, and 6.7% of the isolates were resistant to amphotericin B, terbinafine, and posaconazole, respectively, while all the isolates were found to be fluconazole susceptible dose dependent and susceptible to voriconazole and caspofungin CONCLUSION: Our study suggested that voriconazole had high potency against C. glabrata isolates. Consequently, this antifungal agent can be an alternative drug in the treatment of resistant patients. These results can be helpful for the successful treatment of patients in different regions Iranian Society of Medical Mycology 2020-06 /pmc/articles/PMC7888517/ /pubmed/33628974 http://dx.doi.org/10.18502/CMM.6.2.2692 Text en Copyright: © 2020, Published by Mazandaran University of Medical Sciences on behalf of Iranian Society of Medical Mycology and Invasive Fungi Research Center. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 Unported License, ( http://creativecommons.org/licenses/by/4.0/ ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Fatahinia, Mahnaz Halvaeizadeh, Marzieh Zarei Mahmoudabadi, Ali AboualiGalehdari, Elham Kiasat, Neda In vitro antifungal susceptibilities of six antifungal drugs against clinical Candida glabrata isolates according to EUCAST |
title | In vitro antifungal susceptibilities of six antifungal drugs against clinical Candida glabrata isolates according to EUCAST |
title_full | In vitro antifungal susceptibilities of six antifungal drugs against clinical Candida glabrata isolates according to EUCAST |
title_fullStr | In vitro antifungal susceptibilities of six antifungal drugs against clinical Candida glabrata isolates according to EUCAST |
title_full_unstemmed | In vitro antifungal susceptibilities of six antifungal drugs against clinical Candida glabrata isolates according to EUCAST |
title_short | In vitro antifungal susceptibilities of six antifungal drugs against clinical Candida glabrata isolates according to EUCAST |
title_sort | in vitro antifungal susceptibilities of six antifungal drugs against clinical candida glabrata isolates according to eucast |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7888517/ https://www.ncbi.nlm.nih.gov/pubmed/33628974 http://dx.doi.org/10.18502/CMM.6.2.2692 |
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