Reduced Susceptibility to Azoles in Cryptococcus gattii Correlates with the Substitution R258L in a Substrate Recognition Site of the Lanosterol 14-?-Demethylase

Cryptococcus neoformans and Cryptococcus gattii cause cryptococcosis, a lifethreatening fungal infection affecting mostly immunocompromised patients. In fact, cryptococcal meningitis accounts for about 19% of AIDS-related deaths in the world. Because of long-term azole therapies to treat this mycosi...

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Fecha de publicación:
2023
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/42188
Acceso en línea:
https://repository.urosario.edu.co/handle/10336/42188
Palabra clave:
Colombia
Cryptococcosis
Cryptococcus neoformans
Cryptococcus gattii
ERG11
Fluconazole resistance
Antimicrobial resistance
Azole resistance
Voriconazole
Rights
License
Attribution-NonCommercial-ShareAlike 4.0 International
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spelling b78cdb6d-9c3c-4868-a0f7-fddab71b0dcdd741f9a5-e889-4772-b308-36a9b848f8ba4004b1785ee-53ef-4121-be5f-a0483a46b241528186962024-01-31T19:05:26Z2024-01-31T19:05:26Z2023-08-172023Cryptococcus neoformans and Cryptococcus gattii cause cryptococcosis, a lifethreatening fungal infection affecting mostly immunocompromised patients. In fact, cryptococcal meningitis accounts for about 19% of AIDS-related deaths in the world. Because of long-term azole therapies to treat this mycosis, resistance to fluconazole leading to treatment failure and poor prognosis has long been reported for both fungal species. Among the mechanisms implicated in resistance to azoles, mutations in the ERG11 gene, encoding the azole target enzyme lanosterol 14-a-demethylase, have been described. This study aimed to establish the amino acid composition of ERG11 of Colombian clinical isolates of C. neoformans and C. gattii and to correlate any possible substitution with the in vitro susceptibility profile of the isolates to fluconazole, voriconazole, and itraconazole. Antifungal susceptibility testing results showed that C. gattii isolates are less susceptible to azoles than C. neoformans isolates, which could correlate with differences in the amino acid composition and structure of ERG11 of each species. In addition, in a C. gattii isolate with high MICs for fluconazole (64 mg/mL) and voriconazole (1 mg/mL), a G973T mutation resulting in the substitution R258L, located in substrate recognition site 3 of ERG11, was identified. This finding suggests the association of the newly reported substitution with the azole resistance phenotype in C. gattii. Further investigations are needed to determine the exact role that R258L plays in the decreased susceptibility to fluconazole and voriconazole, as well as to determine the participation of additional mechanisms of resistance to azole drugs.application/pdf10.1128/spectrum.01403-23https://repository.urosario.edu.co/handle/10336/42188engUniversidad del Rosariohttps://journals.asm.org/doi/10.1128/spectrum.01403-23Attribution-NonCommercial-ShareAlike 4.0 InternationalAbierto (Texto Completo)https://creativecommons.org/licenses/by/4.0/http://purl.org/coar/access_right/c_abf2Microbiology spectruminstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURColombiaCryptococcosisCryptococcus neoformansCryptococcus gattiiERG11Fluconazole resistanceAntimicrobial resistanceAzole resistanceVoriconazoleReduced Susceptibility to Azoles in Cryptococcus gattii Correlates with the Substitution R258L in a Substrate Recognition Site of the Lanosterol 14-?-DemethylasearticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Carvajal, Silvia KatherineEscandón, PatriciaFiracative Ropero, Sandra CarolinaORIGINALReduced Susceptibility to Azoles.pdfapplication/pdf2195366https://repository.urosario.edu.co/bitstreams/612dd9ce-5183-4c99-94f4-05199cf7807d/downloada389dc4ee5be9170bd3c5f8cc603e8d9MD51TEXTReduced Susceptibility to Azoles.pdf.txtReduced Susceptibility to Azoles.pdf.txtExtracted texttext/plain68125https://repository.urosario.edu.co/bitstreams/093b053d-64c0-4120-8de7-b5b7a9338e43/download21e9a0161e1c4551b5e40f74243768c5MD52THUMBNAILReduced Susceptibility to Azoles.pdf.jpgReduced Susceptibility to Azoles.pdf.jpgGenerated Thumbnailimage/jpeg4261https://repository.urosario.edu.co/bitstreams/791f3f58-d895-4925-8766-f96df40b7d87/download5fce2900ef7502cccf6403fc02f92316MD5310336/42188oai:repository.urosario.edu.co:10336/421882024-02-01 03:00:54.0https://creativecommons.org/licenses/by/4.0/Attribution-NonCommercial-ShareAlike 4.0 Internationalhttps://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Reduced Susceptibility to Azoles in Cryptococcus gattii Correlates with the Substitution R258L in a Substrate Recognition Site of the Lanosterol 14-?-Demethylase
title Reduced Susceptibility to Azoles in Cryptococcus gattii Correlates with the Substitution R258L in a Substrate Recognition Site of the Lanosterol 14-?-Demethylase
spellingShingle Reduced Susceptibility to Azoles in Cryptococcus gattii Correlates with the Substitution R258L in a Substrate Recognition Site of the Lanosterol 14-?-Demethylase

Colombia
Cryptococcosis
Cryptococcus neoformans
Cryptococcus gattii
ERG11
Fluconazole resistance
Antimicrobial resistance
Azole resistance
Voriconazole
title_short Reduced Susceptibility to Azoles in Cryptococcus gattii Correlates with the Substitution R258L in a Substrate Recognition Site of the Lanosterol 14-?-Demethylase
title_full Reduced Susceptibility to Azoles in Cryptococcus gattii Correlates with the Substitution R258L in a Substrate Recognition Site of the Lanosterol 14-?-Demethylase
title_fullStr Reduced Susceptibility to Azoles in Cryptococcus gattii Correlates with the Substitution R258L in a Substrate Recognition Site of the Lanosterol 14-?-Demethylase
title_full_unstemmed Reduced Susceptibility to Azoles in Cryptococcus gattii Correlates with the Substitution R258L in a Substrate Recognition Site of the Lanosterol 14-?-Demethylase
title_sort Reduced Susceptibility to Azoles in Cryptococcus gattii Correlates with the Substitution R258L in a Substrate Recognition Site of the Lanosterol 14-?-Demethylase
dc.creator.spa.fl_str_mv
author
author_facet
author_role author
dc.subject.spa.fl_str_mv Colombia
Cryptococcosis
Cryptococcus neoformans
Cryptococcus gattii
ERG11
Fluconazole resistance
Antimicrobial resistance
Azole resistance
Voriconazole
topic Colombia
Cryptococcosis
Cryptococcus neoformans
Cryptococcus gattii
ERG11
Fluconazole resistance
Antimicrobial resistance
Azole resistance
Voriconazole
description Cryptococcus neoformans and Cryptococcus gattii cause cryptococcosis, a lifethreatening fungal infection affecting mostly immunocompromised patients. In fact, cryptococcal meningitis accounts for about 19% of AIDS-related deaths in the world. Because of long-term azole therapies to treat this mycosis, resistance to fluconazole leading to treatment failure and poor prognosis has long been reported for both fungal species. Among the mechanisms implicated in resistance to azoles, mutations in the ERG11 gene, encoding the azole target enzyme lanosterol 14-a-demethylase, have been described. This study aimed to establish the amino acid composition of ERG11 of Colombian clinical isolates of C. neoformans and C. gattii and to correlate any possible substitution with the in vitro susceptibility profile of the isolates to fluconazole, voriconazole, and itraconazole. Antifungal susceptibility testing results showed that C. gattii isolates are less susceptible to azoles than C. neoformans isolates, which could correlate with differences in the amino acid composition and structure of ERG11 of each species. In addition, in a C. gattii isolate with high MICs for fluconazole (64 mg/mL) and voriconazole (1 mg/mL), a G973T mutation resulting in the substitution R258L, located in substrate recognition site 3 of ERG11, was identified. This finding suggests the association of the newly reported substitution with the azole resistance phenotype in C. gattii. Further investigations are needed to determine the exact role that R258L plays in the decreased susceptibility to fluconazole and voriconazole, as well as to determine the participation of additional mechanisms of resistance to azole drugs.
publishDate 2023
dc.date.created.spa.fl_str_mv 2023-08-17
dc.date.issued.spa.fl_str_mv 2023
dc.date.accessioned.none.fl_str_mv 2024-01-31T19:05:26Z
dc.date.available.none.fl_str_mv 2024-01-31T19:05:26Z
dc.type.spa.fl_str_mv article
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dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.spa.fl_str_mv 10.1128/spectrum.01403-23
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/42188
identifier_str_mv 10.1128/spectrum.01403-23
url https://repository.urosario.edu.co/handle/10336/42188
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.uri.spa.fl_str_mv https://journals.asm.org/doi/10.1128/spectrum.01403-23
dc.rights.spa.fl_str_mv Attribution-NonCommercial-ShareAlike 4.0 International
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dc.rights.acceso.spa.fl_str_mv Abierto (Texto Completo)
dc.rights.uri.spa.fl_str_mv https://creativecommons.org/licenses/by/4.0/
rights_invalid_str_mv Attribution-NonCommercial-ShareAlike 4.0 International
Abierto (Texto Completo)
https://creativecommons.org/licenses/by/4.0/
http://purl.org/coar/access_right/c_abf2
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dc.source.spa.fl_str_mv Microbiology spectrum
institution Universidad del Rosario
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