Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
Plant Biol (Stuttg) ; 19(4): 599-607, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-28403565

RESUMO

Pseudomonas syringae is a phytopathogenic bacterium that causes lesions in leaves during the colonisation process. The damage is associated with production of many virulence factors, such as biofilm and phytotoxins. The essential oils of Thymus vulgaris (thyme) and Origanum vulgare (oregano) have been demonstrated to inhibit P. syringae. The aim of this study was to investigate the effects of T. vulgaris and O. vulgare essential oils on production of virulence factors of phytopathogenic P. syringae strains, including anti-biofilm and anti-toxins activities. The broth microdilution method was used for determination of MIC and biofilm inhibition assays. Coronatine, syringomycin and tabtoxin were pheno- and genotypically evaluated. Both oils showed good inhibitory activity against P. syringae, with MIC values from 1.43 to 11.5 mg·ml-1 for thyme and 5.8 to 11.6 mg·ml-1 for oregano. Biofilm formation, production of coronatine, syringomycin and tabtoxin were inhibited by thyme and oregano essential oil in most strains. The results presented here are promising, demonstrating the bactericidal activity and reduction of virulence factor production after treatment with thyme and oregano oil, providing insight into how they exert their antibacterial activity. These natural products could be considered in the future for the control of diseases caused by P. syringae.


Assuntos
Óleos Voláteis/química , Óleos Voláteis/farmacologia , Origanum/química , Extratos Vegetais/farmacologia , Pseudomonas syringae/efeitos dos fármacos , Pseudomonas syringae/metabolismo , Thymus (Planta)/química , Fatores de Virulência/metabolismo , Aminoácidos/metabolismo , Proteínas de Bactérias/metabolismo , Dipeptídeos/metabolismo , Indenos/metabolismo , Testes de Sensibilidade Microbiana
2.
Plant Biol (Stuttg) ; 17(3): 758-65, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-25359697

RESUMO

The aim of this work was to study the antimicrobial activity of essential oils obtained from Thymus vulgaris (thyme) and Origanum vulgare (oregano) on phytopathogenic Pseudomonas species isolated from soybean. Strains with characteristics of P. syringae were isolated from leaves of soybean plants with blight symptoms. Ten of these could be identified in Group Ia of LOPAT as P. syringae. Six of these were confirmed as P. syringae using 16S rRNA, indicating the presence of these phytopathogenic bacteria in east and central Argentina. All the phytopathogenic bacteria were re-isolated and identified from the infected plants. MIC values for thyme were 11.5 and 5.7 mg·ml(-1) on P. syringae strains, while oregano showed variability in the inhibitory activity. Both essential oils inhibited all P. syringae strains, with better inhibitory activity than the antibiotic streptomycin. The oils were not bactericidal for all pseudomonads. Both oils contained high carvacrol (29.5% and 19.7%, respectively) and low thymol (1.5%). Natural products obtained from aromatic plants represent potential sources of molecules with biological activity that could be used as new alternatives for the treatment of phytopathogenic bacteria infections.


Assuntos
Anti-Infecciosos/farmacologia , Glycine max/microbiologia , Óleos Voláteis/farmacologia , Origanum/química , Doenças das Plantas/microbiologia , Pseudomonas syringae/efeitos dos fármacos , Thymus (Planta)/química , Anti-Infecciosos/análise , Argentina , Sequência de Bases , Cimenos , Testes de Sensibilidade Microbiana , Dados de Sequência Molecular , Monoterpenos/análise , Monoterpenos/farmacologia , Óleos Voláteis/química , Extratos Vegetais/química , Extratos Vegetais/farmacologia , Folhas de Planta/microbiologia , Pseudomonas syringae/genética , Pseudomonas syringae/isolamento & purificação , RNA Bacteriano/análise , RNA Ribossômico 16S/análise , Timol/análise , Timol/farmacologia
3.
J Appl Microbiol ; 116(4): 795-804, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24387763

RESUMO

AIMS: To evaluate the antifungal activity and to analyse the structure-activity relationship of eleven natural phenolic compounds against four Candida species which are resistant to fluconazole. METHODS AND RESULTS: Four different species of Candida isolates were used: Candida albicans, Candida krusei, Candida tropicalis and Candida dubliniensis. The phenolic compound carvacrol showed the highest anti-Candida bioactivity, followed by thymol and isoeugenol. The obtained minimum inhibitory concentration (MIC) values obtained were used in a quantitative structure-activity relationship (QSAR) analysis where the electronic, steric, thermodynamic and topological descriptors served as dependent variables. According to the descriptors obtained in this QSAR study, the antifungal activity of phenols has a first action specific character which is based on their interaction with plasma or mitochondrial membranes. The second action is based on a steric descriptor-the maximal and minimal projection of the area-which could explain the inability of some phenolic compounds to be biotransformed to quinones methylene by Candida species. CONCLUSIONS: According to the descriptors obtained in this QSAR study, the anti-Candida activity of ortho-substituted phenols is due to more than one action mechanism. The anti-Candida activity of phenolic compounds can be predicted by their molecular properties and structural characteristics. SIGNIFICANCE AND IMPACT OF THE STUDY: These results could be employed to predict the anti-Candida activity of new phenolic compounds in the search for new alternatives or complementary therapies to combat against candidiasis.


Assuntos
Antifúngicos/farmacologia , Candida/efeitos dos fármacos , Fluconazol/farmacologia , Fenóis/farmacologia , Antifúngicos/química , Candida/isolamento & purificação , Cimenos , Farmacorresistência Fúngica , Eugenol/análogos & derivados , Eugenol/farmacologia , Humanos , Monoterpenos/farmacologia , Fenóis/química , Relação Quantitativa Estrutura-Atividade , Timol/farmacologia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA