Molecular Diagnosis Compared to Conventional Diagnosis for Rapid Detection of Resistant Strains of Candida Spp.
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Research, Society and Development |
Texto Completo: | https://rsdjournal.org/index.php/rsd/article/view/41088 |
Resumo: | Yeast Candida spp. can cause serious infections, especially in patients of the hospital environment. Variation in the virulence profile of Candida clinical isolates and high mortality rates indicate the importance of rapid and accurate identification, as well as susceptibility testing for successful candidiasis treatment. A total of 20 strains were isolated from patients from Tertiary Hospital of the Northern Zone of Ceará. PCR amplification followed by agarose gel electrophoresis (PCR-AGE) and the manual method (culturing on CHROMagar-Candida) and VITEK automated method were used to test a total of 20 fungal strains from clinics sources. Five strains of C. albicans, 2 of C. tropicalis and 4 strains of C. parapsilosis which were cultured for the determination of MIC (Minimum Inhibitory Concentration). The best sensitivity rate was demonstrated by automatic identification and PCR-AGE, where all 20 strains isolated with a sensitivity profile of 100% (20/20) were completely identified. According to the data obtained, resistance to amphotericin B (CIM ≥ 1 µg/ml) was observed in some isolates of C. tropicalis and C. parapsilosis. However, for the other antifungals, these same species presented 100% sensitivity (MIC ≤ 0.125 μg / ml; MIC ≤ 8 μg / ml). Isolates of C. albicans were sensitive to all antifungal agents with 100% sensitivity, although 75% of the isolates showed a tendency for less susceptibility to amphotericin B. In this study, we confirmed the efficacy and applicability of PCR-AGE in the identification and differentiation of yeast Candida spp. from clinical samples. |
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Molecular Diagnosis Compared to Conventional Diagnosis for Rapid Detection of Resistant Strains of Candida Spp.Diagnóstico Molecular Comparado con el Diagnóstico Convencional para la Detección Rápida de Cepas Resistentes de Candida Spp.Diagnóstico Molecular Comparado ao Diagnóstico Convencional para Detecção Rápida de Cepas Resistentes de Candida Spp.Candida SppMolecular identificationAntifungal activity.Candida SppIdentificación molecularActividad antifúngica.Candida SppIdentificação molecularAtividade antifúngica.Yeast Candida spp. can cause serious infections, especially in patients of the hospital environment. Variation in the virulence profile of Candida clinical isolates and high mortality rates indicate the importance of rapid and accurate identification, as well as susceptibility testing for successful candidiasis treatment. A total of 20 strains were isolated from patients from Tertiary Hospital of the Northern Zone of Ceará. PCR amplification followed by agarose gel electrophoresis (PCR-AGE) and the manual method (culturing on CHROMagar-Candida) and VITEK automated method were used to test a total of 20 fungal strains from clinics sources. Five strains of C. albicans, 2 of C. tropicalis and 4 strains of C. parapsilosis which were cultured for the determination of MIC (Minimum Inhibitory Concentration). The best sensitivity rate was demonstrated by automatic identification and PCR-AGE, where all 20 strains isolated with a sensitivity profile of 100% (20/20) were completely identified. According to the data obtained, resistance to amphotericin B (CIM ≥ 1 µg/ml) was observed in some isolates of C. tropicalis and C. parapsilosis. However, for the other antifungals, these same species presented 100% sensitivity (MIC ≤ 0.125 μg / ml; MIC ≤ 8 μg / ml). Isolates of C. albicans were sensitive to all antifungal agents with 100% sensitivity, although 75% of the isolates showed a tendency for less susceptibility to amphotericin B. In this study, we confirmed the efficacy and applicability of PCR-AGE in the identification and differentiation of yeast Candida spp. from clinical samples.La levedura Candida spp. pode causar infecciones graves, principalmente em pacientes no ambiente hospitalar. Una variación en el perfil de virulência de dos aislados clínicos de Candida y como altos taxones de mortalidad indica una importancia de su identificación rápida y precisa, como prueba de suscetibilidad para el tratamiento exitoso de la candidiasis. Foi utilizado en un total de 20 cepas foram aisladas de pacientes del Hospital Terciário da Zona Norte do Ceará. Una amplificación por PCR seguida de electroforesis en gel de agarosa (PCR-AGE) y un método manual (cultivo en CHROMagar-Candida) y un método automatizado VITEK para probar un total de 20 cepas fúngicas de fuentes clínicas. Cinco cepas de C. albicans, dos de C. tropicalis y cuatro cepas de C. parapsilosis que foram cultivadas para determinación de CIM (Concentração Inibitória Mínima). Una mejor taxa de sensibilidad foi demostrada pela identificação automática e PCR-AGE, una vez que 20 cepas aisladas con perfil de sensibilidad de 100% (20/20) foram totalmente identificadas. De acuerdo con los dados obtenidos, la resistencia a la anfotericina B (CIM ≥ 1 µg/ml) se observó en algunos aislados de C. tropicalis y C. parapsilosis. Entretanto, para os demais antifúngicos, essas mesmas espécies apresentaram 100% de sensibilidade (CIM ≤ 0,125 μg/ml; CIM ≤ 8 μg/ml). Los aislados de C. albicans fueron sensibles a todos los antifúngicos, aunque el 75% de las cepas tendieron a ser menos sensibles a la anfotericina B. Este estudio mostró evidencia sobre la eficacia y aplicabilidad de PCR-AGE en la identificación y diferenciación de Candida spp. de muestras clínicas.A levedura Candida spp. pode causar infecções graves, principalmente em pacientes no ambiente hospitalar. A variação no perfil de virulência dos isolados clínicos de Candida e as altas taxas de mortalidade indicam a importância da sua identificação rápida e precisa, bem como do teste de sensibilidade para o sucesso do tratamento da candidíase. Foi utilizado um total de 20 cepas isoladas de pacientes de um Hospital Terciário da Zona Norte do Ceará. A amplificação por PCR seguida de eletroforese em gel de agarose (PCR-AGE) e o método manual (cultivo em CHROMagar-Candida) e o método automatizado VITEK foram usados para identificar um total de 20 cepas fúngicas oriundas de quadros clínicos diversos. Cinco cepas de C. albicans, duas de C. tropicalis e quatro cepas de C. parapsilosis foram utlizadas para determinação de CIM (Concentração Inibitória Mínima). Os testes que demonstraram maior sensibilidade foram a identificação automática e PCR-AGE, onde todas as 20 cepas testadas apresentaram perfil de sensibilidade de 100% (20/20) apresentando completa identificação. De acordo com os dados obtidos, resistência à anfotericina B (CIM ≥ 1 µg/ml) foi observada em alguns isolados de C. tropicalis e C. parapsilosis. Entretanto, para os demais antifúngicos, essas mesmas espécies apresentaram-se sensíveis (CIM ≤ 0,125 μg/ml; CIM ≤ 8 μg/ml). Os isolados de C. albicans foram sensíveis a todos os antifúngicos, embora 75% das cepas tenham tendência a menor sensibilidade à anfotericina B. Este estudo mostrou evidências a eficácia e aplicabilidade da PCR-AGE na identificação e diferenciação da levedura Candida spp. a partir de amostras clínicas. Research, Society and Development2023-04-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/4108810.33448/rsd-v12i4.41088Research, Society and Development; Vol. 12 No. 4; e14112441088Research, Society and Development; Vol. 12 Núm. 4; e14112441088Research, Society and Development; v. 12 n. 4; e141124410882525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIenghttps://rsdjournal.org/index.php/rsd/article/view/41088/33464Copyright (c) 2023 Rafael Carneiro Bastos; Erivan Ferreira Alves; Andréa Maria Neves; Carlos Franciney Moreira Vasconcelos; Erika Helena Salles de Brito; Raquel Oliveira dos Santos Fontenellehttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessBastos, Rafael Carneiro Alves, Erivan Ferreira Neves, Andréa MariaVasconcelos, Carlos Franciney Moreira Brito, Erika Helena Salles deFontenelle, Raquel Oliveira dos Santos 2023-04-21T18:13:32Zoai:ojs.pkp.sfu.ca:article/41088Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2023-04-21T18:13:32Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false |
dc.title.none.fl_str_mv |
Molecular Diagnosis Compared to Conventional Diagnosis for Rapid Detection of Resistant Strains of Candida Spp. Diagnóstico Molecular Comparado con el Diagnóstico Convencional para la Detección Rápida de Cepas Resistentes de Candida Spp. Diagnóstico Molecular Comparado ao Diagnóstico Convencional para Detecção Rápida de Cepas Resistentes de Candida Spp. |
title |
Molecular Diagnosis Compared to Conventional Diagnosis for Rapid Detection of Resistant Strains of Candida Spp. |
spellingShingle |
Molecular Diagnosis Compared to Conventional Diagnosis for Rapid Detection of Resistant Strains of Candida Spp. Bastos, Rafael Carneiro Candida Spp Molecular identification Antifungal activity. Candida Spp Identificación molecular Actividad antifúngica. Candida Spp Identificação molecular Atividade antifúngica. |
title_short |
Molecular Diagnosis Compared to Conventional Diagnosis for Rapid Detection of Resistant Strains of Candida Spp. |
title_full |
Molecular Diagnosis Compared to Conventional Diagnosis for Rapid Detection of Resistant Strains of Candida Spp. |
title_fullStr |
Molecular Diagnosis Compared to Conventional Diagnosis for Rapid Detection of Resistant Strains of Candida Spp. |
title_full_unstemmed |
Molecular Diagnosis Compared to Conventional Diagnosis for Rapid Detection of Resistant Strains of Candida Spp. |
title_sort |
Molecular Diagnosis Compared to Conventional Diagnosis for Rapid Detection of Resistant Strains of Candida Spp. |
author |
Bastos, Rafael Carneiro |
author_facet |
Bastos, Rafael Carneiro Alves, Erivan Ferreira Neves, Andréa Maria Vasconcelos, Carlos Franciney Moreira Brito, Erika Helena Salles de Fontenelle, Raquel Oliveira dos Santos |
author_role |
author |
author2 |
Alves, Erivan Ferreira Neves, Andréa Maria Vasconcelos, Carlos Franciney Moreira Brito, Erika Helena Salles de Fontenelle, Raquel Oliveira dos Santos |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Bastos, Rafael Carneiro Alves, Erivan Ferreira Neves, Andréa Maria Vasconcelos, Carlos Franciney Moreira Brito, Erika Helena Salles de Fontenelle, Raquel Oliveira dos Santos |
dc.subject.por.fl_str_mv |
Candida Spp Molecular identification Antifungal activity. Candida Spp Identificación molecular Actividad antifúngica. Candida Spp Identificação molecular Atividade antifúngica. |
topic |
Candida Spp Molecular identification Antifungal activity. Candida Spp Identificación molecular Actividad antifúngica. Candida Spp Identificação molecular Atividade antifúngica. |
description |
Yeast Candida spp. can cause serious infections, especially in patients of the hospital environment. Variation in the virulence profile of Candida clinical isolates and high mortality rates indicate the importance of rapid and accurate identification, as well as susceptibility testing for successful candidiasis treatment. A total of 20 strains were isolated from patients from Tertiary Hospital of the Northern Zone of Ceará. PCR amplification followed by agarose gel electrophoresis (PCR-AGE) and the manual method (culturing on CHROMagar-Candida) and VITEK automated method were used to test a total of 20 fungal strains from clinics sources. Five strains of C. albicans, 2 of C. tropicalis and 4 strains of C. parapsilosis which were cultured for the determination of MIC (Minimum Inhibitory Concentration). The best sensitivity rate was demonstrated by automatic identification and PCR-AGE, where all 20 strains isolated with a sensitivity profile of 100% (20/20) were completely identified. According to the data obtained, resistance to amphotericin B (CIM ≥ 1 µg/ml) was observed in some isolates of C. tropicalis and C. parapsilosis. However, for the other antifungals, these same species presented 100% sensitivity (MIC ≤ 0.125 μg / ml; MIC ≤ 8 μg / ml). Isolates of C. albicans were sensitive to all antifungal agents with 100% sensitivity, although 75% of the isolates showed a tendency for less susceptibility to amphotericin B. In this study, we confirmed the efficacy and applicability of PCR-AGE in the identification and differentiation of yeast Candida spp. from clinical samples. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-04-05 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/41088 10.33448/rsd-v12i4.41088 |
url |
https://rsdjournal.org/index.php/rsd/article/view/41088 |
identifier_str_mv |
10.33448/rsd-v12i4.41088 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/41088/33464 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Research, Society and Development |
publisher.none.fl_str_mv |
Research, Society and Development |
dc.source.none.fl_str_mv |
Research, Society and Development; Vol. 12 No. 4; e14112441088 Research, Society and Development; Vol. 12 Núm. 4; e14112441088 Research, Society and Development; v. 12 n. 4; e14112441088 2525-3409 reponame:Research, Society and Development instname:Universidade Federal de Itajubá (UNIFEI) instacron:UNIFEI |
instname_str |
Universidade Federal de Itajubá (UNIFEI) |
instacron_str |
UNIFEI |
institution |
UNIFEI |
reponame_str |
Research, Society and Development |
collection |
Research, Society and Development |
repository.name.fl_str_mv |
Research, Society and Development - Universidade Federal de Itajubá (UNIFEI) |
repository.mail.fl_str_mv |
rsd.articles@gmail.com |
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1797052622085029888 |