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Lack of Association between Fluconazole Susceptibility and ERG11 Nucleotide Polymorphisms in Cryptococcus neoformans Clinical Isolates from Uganda

Fluconazole is the drug of choice for cryptococcal meningitis (CM) monoprophylaxis in resource-limited settings such as Uganda. Emerging fluconazole resistance linked to mutations in the Cryptococcus neoformans ERG11 gene (CYP51) has been observed in clinical isolates. Currently, the single nucleoti...

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Autores principales: Atim, Priscilla Belbir, Meya, David B., Gerlach, Elliot S., Muhanguzi, Dennis, Male, Allan, Kanamwanji, Benedict, Nielsen, Kirsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9145384/
https://www.ncbi.nlm.nih.gov/pubmed/35628763
http://dx.doi.org/10.3390/jof8050508
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author Atim, Priscilla Belbir
Meya, David B.
Gerlach, Elliot S.
Muhanguzi, Dennis
Male, Allan
Kanamwanji, Benedict
Nielsen, Kirsten
author_facet Atim, Priscilla Belbir
Meya, David B.
Gerlach, Elliot S.
Muhanguzi, Dennis
Male, Allan
Kanamwanji, Benedict
Nielsen, Kirsten
author_sort Atim, Priscilla Belbir
collection PubMed
description Fluconazole is the drug of choice for cryptococcal meningitis (CM) monoprophylaxis in resource-limited settings such as Uganda. Emerging fluconazole resistance linked to mutations in the Cryptococcus neoformans ERG11 gene (CYP51) has been observed in clinical isolates. Currently, the single nucleotide polymorphisms [SNPs] in the Cryptococcus spp. ERG11 gene that could be responsible for fluconazole resistance are poorly characterized within Ugandan C. neoformans clinical isolates. If available, this information would be useful in the management of cryptococcosis among HIV patients. This cross-sectional study investigates the SNPs present in the coding region of the C. neoformans ERG11 gene to determine the relationship between the SNPs identified and fluconazole susceptibility of the clinical isolates. 310 C. neoformans isolates recovered from the Cerebrospinal Fluid (CSF) of patients with HIV and cryptococcal meningitis were examined. The fluconazole half-maximal inhibitory concentrations (IC(50) range: 0.25–32 μg/mL) was determined using the microbroth dilution method. A total of 56.1% of the isolates had low IC(50) values of <8 μg/mL while 43.9% had high IC(50) values ≥ 8 μg/mL. We amplified and sequenced 600 bp of the ERG11 coding sequence from 40 of the clinical isolates. Novel synonymous and 2 missense mutations, S460T and A457V, were identified in the ERG11 gene. The identified SNPs were not associated with differences in fluconazole IC(50) values in vitro (p = 0.179).
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spelling pubmed-91453842022-05-29 Lack of Association between Fluconazole Susceptibility and ERG11 Nucleotide Polymorphisms in Cryptococcus neoformans Clinical Isolates from Uganda Atim, Priscilla Belbir Meya, David B. Gerlach, Elliot S. Muhanguzi, Dennis Male, Allan Kanamwanji, Benedict Nielsen, Kirsten J Fungi (Basel) Article Fluconazole is the drug of choice for cryptococcal meningitis (CM) monoprophylaxis in resource-limited settings such as Uganda. Emerging fluconazole resistance linked to mutations in the Cryptococcus neoformans ERG11 gene (CYP51) has been observed in clinical isolates. Currently, the single nucleotide polymorphisms [SNPs] in the Cryptococcus spp. ERG11 gene that could be responsible for fluconazole resistance are poorly characterized within Ugandan C. neoformans clinical isolates. If available, this information would be useful in the management of cryptococcosis among HIV patients. This cross-sectional study investigates the SNPs present in the coding region of the C. neoformans ERG11 gene to determine the relationship between the SNPs identified and fluconazole susceptibility of the clinical isolates. 310 C. neoformans isolates recovered from the Cerebrospinal Fluid (CSF) of patients with HIV and cryptococcal meningitis were examined. The fluconazole half-maximal inhibitory concentrations (IC(50) range: 0.25–32 μg/mL) was determined using the microbroth dilution method. A total of 56.1% of the isolates had low IC(50) values of <8 μg/mL while 43.9% had high IC(50) values ≥ 8 μg/mL. We amplified and sequenced 600 bp of the ERG11 coding sequence from 40 of the clinical isolates. Novel synonymous and 2 missense mutations, S460T and A457V, were identified in the ERG11 gene. The identified SNPs were not associated with differences in fluconazole IC(50) values in vitro (p = 0.179). MDPI 2022-05-15 /pmc/articles/PMC9145384/ /pubmed/35628763 http://dx.doi.org/10.3390/jof8050508 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Atim, Priscilla Belbir
Meya, David B.
Gerlach, Elliot S.
Muhanguzi, Dennis
Male, Allan
Kanamwanji, Benedict
Nielsen, Kirsten
Lack of Association between Fluconazole Susceptibility and ERG11 Nucleotide Polymorphisms in Cryptococcus neoformans Clinical Isolates from Uganda
title Lack of Association between Fluconazole Susceptibility and ERG11 Nucleotide Polymorphisms in Cryptococcus neoformans Clinical Isolates from Uganda
title_full Lack of Association between Fluconazole Susceptibility and ERG11 Nucleotide Polymorphisms in Cryptococcus neoformans Clinical Isolates from Uganda
title_fullStr Lack of Association between Fluconazole Susceptibility and ERG11 Nucleotide Polymorphisms in Cryptococcus neoformans Clinical Isolates from Uganda
title_full_unstemmed Lack of Association between Fluconazole Susceptibility and ERG11 Nucleotide Polymorphisms in Cryptococcus neoformans Clinical Isolates from Uganda
title_short Lack of Association between Fluconazole Susceptibility and ERG11 Nucleotide Polymorphisms in Cryptococcus neoformans Clinical Isolates from Uganda
title_sort lack of association between fluconazole susceptibility and erg11 nucleotide polymorphisms in cryptococcus neoformans clinical isolates from uganda
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9145384/
https://www.ncbi.nlm.nih.gov/pubmed/35628763
http://dx.doi.org/10.3390/jof8050508
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