In vitro antibiotic and modulatory activity of Mesosphaerum suaveolens (L.) kuntze against candida strains

Detalhes bibliográficos
Autor(a) principal: Costa, Adrielle Rodrigues
Data de Publicação: 2020
Outros Autores: Bezerra, José Weverton Almeida, Cruz, Rafael Pereira da, Freitas, Maria Audilene de, Silva, Viviane Bezerra da, Neto, João Cruz, dos Santos, Antônia Thassya Lucas, Braga, Maria Flaviana Bezerra Morais, Silva, Leomara Andrade da, Rocha, Maria Ivaneide, Kamdem, J. P., Iriti, Marcello, Vitalini, Sara, Duarte, Antônia Eliene, Barros, Luiz Marivando
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional do INPA
Texto Completo: https://repositorio.inpa.gov.br/handle/1/15458
Resumo: The emergence of fungal resistance to commercial drugs has been a major problem for the WHO. In this context, research with natural products is promising in the discovery of new active substances. Thus, this work evaluated the antifungal effect of a medicinal plant (i.e., Mesosphaerum suaveolens) against strains of the genus Candida, tested the combined effect with the drug fluconazole, and, finally, determined the phenolic constituents present in the species. Initially, aqueous extracts of leaves (AELMs) and aerial parts (AEAPMs) of the species were prepared. For microbiological assays, the minimum fungicidal concentration was determined by broth microdilution, and the combined effect of fluconazole extracts were verified by sub‐inhibitory microdilution concentrations (CFM/8) followed by spectrophotometric readings which were used to determine the IC50. HPLC detected the presence of flavonoids and phenolic acids, detecting eight compounds present in the samples of which caffeic acid and quercetin were major components. The AELMs modulated fluconazole activity since it decreased fluconazole’s IC50 from 7.8 μg/mL to an IC50 of 4.7 μg/mL (CA LM 77) and from 28.8 μg/mL to 18.26 μg/mL (CA INCQS 40006) for the C. albicans strains. The AEAPMs were able to potentiate the effect of fluconazole more effectively than the AELMs. Such an effect was significant for the 16 μg/mL concentration for CA LM 77 and 32 μg/mL for CA INCQS 40006. The AEAPMs as well as the AELMs presented clinically relevant activities for C. tropicalis strains. For the C. tropicalis LM 23 strain, the AEPMs obtained an IC50 of 25 μg/mL and the AELMs an IC50 of 359.9 μg/mL. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
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spelling Costa, Adrielle RodriguesBezerra, José Weverton AlmeidaCruz, Rafael Pereira daFreitas, Maria Audilene deSilva, Viviane Bezerra daNeto, João Cruzdos Santos, Antônia Thassya LucasBraga, Maria Flaviana Bezerra MoraisSilva, Leomara Andrade daRocha, Maria IvaneideKamdem, J. P.Iriti, MarcelloVitalini, SaraDuarte, Antônia ElieneBarros, Luiz Marivando2020-05-14T14:27:40Z2020-05-14T14:27:40Z2020https://repositorio.inpa.gov.br/handle/1/1545810.3390/antibiotics9020046The emergence of fungal resistance to commercial drugs has been a major problem for the WHO. In this context, research with natural products is promising in the discovery of new active substances. Thus, this work evaluated the antifungal effect of a medicinal plant (i.e., Mesosphaerum suaveolens) against strains of the genus Candida, tested the combined effect with the drug fluconazole, and, finally, determined the phenolic constituents present in the species. Initially, aqueous extracts of leaves (AELMs) and aerial parts (AEAPMs) of the species were prepared. For microbiological assays, the minimum fungicidal concentration was determined by broth microdilution, and the combined effect of fluconazole extracts were verified by sub‐inhibitory microdilution concentrations (CFM/8) followed by spectrophotometric readings which were used to determine the IC50. HPLC detected the presence of flavonoids and phenolic acids, detecting eight compounds present in the samples of which caffeic acid and quercetin were major components. The AELMs modulated fluconazole activity since it decreased fluconazole’s IC50 from 7.8 μg/mL to an IC50 of 4.7 μg/mL (CA LM 77) and from 28.8 μg/mL to 18.26 μg/mL (CA INCQS 40006) for the C. albicans strains. The AEAPMs were able to potentiate the effect of fluconazole more effectively than the AELMs. Such an effect was significant for the 16 μg/mL concentration for CA LM 77 and 32 μg/mL for CA INCQS 40006. The AEAPMs as well as the AELMs presented clinically relevant activities for C. tropicalis strains. For the C. tropicalis LM 23 strain, the AEPMs obtained an IC50 of 25 μg/mL and the AELMs an IC50 of 359.9 μg/mL. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.Volume 9, Número 2Attribution-NonCommercial-NoDerivs 3.0 Brazilhttp://creativecommons.org/licenses/by-nc-nd/3.0/br/info:eu-repo/semantics/openAccessAntibiotic AgentApigeninCaffeic AcidCatechinChlorogenic AcidEllagic AcidFlavonoidFluconazoleGallic AcidMesosphaerum Suaveolens ExtractPhenol DerivativePhytochemicalPlant ExtractQuercetinRutosideUnclassified DrugAnti-fungal ActivityAntifungal ResistanceAnti-microbial ActivityBroth DilutionCandidaCandida TropicalisCell ViabilityCell Viability AssayControlled StudyDisk DiffusionDrug ActivityEnzyme-linked Immunosorbent AssayFungal StrainFungus GrowthHigh Performance Liquid ChromatographyIc 50Medicinal PlantMesosphaerum SuaveolensMicrobiologyMinimum Fungicidal ConcentrationMinimum Inhibitory ConcentrationNonhumanPhytochemistryPriority JournalRetention Time (chromatography)SpectrophotometryUltraviolet SpectroscopyIn vitro antibiotic and modulatory activity of Mesosphaerum suaveolens (L.) kuntze against candida strainsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleAntibioticsengreponame:Repositório Institucional do INPAinstname:Instituto Nacional de Pesquisas da Amazônia (INPA)instacron:INPAORIGINALartigo-inpa.pdfartigo-inpa.pdfapplication/pdf3270521https://repositorio.inpa.gov.br/bitstream/1/15458/1/artigo-inpa.pdf96f704028a882e830881fb259809f49bMD511/154582020-05-14 10:58:43.577oai:repositorio:1/15458Repositório de PublicaçõesPUBhttps://repositorio.inpa.gov.br/oai/requestopendoar:2020-05-14T14:58:43Repositório Institucional do INPA - Instituto Nacional de Pesquisas da Amazônia (INPA)false
dc.title.en.fl_str_mv In vitro antibiotic and modulatory activity of Mesosphaerum suaveolens (L.) kuntze against candida strains
title In vitro antibiotic and modulatory activity of Mesosphaerum suaveolens (L.) kuntze against candida strains
spellingShingle In vitro antibiotic and modulatory activity of Mesosphaerum suaveolens (L.) kuntze against candida strains
Costa, Adrielle Rodrigues
Antibiotic Agent
Apigenin
Caffeic Acid
Catechin
Chlorogenic Acid
Ellagic Acid
Flavonoid
Fluconazole
Gallic Acid
Mesosphaerum Suaveolens Extract
Phenol Derivative
Phytochemical
Plant Extract
Quercetin
Rutoside
Unclassified Drug
Anti-fungal Activity
Antifungal Resistance
Anti-microbial Activity
Broth Dilution
Candida
Candida Tropicalis
Cell Viability
Cell Viability Assay
Controlled Study
Disk Diffusion
Drug Activity
Enzyme-linked Immunosorbent Assay
Fungal Strain
Fungus Growth
High Performance Liquid Chromatography
Ic 50
Medicinal Plant
Mesosphaerum Suaveolens
Microbiology
Minimum Fungicidal Concentration
Minimum Inhibitory Concentration
Nonhuman
Phytochemistry
Priority Journal
Retention Time (chromatography)
Spectrophotometry
Ultraviolet Spectroscopy
title_short In vitro antibiotic and modulatory activity of Mesosphaerum suaveolens (L.) kuntze against candida strains
title_full In vitro antibiotic and modulatory activity of Mesosphaerum suaveolens (L.) kuntze against candida strains
title_fullStr In vitro antibiotic and modulatory activity of Mesosphaerum suaveolens (L.) kuntze against candida strains
title_full_unstemmed In vitro antibiotic and modulatory activity of Mesosphaerum suaveolens (L.) kuntze against candida strains
title_sort In vitro antibiotic and modulatory activity of Mesosphaerum suaveolens (L.) kuntze against candida strains
author Costa, Adrielle Rodrigues
author_facet Costa, Adrielle Rodrigues
Bezerra, José Weverton Almeida
Cruz, Rafael Pereira da
Freitas, Maria Audilene de
Silva, Viviane Bezerra da
Neto, João Cruz
dos Santos, Antônia Thassya Lucas
Braga, Maria Flaviana Bezerra Morais
Silva, Leomara Andrade da
Rocha, Maria Ivaneide
Kamdem, J. P.
Iriti, Marcello
Vitalini, Sara
Duarte, Antônia Eliene
Barros, Luiz Marivando
author_role author
author2 Bezerra, José Weverton Almeida
Cruz, Rafael Pereira da
Freitas, Maria Audilene de
Silva, Viviane Bezerra da
Neto, João Cruz
dos Santos, Antônia Thassya Lucas
Braga, Maria Flaviana Bezerra Morais
Silva, Leomara Andrade da
Rocha, Maria Ivaneide
Kamdem, J. P.
Iriti, Marcello
Vitalini, Sara
Duarte, Antônia Eliene
Barros, Luiz Marivando
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Costa, Adrielle Rodrigues
Bezerra, José Weverton Almeida
Cruz, Rafael Pereira da
Freitas, Maria Audilene de
Silva, Viviane Bezerra da
Neto, João Cruz
dos Santos, Antônia Thassya Lucas
Braga, Maria Flaviana Bezerra Morais
Silva, Leomara Andrade da
Rocha, Maria Ivaneide
Kamdem, J. P.
Iriti, Marcello
Vitalini, Sara
Duarte, Antônia Eliene
Barros, Luiz Marivando
dc.subject.eng.fl_str_mv Antibiotic Agent
Apigenin
Caffeic Acid
Catechin
Chlorogenic Acid
Ellagic Acid
Flavonoid
Fluconazole
Gallic Acid
Mesosphaerum Suaveolens Extract
Phenol Derivative
Phytochemical
Plant Extract
Quercetin
Rutoside
Unclassified Drug
Anti-fungal Activity
Antifungal Resistance
Anti-microbial Activity
Broth Dilution
Candida
Candida Tropicalis
Cell Viability
Cell Viability Assay
Controlled Study
Disk Diffusion
Drug Activity
Enzyme-linked Immunosorbent Assay
Fungal Strain
Fungus Growth
High Performance Liquid Chromatography
Ic 50
Medicinal Plant
Mesosphaerum Suaveolens
Microbiology
Minimum Fungicidal Concentration
Minimum Inhibitory Concentration
Nonhuman
Phytochemistry
Priority Journal
Retention Time (chromatography)
Spectrophotometry
Ultraviolet Spectroscopy
topic Antibiotic Agent
Apigenin
Caffeic Acid
Catechin
Chlorogenic Acid
Ellagic Acid
Flavonoid
Fluconazole
Gallic Acid
Mesosphaerum Suaveolens Extract
Phenol Derivative
Phytochemical
Plant Extract
Quercetin
Rutoside
Unclassified Drug
Anti-fungal Activity
Antifungal Resistance
Anti-microbial Activity
Broth Dilution
Candida
Candida Tropicalis
Cell Viability
Cell Viability Assay
Controlled Study
Disk Diffusion
Drug Activity
Enzyme-linked Immunosorbent Assay
Fungal Strain
Fungus Growth
High Performance Liquid Chromatography
Ic 50
Medicinal Plant
Mesosphaerum Suaveolens
Microbiology
Minimum Fungicidal Concentration
Minimum Inhibitory Concentration
Nonhuman
Phytochemistry
Priority Journal
Retention Time (chromatography)
Spectrophotometry
Ultraviolet Spectroscopy
description The emergence of fungal resistance to commercial drugs has been a major problem for the WHO. In this context, research with natural products is promising in the discovery of new active substances. Thus, this work evaluated the antifungal effect of a medicinal plant (i.e., Mesosphaerum suaveolens) against strains of the genus Candida, tested the combined effect with the drug fluconazole, and, finally, determined the phenolic constituents present in the species. Initially, aqueous extracts of leaves (AELMs) and aerial parts (AEAPMs) of the species were prepared. For microbiological assays, the minimum fungicidal concentration was determined by broth microdilution, and the combined effect of fluconazole extracts were verified by sub‐inhibitory microdilution concentrations (CFM/8) followed by spectrophotometric readings which were used to determine the IC50. HPLC detected the presence of flavonoids and phenolic acids, detecting eight compounds present in the samples of which caffeic acid and quercetin were major components. The AELMs modulated fluconazole activity since it decreased fluconazole’s IC50 from 7.8 μg/mL to an IC50 of 4.7 μg/mL (CA LM 77) and from 28.8 μg/mL to 18.26 μg/mL (CA INCQS 40006) for the C. albicans strains. The AEAPMs were able to potentiate the effect of fluconazole more effectively than the AELMs. Such an effect was significant for the 16 μg/mL concentration for CA LM 77 and 32 μg/mL for CA INCQS 40006. The AEAPMs as well as the AELMs presented clinically relevant activities for C. tropicalis strains. For the C. tropicalis LM 23 strain, the AEPMs obtained an IC50 of 25 μg/mL and the AELMs an IC50 of 359.9 μg/mL. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
publishDate 2020
dc.date.accessioned.fl_str_mv 2020-05-14T14:27:40Z
dc.date.available.fl_str_mv 2020-05-14T14:27:40Z
dc.date.issued.fl_str_mv 2020
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://repositorio.inpa.gov.br/handle/1/15458
dc.identifier.doi.none.fl_str_mv 10.3390/antibiotics9020046
url https://repositorio.inpa.gov.br/handle/1/15458
identifier_str_mv 10.3390/antibiotics9020046
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Volume 9, Número 2
dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivs 3.0 Brazil
http://creativecommons.org/licenses/by-nc-nd/3.0/br/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivs 3.0 Brazil
http://creativecommons.org/licenses/by-nc-nd/3.0/br/
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Antibiotics
publisher.none.fl_str_mv Antibiotics
dc.source.none.fl_str_mv reponame:Repositório Institucional do INPA
instname:Instituto Nacional de Pesquisas da Amazônia (INPA)
instacron:INPA
instname_str Instituto Nacional de Pesquisas da Amazônia (INPA)
instacron_str INPA
institution INPA
reponame_str Repositório Institucional do INPA
collection Repositório Institucional do INPA
bitstream.url.fl_str_mv https://repositorio.inpa.gov.br/bitstream/1/15458/1/artigo-inpa.pdf
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repository.name.fl_str_mv Repositório Institucional do INPA - Instituto Nacional de Pesquisas da Amazônia (INPA)
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