Aspergillus spp.: suscetibilidade aos antifúngicos isolados e em associação por diferentes metodologias e detecção de mecanismos de resistência a azólicos

Detalhes bibliográficos
Autor(a) principal: Denardi, Laura Bedin
Data de Publicação: 2018
Tipo de documento: Tese
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
dARK ID: ark:/26339/0013000000qt9
Texto Completo: http://repositorio.ufsm.br/handle/1/20458
Resumo: Aspergillosis is a group of diseases among the main causes of morbidity and mortality in immunosuppressed patients. Aspergillus fumigatus is the most common species that causes invasive and non-invasive aspergillosis in humans, followed by Aspergillus flavus, Aspergillus niger and Aspergillus terreus. Azole antifungals are the main treatment of these infections, with voriconazole being the drug of choice in invasive aspergillosis. Echinocandins and amphotericin B are also active against Aspergillus and are currently used in specific situations or in association with azoles. Azole resistance has been increasingly documented among medical centers around the world, mainly associated with A. fumigatus, and has become a major therapeutic problem. The development of resistance has been associated with mutations in the cyp51A gene of A. fumigatus. Two pathways of resistance selection have been studied, the pathway in the patient, and more recently, an environmental route. In order to overcome resistance, alternatives such as the use of combination drugs have been studied in the treatment of patients with aspergillosis refractory to standard treatment. This study aimed to determine the susceptibility profile of A. fumigatus and A. flavus, isolated from patients with aspergillosis or from the environment against azole antifungals, echinocandins and amphotericin B, alone and in combination, by using different methodologies. In addition, resistance mechanisms of clinical or environmental strains of A. fumigatus that showed resistance to one or more azole antifungals were investigated. The main results showed that in either environmental or clinical strains some azole resistant profiles were detected, while the echinocandins were very active against both species of Aspergillus. Amphotericin B showed more pronounced activity against A. fumigatus in comparison to A. flavus. In addition, Etest and agar plates with azole methodologies have been found to be capable of determining the minimum inhibitory concentration (MIC) and detecting resistance of A. fumigatus to isavuconazole, respectively, in accordance with the standard broth microdilution method. The interactions between azole and echinocandin antifungal agents against A. fumigatus varied depending on the methodology used, making it very important to standardize these methods to obtain concordant results. However, the synergistic interactions found in vitro and in vivo showed a favorable effect to the use of these associations in the treatment of aspergillosis. In the azole-echinocandin combinations against A. flavus, a higher percentage of synergistic interactions were observed when the MIC was read while by reading the minimum effective concentration (MEC) indifference was the main outcome. Furthermore, mutations linked to the cyp51A gene were found in one clinical and one environmental itraconazole-resistant A. fumigatus strains. In conclusion, combinations between azoles and echinocandins are promising for use in the treatment of patients with aspergillosis refractory to standard treatment; different Aspergillus susceptibility profiles to antifungals tested alone and in association can be found depending on the methodology used, making it necessary to standardize the different tests in order to have easier and faster methodologies that facilitate their use in routine laboratories. Finally, the first report of the presence of mechanisms of resistance to azoles linked to the cyp51A gene in Brazilian Aspergillus isolates generates concern with the management of aspergillosis in clinical centers of Brazil in order to avoid that the resistance rates increase by the indiscriminate use of azoles in the clinic and in agriculture.
id UFSM_385219c718213c6636c6639acaf00123
oai_identifier_str oai:repositorio.ufsm.br:1/20458
network_acronym_str UFSM
network_name_str Manancial - Repositório Digital da UFSM
repository_id_str
spelling Aspergillus spp.: suscetibilidade aos antifúngicos isolados e em associação por diferentes metodologias e detecção de mecanismos de resistência a azólicosAspergillus spp.: susceptibility to antifungal drugs alone and in combination using different methodologies and detection of azole resistance mechanismsAspergillus spp.Resistência a azólicosInterações entre antifúngicosAspergilosisAzole ResistanceAntifungal interactionsAspergillosisCNPQ::CIENCIAS DA SAUDE::FARMACIAAspergillosis is a group of diseases among the main causes of morbidity and mortality in immunosuppressed patients. Aspergillus fumigatus is the most common species that causes invasive and non-invasive aspergillosis in humans, followed by Aspergillus flavus, Aspergillus niger and Aspergillus terreus. Azole antifungals are the main treatment of these infections, with voriconazole being the drug of choice in invasive aspergillosis. Echinocandins and amphotericin B are also active against Aspergillus and are currently used in specific situations or in association with azoles. Azole resistance has been increasingly documented among medical centers around the world, mainly associated with A. fumigatus, and has become a major therapeutic problem. The development of resistance has been associated with mutations in the cyp51A gene of A. fumigatus. Two pathways of resistance selection have been studied, the pathway in the patient, and more recently, an environmental route. In order to overcome resistance, alternatives such as the use of combination drugs have been studied in the treatment of patients with aspergillosis refractory to standard treatment. This study aimed to determine the susceptibility profile of A. fumigatus and A. flavus, isolated from patients with aspergillosis or from the environment against azole antifungals, echinocandins and amphotericin B, alone and in combination, by using different methodologies. In addition, resistance mechanisms of clinical or environmental strains of A. fumigatus that showed resistance to one or more azole antifungals were investigated. The main results showed that in either environmental or clinical strains some azole resistant profiles were detected, while the echinocandins were very active against both species of Aspergillus. Amphotericin B showed more pronounced activity against A. fumigatus in comparison to A. flavus. In addition, Etest and agar plates with azole methodologies have been found to be capable of determining the minimum inhibitory concentration (MIC) and detecting resistance of A. fumigatus to isavuconazole, respectively, in accordance with the standard broth microdilution method. The interactions between azole and echinocandin antifungal agents against A. fumigatus varied depending on the methodology used, making it very important to standardize these methods to obtain concordant results. However, the synergistic interactions found in vitro and in vivo showed a favorable effect to the use of these associations in the treatment of aspergillosis. In the azole-echinocandin combinations against A. flavus, a higher percentage of synergistic interactions were observed when the MIC was read while by reading the minimum effective concentration (MEC) indifference was the main outcome. Furthermore, mutations linked to the cyp51A gene were found in one clinical and one environmental itraconazole-resistant A. fumigatus strains. In conclusion, combinations between azoles and echinocandins are promising for use in the treatment of patients with aspergillosis refractory to standard treatment; different Aspergillus susceptibility profiles to antifungals tested alone and in association can be found depending on the methodology used, making it necessary to standardize the different tests in order to have easier and faster methodologies that facilitate their use in routine laboratories. Finally, the first report of the presence of mechanisms of resistance to azoles linked to the cyp51A gene in Brazilian Aspergillus isolates generates concern with the management of aspergillosis in clinical centers of Brazil in order to avoid that the resistance rates increase by the indiscriminate use of azoles in the clinic and in agriculture.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESAs aspergiloses aparecem entre as principais causas de morbidade e mortalidade em pacientes em estado de imunossupressão. Aspergillus fumigatus é a espécie mais comum causadora de aspergilose invasiva e não-invasiva em humanos, seguida de Aspergillus flavus, Aspergillus niger e Aspergillus terreus. O tratamento destas infecções é efetuado principalmente através da administração de antifúngicos azólicos, sendo voriconazol o fármaco de escolha na aspergilose invasiva. Equinocandinas e anfotericina B também são ativas frente a Aspergillus e são atualmente utilizadas em situações específicas ou em associação a azólicos. Resistência aos azólicos tem sido documentada de forma crescente entre os centros médicos pelo mundo, principalmente associada a A. fumigatus, e vem se tornando um problema terapêutico de grande relevância. O desenvolvimento de resistência tem sido associado a mutações no gene cyp51A de A. fumigatus. Duas vias de seleção de resistência têm sido estudadas, a via no paciente, e mais recentemente, uma rota ambiental. Com o objetivo de superar a resistência, vem se estudando alternativas, como o uso de fármacos combinados no tratamento de pacientes com aspergilose refratária ao tratamento padrão. Neste estudo buscou-se determinar o perfil de suscetibilidade de A. fumigatus e A. flavus, isolados de pacientes com aspergilose ou do ambiente, frente aos antifúngicos azólicos, equinocandinas e anfotericina B, bem como frente a associações destes por diferentes metodologias. Além disso, foram investigados os mecanismos de resistência de A. fumigatus de origem clínica ou ambiental que apresentaram resistência a um ou mais antifúngicos azólicos. Os principais resultados observados mostraram que tanto nos isolados ambientais quanto nos clínicos alguns perfis resistentes a azólicos foram detectados, enquanto que as equinocandinas mostraram-se bastante ativas frente as duas espécies de Aspergillus e a anfotericina B mostrou atividade mais pronunciada frente a A. fumigatus do que a A. flavus. Além disso, verificou-se que as metodologias de Etest e crescimento em ágar contendo azólicos são capazes de determinar a concentração inibitória mínima (CIM) e detectar resistência de A. fumigatus ao isavuconazol, respectivamente, em concordância com a metodologia padrão de microdiluição em caldo. As interações entre antifúngicos azólicos e equinocandinas frente a A. fumigatus variaram dependendo da metodologia empregada, tornando-se muito importante a padronização destes métodos para obtenção de resultados concordantes. Contudo, as interações sinérgicas encontradas in vitro e in vivo mostram um efeito favorável ao uso destas associações no tratamento das aspergiloses. Nas combinações de azólicos e equinocandinas frente a A. flavus, uma maior porcentagem de interações sinérgicas foi observada utilizando como base a leitura da CIM, enquanto que pela leitura da concentração efetiva mínima (CEM) indiferença foi o principal resultado. Ainda, verificou-se a presença de mutações ligadas ao gene cyp51A em uma cepa clínica e em uma ambiental de A. fumigatus resistentes ao itraconazol, descritas pela primeira vez no Brasil. Conclui-se que as combinações entre azólicos e equinocandinas são promissores para uso no tratamento de pacientes com aspergilose refratária ao tratamento padrão; diferentes perfis de suscetilidade de Aspergillus a antifúngicos testados isoladamente e em associação podem ser encontrados dependendo da metodologia utilizada, fazendo-se necessária a padronização dos diferentes testes na busca de metodologias mais fáceis e rápidas que facilitem seu uso em laboratórios de rotina. Finalmente, o primeiro relato da presença de mecanismos de resistência a azólicos ligadas ao gene cyp51A em isolados brasileiros de Aspergillus gera preocupação com o gerenciamento das aspergiloses nos centros clínicos do Brasil a fim de evitar que as taxas de resistência elevem-se pelo uso indiscriminado de azólicos na clínica e na agricultura.Universidade Federal de Santa MariaBrasilFarmacologiaUFSMPrograma de Pós-Graduação em Ciências FarmacêuticasCentro de Ciências da SaúdeAlves, Sydney Hartzhttp://lattes.cnpq.br/0330782478769631Fuentefria, Alexandre Meneghellohttp://lattes.cnpq.br/3011308324416888Verweij, Paul Eduardhttps://publons.com/researcher/1419486/pe-verweij/Santurio, Janio Moraishttp://lattes.cnpq.br/6316012260769979Pereira, Daniela Isabel Brayerhttp://lattes.cnpq.br/3382450720179401Denardi, Laura Bedin2021-03-26T10:26:00Z2021-03-26T10:26:00Z2018-01-19info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfhttp://repositorio.ufsm.br/handle/1/20458ark:/26339/0013000000qt9porAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2021-09-24T17:30:38Zoai:repositorio.ufsm.br:1/20458Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2021-09-24T17:30:38Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Aspergillus spp.: suscetibilidade aos antifúngicos isolados e em associação por diferentes metodologias e detecção de mecanismos de resistência a azólicos
Aspergillus spp.: susceptibility to antifungal drugs alone and in combination using different methodologies and detection of azole resistance mechanisms
title Aspergillus spp.: suscetibilidade aos antifúngicos isolados e em associação por diferentes metodologias e detecção de mecanismos de resistência a azólicos
spellingShingle Aspergillus spp.: suscetibilidade aos antifúngicos isolados e em associação por diferentes metodologias e detecção de mecanismos de resistência a azólicos
Denardi, Laura Bedin
Aspergillus spp.
Resistência a azólicos
Interações entre antifúngicos
Aspergilosis
Azole Resistance
Antifungal interactions
Aspergillosis
CNPQ::CIENCIAS DA SAUDE::FARMACIA
title_short Aspergillus spp.: suscetibilidade aos antifúngicos isolados e em associação por diferentes metodologias e detecção de mecanismos de resistência a azólicos
title_full Aspergillus spp.: suscetibilidade aos antifúngicos isolados e em associação por diferentes metodologias e detecção de mecanismos de resistência a azólicos
title_fullStr Aspergillus spp.: suscetibilidade aos antifúngicos isolados e em associação por diferentes metodologias e detecção de mecanismos de resistência a azólicos
title_full_unstemmed Aspergillus spp.: suscetibilidade aos antifúngicos isolados e em associação por diferentes metodologias e detecção de mecanismos de resistência a azólicos
title_sort Aspergillus spp.: suscetibilidade aos antifúngicos isolados e em associação por diferentes metodologias e detecção de mecanismos de resistência a azólicos
author Denardi, Laura Bedin
author_facet Denardi, Laura Bedin
author_role author
dc.contributor.none.fl_str_mv Alves, Sydney Hartz
http://lattes.cnpq.br/0330782478769631
Fuentefria, Alexandre Meneghello
http://lattes.cnpq.br/3011308324416888
Verweij, Paul Eduard
https://publons.com/researcher/1419486/pe-verweij/
Santurio, Janio Morais
http://lattes.cnpq.br/6316012260769979
Pereira, Daniela Isabel Brayer
http://lattes.cnpq.br/3382450720179401
dc.contributor.author.fl_str_mv Denardi, Laura Bedin
dc.subject.por.fl_str_mv Aspergillus spp.
Resistência a azólicos
Interações entre antifúngicos
Aspergilosis
Azole Resistance
Antifungal interactions
Aspergillosis
CNPQ::CIENCIAS DA SAUDE::FARMACIA
topic Aspergillus spp.
Resistência a azólicos
Interações entre antifúngicos
Aspergilosis
Azole Resistance
Antifungal interactions
Aspergillosis
CNPQ::CIENCIAS DA SAUDE::FARMACIA
description Aspergillosis is a group of diseases among the main causes of morbidity and mortality in immunosuppressed patients. Aspergillus fumigatus is the most common species that causes invasive and non-invasive aspergillosis in humans, followed by Aspergillus flavus, Aspergillus niger and Aspergillus terreus. Azole antifungals are the main treatment of these infections, with voriconazole being the drug of choice in invasive aspergillosis. Echinocandins and amphotericin B are also active against Aspergillus and are currently used in specific situations or in association with azoles. Azole resistance has been increasingly documented among medical centers around the world, mainly associated with A. fumigatus, and has become a major therapeutic problem. The development of resistance has been associated with mutations in the cyp51A gene of A. fumigatus. Two pathways of resistance selection have been studied, the pathway in the patient, and more recently, an environmental route. In order to overcome resistance, alternatives such as the use of combination drugs have been studied in the treatment of patients with aspergillosis refractory to standard treatment. This study aimed to determine the susceptibility profile of A. fumigatus and A. flavus, isolated from patients with aspergillosis or from the environment against azole antifungals, echinocandins and amphotericin B, alone and in combination, by using different methodologies. In addition, resistance mechanisms of clinical or environmental strains of A. fumigatus that showed resistance to one or more azole antifungals were investigated. The main results showed that in either environmental or clinical strains some azole resistant profiles were detected, while the echinocandins were very active against both species of Aspergillus. Amphotericin B showed more pronounced activity against A. fumigatus in comparison to A. flavus. In addition, Etest and agar plates with azole methodologies have been found to be capable of determining the minimum inhibitory concentration (MIC) and detecting resistance of A. fumigatus to isavuconazole, respectively, in accordance with the standard broth microdilution method. The interactions between azole and echinocandin antifungal agents against A. fumigatus varied depending on the methodology used, making it very important to standardize these methods to obtain concordant results. However, the synergistic interactions found in vitro and in vivo showed a favorable effect to the use of these associations in the treatment of aspergillosis. In the azole-echinocandin combinations against A. flavus, a higher percentage of synergistic interactions were observed when the MIC was read while by reading the minimum effective concentration (MEC) indifference was the main outcome. Furthermore, mutations linked to the cyp51A gene were found in one clinical and one environmental itraconazole-resistant A. fumigatus strains. In conclusion, combinations between azoles and echinocandins are promising for use in the treatment of patients with aspergillosis refractory to standard treatment; different Aspergillus susceptibility profiles to antifungals tested alone and in association can be found depending on the methodology used, making it necessary to standardize the different tests in order to have easier and faster methodologies that facilitate their use in routine laboratories. Finally, the first report of the presence of mechanisms of resistance to azoles linked to the cyp51A gene in Brazilian Aspergillus isolates generates concern with the management of aspergillosis in clinical centers of Brazil in order to avoid that the resistance rates increase by the indiscriminate use of azoles in the clinic and in agriculture.
publishDate 2018
dc.date.none.fl_str_mv 2018-01-19
2021-03-26T10:26:00Z
2021-03-26T10:26:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://repositorio.ufsm.br/handle/1/20458
dc.identifier.dark.fl_str_mv ark:/26339/0013000000qt9
url http://repositorio.ufsm.br/handle/1/20458
identifier_str_mv ark:/26339/0013000000qt9
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Farmacologia
UFSM
Programa de Pós-Graduação em Ciências Farmacêuticas
Centro de Ciências da Saúde
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Farmacologia
UFSM
Programa de Pós-Graduação em Ciências Farmacêuticas
Centro de Ciências da Saúde
dc.source.none.fl_str_mv reponame:Manancial - Repositório Digital da UFSM
instname:Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
instname_str Universidade Federal de Santa Maria (UFSM)
instacron_str UFSM
institution UFSM
reponame_str Manancial - Repositório Digital da UFSM
collection Manancial - Repositório Digital da UFSM
repository.name.fl_str_mv Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv atendimento.sib@ufsm.br||tedebc@gmail.com
_version_ 1815172259495542784