Anti-Candida and anti-Cryptococcus evaluation of 15 non-alkaloidal compounds from Pterogyne nitens

Objective: To evaluate anti-Candida and anti-Cryptococcus activities of 15 non-alkaloidal compounds from Pterogyne nitens Tulasne (Leguminosae), a South American medicinal plant. Methods: Compounds were submitted to antifungal assays, using microdilution method described by Clinical and Laboratory S...

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Main Authors: Caroline Sprengel Lima, Carlos Roberto Polaquini, Mariana Bastos dos Santos, Fernanda Patrícia Gullo, Fernanda Sangalli Leite, Liliane Scorzoni, Vanderlan da Silva Bolzani, Maria José Soares Mendes-Giannini, Ana Marisa Fusco-Almeida, Andréia Alves Rezende, Luis Octavio Regasini
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-10-01
Series:Asian Pacific Journal of Tropical Biomedicine
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2221169115309655
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author Caroline Sprengel Lima
Carlos Roberto Polaquini
Mariana Bastos dos Santos
Fernanda Patrícia Gullo
Fernanda Sangalli Leite
Liliane Scorzoni
Vanderlan da Silva Bolzani
Maria José Soares Mendes-Giannini
Ana Marisa Fusco-Almeida
Andréia Alves Rezende
Luis Octavio Regasini
author_facet Caroline Sprengel Lima
Carlos Roberto Polaquini
Mariana Bastos dos Santos
Fernanda Patrícia Gullo
Fernanda Sangalli Leite
Liliane Scorzoni
Vanderlan da Silva Bolzani
Maria José Soares Mendes-Giannini
Ana Marisa Fusco-Almeida
Andréia Alves Rezende
Luis Octavio Regasini
author_sort Caroline Sprengel Lima
collection DOAJ
description Objective: To evaluate anti-Candida and anti-Cryptococcus activities of 15 non-alkaloidal compounds from Pterogyne nitens Tulasne (Leguminosae), a South American medicinal plant. Methods: Compounds were submitted to antifungal assays, using microdilution method described by Clinical and Laboratory Standards Institute document, with minor modifications. Five species of Candida and two species of Cryptococcus, including clinical isolates were screened. Antifungal activity was expressed by minimum inhibitory concentration (MIC). Amphotericin B and fluconazole were used as standard antifungal drugs. Results: Among tested compounds, six substances presented fungal growth inhibition (MIC < 31.2 μg/mL) [three flavone derivatives (1–3), a glycosylated flavonol derivative (5) and two phenolic acids (10 and 12)]. Sorbifolin (1), exhibited potent antifungal activity, demonstrating MIC value of 3.90 μg/mL against Candida glabrata ATCC 90030, Cryptococcus gattii 118 and fluconazole-resistant clinical isolate of Cryptococcus neoformans var. grubii. Pedalin (2) and nitensoside B (3), two glycosylated flavone derivatives, were active against Cryptococcus neoformans ATCC 90012 (MIC = 7.80 μg/mL). Conclusions: Flavone derivatives from Pterogyne nitens can serve as prototypes for the design and development of innovative anti-Candida and anti-Cryptococcus hits.
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spelling doaj.art-1359685ecffb451b886251f68476809c2022-12-22T00:04:42ZengWolters Kluwer Medknow PublicationsAsian Pacific Journal of Tropical Biomedicine2221-16912016-10-0161084184510.1016/j.apjtb.2016.08.003Anti-Candida and anti-Cryptococcus evaluation of 15 non-alkaloidal compounds from Pterogyne nitensCaroline Sprengel Lima0Carlos Roberto Polaquini1Mariana Bastos dos Santos2Fernanda Patrícia Gullo3Fernanda Sangalli Leite4Liliane Scorzoni5Vanderlan da Silva Bolzani6Maria José Soares Mendes-Giannini7Ana Marisa Fusco-Almeida8Andréia Alves Rezende9Luis Octavio Regasini10Laboratory of Green and Medicinal Chemistry, Department of Chemistry and Environmental Sciences, Institute of Biosciences, Letters and Exact Sciences, São Paulo State University (UNESP), São José do Rio Preto, Sao Paulo, BrazilLaboratory of Green and Medicinal Chemistry, Department of Chemistry and Environmental Sciences, Institute of Biosciences, Letters and Exact Sciences, São Paulo State University (UNESP), São José do Rio Preto, Sao Paulo, BrazilLaboratory of Green and Medicinal Chemistry, Department of Chemistry and Environmental Sciences, Institute of Biosciences, Letters and Exact Sciences, São Paulo State University (UNESP), São José do Rio Preto, Sao Paulo, BrazilDepartment of Clinical Analysis, School of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo, BrazilDepartment of Clinical Analysis, School of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo, BrazilDepartment of Clinical Analysis, School of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo, BrazilDepartment of Organic Chemistry, Institute of Chemistry, São Paulo State University (UNESP), Araraquara, São Paulo, BrazilDepartment of Clinical Analysis, School of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo, BrazilDepartment of Clinical Analysis, School of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo, BrazilDepartment of Biology and Animal Sciences, Faculty of Engineering, São Paulo State University (UNESP), Ilha Solteira, São Paulo, BrazilLaboratory of Green and Medicinal Chemistry, Department of Chemistry and Environmental Sciences, Institute of Biosciences, Letters and Exact Sciences, São Paulo State University (UNESP), São José do Rio Preto, Sao Paulo, BrazilObjective: To evaluate anti-Candida and anti-Cryptococcus activities of 15 non-alkaloidal compounds from Pterogyne nitens Tulasne (Leguminosae), a South American medicinal plant. Methods: Compounds were submitted to antifungal assays, using microdilution method described by Clinical and Laboratory Standards Institute document, with minor modifications. Five species of Candida and two species of Cryptococcus, including clinical isolates were screened. Antifungal activity was expressed by minimum inhibitory concentration (MIC). Amphotericin B and fluconazole were used as standard antifungal drugs. Results: Among tested compounds, six substances presented fungal growth inhibition (MIC < 31.2 μg/mL) [three flavone derivatives (1–3), a glycosylated flavonol derivative (5) and two phenolic acids (10 and 12)]. Sorbifolin (1), exhibited potent antifungal activity, demonstrating MIC value of 3.90 μg/mL against Candida glabrata ATCC 90030, Cryptococcus gattii 118 and fluconazole-resistant clinical isolate of Cryptococcus neoformans var. grubii. Pedalin (2) and nitensoside B (3), two glycosylated flavone derivatives, were active against Cryptococcus neoformans ATCC 90012 (MIC = 7.80 μg/mL). Conclusions: Flavone derivatives from Pterogyne nitens can serve as prototypes for the design and development of innovative anti-Candida and anti-Cryptococcus hits.http://www.sciencedirect.com/science/article/pii/S2221169115309655CandidaCryptococcusAntifungalPterogyne nitensFlavonoidOpportunistic fungi
spellingShingle Caroline Sprengel Lima
Carlos Roberto Polaquini
Mariana Bastos dos Santos
Fernanda Patrícia Gullo
Fernanda Sangalli Leite
Liliane Scorzoni
Vanderlan da Silva Bolzani
Maria José Soares Mendes-Giannini
Ana Marisa Fusco-Almeida
Andréia Alves Rezende
Luis Octavio Regasini
Anti-Candida and anti-Cryptococcus evaluation of 15 non-alkaloidal compounds from Pterogyne nitens
Asian Pacific Journal of Tropical Biomedicine
Candida
Cryptococcus
Antifungal
Pterogyne nitens
Flavonoid
Opportunistic fungi
title Anti-Candida and anti-Cryptococcus evaluation of 15 non-alkaloidal compounds from Pterogyne nitens
title_full Anti-Candida and anti-Cryptococcus evaluation of 15 non-alkaloidal compounds from Pterogyne nitens
title_fullStr Anti-Candida and anti-Cryptococcus evaluation of 15 non-alkaloidal compounds from Pterogyne nitens
title_full_unstemmed Anti-Candida and anti-Cryptococcus evaluation of 15 non-alkaloidal compounds from Pterogyne nitens
title_short Anti-Candida and anti-Cryptococcus evaluation of 15 non-alkaloidal compounds from Pterogyne nitens
title_sort anti candida and anti cryptococcus evaluation of 15 non alkaloidal compounds from pterogyne nitens
topic Candida
Cryptococcus
Antifungal
Pterogyne nitens
Flavonoid
Opportunistic fungi
url http://www.sciencedirect.com/science/article/pii/S2221169115309655
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