Detection of azole resistance and ERG11 point mutations in Candida albicans isolates from tertiary hospitals in the Philippines

Candida albicans is commonly isolated from nosocomial fungal infections, and controlling these infections depends on the immune status of the patient, gravity of the infection, and the choice of the administered antifungal drug. Increasing worldwide reports of strains that are resistant to the azole...

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Main Authors: Moron, Llewelyn S., Cabrera, Esperanza C.
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Published: Animo Repository 2018
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Online Access:https://animorepository.dlsu.edu.ph/faculty_research/1783
https://animorepository.dlsu.edu.ph/context/faculty_research/article/2782/viewcontent/1.pdf
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spelling oai:animorepository.dlsu.edu.ph:faculty_research-27822023-07-21T03:19:49Z Detection of azole resistance and ERG11 point mutations in Candida albicans isolates from tertiary hospitals in the Philippines Moron, Llewelyn S. Cabrera, Esperanza C. Candida albicans is commonly isolated from nosocomial fungal infections, and controlling these infections depends on the immune status of the patient, gravity of the infection, and the choice of the administered antifungal drug. Increasing worldwide reports of strains that are resistant to the azole drugs, which are commonly used for treatment of diseases caused by C. albicans, warrant the conduct of drug susceptibility testing of clinical isolates, which is not routinely done in the Philippines. Twenty-six local C. albicans clinical isolates were tested for their susceptibility to the azole drugs fluconazole and voriconazole using the standard disc agar diffusion method. Likewise, the ERG11 gene coding for lanosterol-14-α-demethylase involved in ergosterol synthesis, which is the target of the azole drugs, was studied for the occurrence of point mutations. Results of the assay showed phenotypic resistance patterns to both drugs in 19 isolates (or 73.08%). Six isolates were determined susceptible to both drugs, while one isolate was susceptible-dose dependent also to both antifungals. Detection of ERG11 mutations following nucleotide sequencing revealed the presence of point mutations A369C, T462C and C558T. Mutations A369C and T462C have been identified as possible factors associated with the resistance to azole agents in previous studies. The results imply that it is imperative to continuously perform susceptibility testing on clinical isolates of C. albicans for effective treatment management and for the surveillance of antifungal resistance in the organism. 2018-01-01T08:00:00Z text application/pdf https://animorepository.dlsu.edu.ph/faculty_research/1783 info:doi/10.5943/cream/8/3/1 https://animorepository.dlsu.edu.ph/context/faculty_research/article/2782/viewcontent/1.pdf Faculty Research Work Animo Repository Drug resistance in microorganisms Microbial sensitivity tests Candida albicans Biology
institution De La Salle University
building De La Salle University Library
continent Asia
country Philippines
Philippines
content_provider De La Salle University Library
collection DLSU Institutional Repository
topic Drug resistance in microorganisms
Microbial sensitivity tests
Candida albicans
Biology
spellingShingle Drug resistance in microorganisms
Microbial sensitivity tests
Candida albicans
Biology
Moron, Llewelyn S.
Cabrera, Esperanza C.
Detection of azole resistance and ERG11 point mutations in Candida albicans isolates from tertiary hospitals in the Philippines
description Candida albicans is commonly isolated from nosocomial fungal infections, and controlling these infections depends on the immune status of the patient, gravity of the infection, and the choice of the administered antifungal drug. Increasing worldwide reports of strains that are resistant to the azole drugs, which are commonly used for treatment of diseases caused by C. albicans, warrant the conduct of drug susceptibility testing of clinical isolates, which is not routinely done in the Philippines. Twenty-six local C. albicans clinical isolates were tested for their susceptibility to the azole drugs fluconazole and voriconazole using the standard disc agar diffusion method. Likewise, the ERG11 gene coding for lanosterol-14-α-demethylase involved in ergosterol synthesis, which is the target of the azole drugs, was studied for the occurrence of point mutations. Results of the assay showed phenotypic resistance patterns to both drugs in 19 isolates (or 73.08%). Six isolates were determined susceptible to both drugs, while one isolate was susceptible-dose dependent also to both antifungals. Detection of ERG11 mutations following nucleotide sequencing revealed the presence of point mutations A369C, T462C and C558T. Mutations A369C and T462C have been identified as possible factors associated with the resistance to azole agents in previous studies. The results imply that it is imperative to continuously perform susceptibility testing on clinical isolates of C. albicans for effective treatment management and for the surveillance of antifungal resistance in the organism.
format text
author Moron, Llewelyn S.
Cabrera, Esperanza C.
author_facet Moron, Llewelyn S.
Cabrera, Esperanza C.
author_sort Moron, Llewelyn S.
title Detection of azole resistance and ERG11 point mutations in Candida albicans isolates from tertiary hospitals in the Philippines
title_short Detection of azole resistance and ERG11 point mutations in Candida albicans isolates from tertiary hospitals in the Philippines
title_full Detection of azole resistance and ERG11 point mutations in Candida albicans isolates from tertiary hospitals in the Philippines
title_fullStr Detection of azole resistance and ERG11 point mutations in Candida albicans isolates from tertiary hospitals in the Philippines
title_full_unstemmed Detection of azole resistance and ERG11 point mutations in Candida albicans isolates from tertiary hospitals in the Philippines
title_sort detection of azole resistance and erg11 point mutations in candida albicans isolates from tertiary hospitals in the philippines
publisher Animo Repository
publishDate 2018
url https://animorepository.dlsu.edu.ph/faculty_research/1783
https://animorepository.dlsu.edu.ph/context/faculty_research/article/2782/viewcontent/1.pdf
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