Cromoblastomicose é uma micose crônica que acomete a pele e o tecido subcutâneo. Vários tratamentos têm sido utilizados, mas a eficácia é extremamente baixa, não permitindo eleger uma terapia de escolha. No presente trabalho foram realizados: I – ensaios de suscetibilidade in vitro de agentes da cromoblastomicose contra antifúngicos comerciais; II - caracterização molecular de amostras oriundas de casos clínicos, bem como a descrição destes casos; III - a produção e caracterização de duas nanoemulsões, uma de anfotericina B e uma de itraconazol produzidas pela técnica de homogeneização à alta pressão; IV - a avaliação da atividade antifúngica destas nanoemulsões in vitro e in vivo em agentes da cromoblastomicose; V - a verificação do nível de comprometimento renal e hepático causados pelas nanoemulsões; VI - a avaliação da toxicidade das formulações produzidas. De modo geral, os agentes da cromoblastomicose, apresentaram maior suscetibilidade à terbinafina e ao itraconazol, respectivamente. A combinação de anfotericina B e terbinafina foi sinérgica para quatro dos cinco grupos avaliados. Quanto aos casos clínicos, no primeiro foi identificada uma infecção por E. spinifera e no segundo uma por Fonsecaea monophora. As nanoemulsões foram elaboradas com composição passível de administração parenteral, uma de anfotericina B e uma de itraconazol, pelo método de homogeneização à alta pressão. Não foi possível determinar as CIMs da nanoemulsão de anfotericina B e Abelcet® in vitro, enquanto que a nanoemulsão de itraconazol apresentou CIMs muito semelhantes às do fármaco livre. Em modelo animal de cromoblastomicose, a nanoemulsão de anfotericina B foi mais ativa que o fármaco livre, Fungizone® e Abelcet®. A nanoemulsão de itraconazol também apresentou melhor atividade quando comparada com o fármaco livre. Os níveis de uréia foram mais elevados nos animais que receberam anfotericina B livre e Fungizone®. A enzima alanina aminotransferase foi encontrada em níveis menores nos animais tratados com a nanoemulsão de itraconazol do que naqueles que receberam itraconazol livre. A anfotericina B livre e Fungizone® causaram graves danos aos rins. Nos animais tratados com Abelcet® e com a nanoemulsão de anfotericina B foi possível verificar apenas necrose focal. Da mesma forma, a nanoemulsão de itraconazol protegeu os animais contra danos hepáticos quando comparada com o fármaco livre. Em relação aos ensaios de toxicidade, a anfotericina B foi citotóxica em concentrações a partir de 4μg/mL, sendo que com a nanoemulsão esta toxicidade não foi observada em concentrações mais elevadas. O itraconazol foi citotóxico, sendo que este efeito não foi visto com a nanoemulsão. É de extrema importância a avaliação da suscetibilidade dos agentes da cromoblastomicose a fim de orientar a clínica. A identificação molecular de agentes isolados de casos clínicos pode contribuir para delinear o perfil epidemiológico da doença. As nanoemulsões de anfotericina B e itraconazol apresentaram atividades superiores in vivo quando comparadas aos demais tratamentos e foram capazes de reduzir os efeitos adversos causados por estes antifúngicos. Através de ensaios in vitro foi confirmada a redução da citotoxidade do fármaco quando veiculado na nanoemulsão. Assim, as nanoemulsões produzidas poderiam ser alternativas terapêuticas para o tratamento da cromoblatomicose. / Chromoblastomycosis is a chronic mycosis that affects the skin and subcutaneous tissue. Various treatments have been used, but the efficacy is extremely low and does not allow choosing a therapy of choice. In the present work was performed: I - in vitro susceptibility testing for chromoblastomycosis agents against commercial antifungal; II - molecular characterization of samples from clinical cases as well as the description of these cases III - production and characterization of two nanoemulsions , one of amphotericin B and one of itraconazole, produced by high pressure homogenization technique; IV - assessing the in vitro and in vivo antifungal activity of these nanoemulsions against chromoblastomycosis agents; V - checking the level of impairment caused in the kidney and liver by nanoemulsions; VI - evaluation of toxicity of the formulations produced. In general, the chromoblastomycosis agents showed greater susceptibility to terbinafine and to itraconazole, respectively. The combination of amphotericin B and terbinafine was synergistic to four of the five groups. As for clinical cases, in the first was identified an infection by E. spinifera and in the second one by Fonsecaea monophora. The nanoemulsions were prepared with composition amenable of parenteral administration, one of amphotericin B and one of itraconazole, by the at high pressure homogenization method. Could not be determined the MIC of amphotericin B nanoemulsion and Abelcet® in vitro, while the itraconazole nanoemulsion showed MICs very similar to free drug. In a chromoblastomycosis animal model, the amphotericin B nanoemulsion was more active than free drug, Abelcet® and Fungizone®. The nanoemulsion of itraconazole also showed better activity compared to the free drug. Urea levels were higher in the animals receiving amphotericin B free and Fungizone®. The enzyme alanine aminotransferase was found in lower levels in animals treated with itraconazole nanoemulsion than in those who received itraconazole free. Amphotericin B free and Fungizone® caused severe damage to the kidneys. Already in animals treated with Abelcet® and the amphotericin B nanoemulsion was verified only focal necrosis. Likewise, the itraconazole nanoemulsion protected against liver damage when compared with the free drug. Regarding toxicity assays, amphotericin B was cytotoxic at concentrations from 4 μg/mL, while with the nanoemulsion this toxicity was not observed at higher concentrations. Itraconazole was cytotoxic, and this effect was not observed with the nanoemulsion. It is extremely important to evaluate the susceptibility of chromoblastomycosis agents to guide the clinic. Molecular identification of agents isolated from clinical cases can contribute to outline an epidemiological profile of the disease. The amphotericin B and itraconazole nanoemulsions showed higher activities in vivo when compared to other treatments and were able to reduce the adverse effects caused by these antifungals. Through in vitro assays were confirmed the reduction of the cytotoxicity of the drug when vehiculated in the nanoemulsion. Therefore, the nanoemulsions may be produced therapeutic alternatives for the chromoblastomycosis treatment.

O complexo Sporothrix schenckii reúne espécies etiologicamente relacionadas à esporotricose, uma micose que pode acometer seres humanos e animais. Foi realizada a identificação fenotípica e molecular de 85 isolados provenientes de quatro estados brasileiros (Minas Gerais, Rio de Janeiro, Rio Grande do Sul e São Paulo). Foram pesquisadas a produção de enzimas, o perfil de inibição por leveduras killer, a suscetibilidade aos antifúngicos comerciais e aos extratos de plantas. Os isolados foram identificados como S. schenckii, S. brasiliensis e S. globosa, com predomínio de S. schenckii. Houve discordância de 37,7% entre a identificação das espécies do complexo S. schenckii utilizando metodologias fenotípicas e genotípicas. Entre os antifúngicos testados, a terbinafina foi o fármaco mais ativo; seguido por cetoconazol e itraconazol, enquanto fluconazol e voriconazol foram os menos ativos. Cinco isolados fúngicos foram detectados como resistentes ao itraconazol, sendo um S. globosa e quatro S. schenckii. Não houve diferença nos perfis de suscetibilidade aos antifúngicos entre as espécies do complexo Sporothrix schenckii. Entre os extratos de origem vegetal, o mais ativo foi o proveniente de Pterocaulon polystachyum, mostrando que o uso popular das plantas reforça a importância de pesquisas etnofarmacológicas, abrindo a possibilidade de encontrar novos agentes antifúngicos clinicamente eficazes. Doze das 18 leveduras killer avaliadas apresentaram atividade frente a todos os isolados do complexo S. schenckii estudados. No entanto, não houve diferença na suscetibilidade as toxinas entre as espécies de Sporothrix. Todos os isolados produziram desoxiribonuclease, urease e proteinase. Atividade fosfolipase e esterase foi detectada em 83 (97,6%) e 80 (94,1%), respectivamente, dos isolados testados. Todas as amostras do complexo S. schenckii produziram, pelo menos, quatro das enzimas avaliadas, e 78 (91,8%) dos isolados produziram todas as enzimas analisadas no estudo. No entanto, não foi possível diferenciar as espécies de Sporothrix baseado no perfil enzimático. Entre as enzimas extracelulares avaliadas nos isolados do complexo S. schenckii, desoxiribonuclease e esterase foram produzidas em maior quantidade, podendo vir a ser um fator de virulência. Além disso, o caldo Sabouraud dextrose mostrou potencial para ser usado na avaliação in vitro da atividade antifúngica frente ao complexo S. schenckii. / The Sporothrix schenckii complex combines species etiologically related to sporotrichosis, a mycosis which can affect humans and animals. The phenotypic and genotypic identification of 85 strains from four Brazilian States (Minas Gerais, Rio de Janeiro, Rio Grande do Sul and São Paulo) was performed. The enzymatic production, profile of inhibition by killer yeasts, susceptibility to marketed antifungal and to plant extracts were surveyed. The isolates were identified as S. schenckii, S. brasiliensis and S. globosa, with the predominance of S. schenckii. There was 37.7% disagreement regarding the species classification using phenotypic and genotypic methodologies. Among the tested antifungals, terbinafine was the most active drug, followed by ketoconazole and itraconazole, while fluconazole and voriconazole were the least active ones. Five isolates - one S. globosa and four S. schenckii - were resistent to itraconazole. There was no difference as to the profiles of the susceptibility to the antifungal agents among the Sporothrix species. The most active vegetal extract was from Pterocaulon polystachyum, showing that the popular use of these plants reinforces the importance of ethnopharmacological researches, with the possibility of finding new clinically effective antifungal agents. Twelve out of the 18 evaluated killer yeasts showed activity against all the tested strains of the S. schenckii complex. However, there was no difference in susceptibility to the toxins among the Sporothrix species complex. All the isolates were desoxiribonuclease, urease and proteinase positive. Phospholipase and esterase activities were detected in 83 (97.6%) and 80 (94.1%), respectively, among the isolates evaluated. All the S. schenckii complex strains produced at least four of the evaluated enzymes, and 78 (91.8%) of the isolates produced all the enzymes analyzed in the study. However, it is not possible to differentiate the Sporothrix species based on their enzymatic profile. Among the extracellular enzymes evaluated in the S. schenckii complex isolates, desoxiribonuclease and esterase were the most prominent ones, and their production may be a virulence factor. Furthermore, the Sabouraud dextrose broth showed potential to be used in the in vitro evaluation of the antifungal activity against the S. schenckii complex.

Made available in DSpace on 2014-07-29T16:11:46Z (GMT). No. of bitstreams: 1 fabyla amaral.pdf: 675400 bytes, checksum: 87a47fefd02c9465869b159733685f58 (MD5) Previous issue date: 2010-11-05 / The Brazilian Savanna is recognized as the richest in the world, sheltering more than 6.500 plant species already cataloged, and medicinal uses are attributed to over 220. Species of Myrtaceae family are used in folk medicine in gastrointestinal disorders, infectious diseases and hemorrhagic states, many are known by the presence of essential oils. The objective of this work was the pharmacognostic study of leaves and bark of species Myrcia tomentosa (Aubl.) DC. in order to establish quality parameters and to determine the chemical composition of essential oil (leaves, bark and flowers), as well as to assess the occurrence of seasonal variation between the chemical constituents of essential oil from leaves and to evaluate the antimicrobial activity of leaf essential oil, ethanolic crude extract and fractions from leaf and bark extracts. For this purpose, part of the botanical materials was used in microscopic analysis and in phytochemical analysis. The contents of total phenols, tannins and of total flavonoids were evaluated. The gas chromatography coupled to mass spectrometry (GC / MS) was used to characterize the chemistry of essential oils and the broth microdilution test was used for both evaluation of antimicrobial activity and determination of Minimum Inhibitory Concentration (MIC). In morpho-anatomical study of leaves, it was found that they are simple, leathery and predominantly opposing crossed. Microscopically are hypostomatic with numerous unicellular trichomes, have secretory cavities and idioblasts with prismatic crystals. The bark has flat, curved and sometimes channeled shape. At microscopic level, the bark shows prismatic crystals, sclereids and periderm is formed in the inner layers. In the phytochemical screening, it was found essential oils, tannins and terpenes in leaves and bark, only flavonoids in leaves and saponin in bark. In the essential oils analysis, it was found that (2E, 6E)-Methyl farnesoate is the major component in the flowers and bark essential oils, while the leaves essential oil showed seasonal variation in their chemical composition, with Bicyclogermacrene and (2E, 6E)-Methyl farnesoate as major components The antimicrobial evaluation of leaf essential oil showed activity for Micrococcus roseus, Bacillus subtilis, Bacillus cereus, Micrococcus luteus and Staphylococcus aureus (MIC = 125 - 250 μg/mL) and the fungi Cryptococcus neoformans and Cryptococcus gattii (MIC = 62,5 500 μg/mL); the fractions were moderate activity for most Gram-positive bacteria, and the hexane and dichlorometane fractions of the leaves, and ethyl acetate and aqueous bark were most active (MIC = 250 500 μg/mL). With respect to antifungal activity, the fractions tested showed good or moderate activity for Candida sp (MIC = 15,62 125 μg/mL) and hexanic and dichloromethanic fractions of leaves showed good activity for Cryptococcus sp (MIC = 15,62 62,50 μg/mL). The results contribute to the identification of the species M. tomentosa and demontrate its potential for the treatment of fungal diseases. / O Cerrado brasileiro é reconhecido como a savana mais rica do mundo, abrigando mais de 6.500 espécies de plantas já catalogadas, das quais mais de 220 possuem usos medicinais. Espécies da família Myrtaceae são usadas na medicina popular em distúrbios gastrointestinais, estados hemorrágicos e doenças infecciosas, muitas são conhecidas pela presença de óleos essenciais. O objetivo deste trabalho foi realizar o estudo farmacognóstico das folhas e casca da espécie Myrcia tomentosa (Aubl.) DC. com o intuito de estabelecer parâmetros de qualidade; determinar a composição química do óleo essencial (folhas, casca e flores), bem como avaliar a ocorrência de variação sazonal entre os constituintes químicos do óleo essencial das folhas; e avaliar a atividade antimicrobiana do óleo essencial das folhas, do extrato etanólico bruto e frações das folhas e casca. Para tanto, parte dos materiais botânicos foi utilizada nas análises macro e microscópicas e outra parte nas análises fitoquímicas e nos doseamentos de fenóis totais, taninos e de flavonóides. A Cromatografia Gasosa acoplada à Espectrometria de Massas (CG/EM) foi utilizada para a caracterização química dos óleos essenciais e o teste da microdiluição em caldo para a avaliação da atividade antimicrobiana e determinação da Concentração Inibitória Mínima (CIM). No estudo morfo-anatômico das folhas verificou-se que são simples, coriáceas e predominantemente opostas cruzadas. Microscopicamente são hipoestomáticas, apresentam numerosos tricomas tectores unicelulares, têm cavidades secretoras e idioblastos com cristais prismáticos. A casca possui forma plana, às vezes canaletada e encurvada. Em nível microscópico apresenta cristais prismáticos, esclereides e a periderme é formada nas camadas mais internas. Na triagem fitoquímica foram detectados óleo essencial, taninos e terpenos, tanto nas folhas como na casca, flavonóides apenas nas folhas e saponina apenas na casca. Na análise dos óleos essenciais o (2E,6E)-Metil farnesoato foi o componente majoritário nas flores e casca, enquanto as folhas demonstraram variação sazonal na sua composição química, com Biciclogermacreno e (2E,6E)-Metil farnesoato fazendo parte dos componentes majoritários. Na avaliação antimicrobiana o óleo essencial das folhas demonstrou atividade para Micrococcus roseus, Bacillus subtilis, Bacillus cereus, Micrococcus luteus e Staphylococcus aureus (CIM = 125 250 μg/mL) e para os fungos Cryptococcus neoformans e Cryptococcus gatti (CIM = 62,5 500 μg/mL); as frações tiveram atividade moderada para a maioria das bactérias Gram-positivas, sendo que as frações hexano e diclorometano das folhas, e acetato de etila e aquosa da casca foram as mais ativas (CIM = 250 500 μg/mL); com relação à atividade antifúngica, as frações testadas apresentaram atividade boa ou moderada para Candida sp (CIM = 15,62 125 μg/mL) e as frações hexano e diclorometano das folhas mostraram boa atividade para Cryptococcus sp (CIM = 15,62 62,50 μg/mL). Os resultados obtidos contribuem para a identificação da espécie M. tomentosa e demonstram o seu potencial para o tratamento de doenças fúngicas.

O presente trabalho visou a avaliação do potencial antifúngico de extratos brutos das diferentes partes do vegetal (folha, caule e raiz) de espécies de Piperaceae, os quais foram submetidos ao ensaio de bioautografia frente aos fungos Cladosporium cladosporioides e Cladosporium sphaerospermum. Após a triagem biológica, os extratos brutos das espécies Piper mollicomum, Piper marginatum, Peperomia alata e Peperomia glabella foram selecionados para etapas posteriores de fracionamento e purificação, utilizando-se técnicas cromatográficas. O estudo fitoquímico biomonitorado das espécies selecionadas identificou como metabólitos ativos dois cromenos e uma di-hidrochalcona; duas flavanonas e três fenilpropanóides, sendo um de estrutura inédita, denominado marginatumol; dois policetídeos inéditos, alatanona A e alatanona B; quatro acilresorcinóis e quatro secolignanas, incluindo a peperomina G inédita. Todos os metabólitos isolados apresentaram potencial atividade antifúngica, sendo os policetídeos alatanona A e alatanona B os mais ativos, com atividade superior às substâncias controle (nistatina e miconazol). Assim, os dados obtidos neste estudo permitiram descrever diferentes classes de produtos naturais a partir de uma coleção de extratos de espécies de Piperaceae, com potencial para estudos de relações estrutura-atividade. / The present study was addressed to evaluate the antifungal activity of crude extracts from Piperaceae species in which different parts of the plant (leaves, stems and roots) were assessed by means of bioautography against Cladosporium cladosporioides and Cladosporium sphaerospermum. After antifungal assay, the extratcs from Piper mollicomum, Piper marginatum, Peperomia alata and Peperomia glabella displayed higher growth inhibitory potency and thus were selected for further fractionation and purification using chromatographic techniques. Such dereplication using the bioautographic assay yielded two chromenes and one dihydrochalcone; two flavanones and three phenylpropanoids, including the novel compound marginatumol; two new polyketides, alatanone A and alatanone B; four acylresorcinols and four secolignans, including the novel peperomin G, respectively. The bioautography indicated potential antifungal activity for all isolated metabolites and compounds alatanone A and alatanone B were found the most active in comparison to positive controls (nystatin and miconazole). The bioprospecting approach was proven to be very effective when the isolation of bioactive compounds from a collection of crude extracts is concerned, although not necessarily unraveling the major biosynthetic pathways in each plant species.

[EN] Chitosan films and coatings have been obtained, by incorporating different essential oils (EO) and using different homogenization conditions of the film forming emulsions, in order to obtain antifungal materials for fruit preservation. The effect of oleic acid (OA) on the stability of the initial emulsions and on the film properties was analysed. Coatings were applied to control fungal decay in strawberries. The blending of chitosan with methylcellulose (MC) was also used in coating applications to tomato plants and fruits to prevent fungal infections. The films' functional properties as a function of their composition were analysed, as well as their antimicrobial activity through in vitro and in vivo tests. OA incorporation in the chitosan films (1:1 wt. ratio) reduced water vapour permeability (WVP) values to about 50 % of those of net chitosan films, with a small positive effect of the microfluidization process. EO (cinnamon, thyme and basil) did not notably reduced the WVP values of the chitosan films but a significant improvement in water barrier capacity was induced when OA was also added at 1:1 or 1:0.5 CH:OA ratios. In contrast, lipids slightly promoted oxygen permeability of the films. Lipid addition decreased the film stretchability and stiffness, with a lesser impact on the resistance to break, slightly depending on the droplet sizes. Essential oils also modulated the mechanical behaviour of the films, depending on their composition. Thyme and basil EO greatly promoted film stiffness and resistance to break, whereas cinnamon oil slightly reduced these mechanical attributes. Optical properties of the chitosan films were also affected by lipid incorporation. OA reduced the film transparency and gloss depending on the concentration, but provoked small changes in the colour parameters and whiteness index. EO affected transparency to a lesser extent, but had greater impact on the colour coordinates and whiteness index of the chitosan films due to the selective light absorption of their compounds. EO blend with oleic acid mitigated the colour changes in the films. Likewise, blending of OA with EO significantly reduced the losses of volatiles during the film formation due to the promotion of the stability of the film forming emulsions. Films containing cinnamon EO were effective in reducing the growth of Aspergillus niger, Botrytis cinerea and Rhizopus stolonifer, although thyme and basil EO encapsulated in the films did not exhibit antifungal action against these three fungi. When chitosan-cinnamon EO coatings were applied to strawberries inoculated with R. stolonifer, they reduced the fungal decay of the fruits during 14 days, at 10 °C, at the same time that total coliform counts were maintained at the initial levels. Chitosan coatings with lemon essential oil were also active at controlling fungal decay in strawberries. These did not significantly affect the physicochemical parameters of strawberries throughout cold storage, while they slowed down the respiration rate of the fruits and enhanced the chitosan antifungal activity against B. cinerea. The coatings, with and without lemon EO, affected the strawberry volatile profile, although it was only sensory appreciated for samples coated with chitosan-lemon oil. Blend films of CH and MC (1:1) containing oregano EO caused phytotoxic problems at "3 Leaves" stage of tomato plants, although the total biomass and crop yield was not affected. In the "Fruit" stage, the treatments had no negative effects. Coatings reduced the respiration rate of tomatoes, diminished weight loss during postharvest storage and were effective to decrease the fungal decay of tomatoes inoculated with R. stolonifer. Migration of thymol and carvacrol from CH-MC films in food simulants could overcome the stablished specific migration limit (60 mg/kg) for food contact packaging materials in aqueous and low pH systems if films contain a 1:1 polymer essential oil weight ratio. / [ES] En la presente tesis doctoral se han desarrollado diferentes materiales antifúngicos para su uso en conservación de frutas. Para ello, se han incorporado diferentes aceites esenciales (AE) en recubrimientos y películas de quitosano (Q). Se ha analizado el efecto de la adición de ácido oleico (AO) y las condiciones de homogeneización sobre la estabilidad de las emulsiones y sobre las propiedades de las películas. Se ha estudiado el efecto de los recubrimientos de Q sobre el deterioro fúngico en fresas y el efecto preventivo frente a infecciones fúngicas de las mezclas de metilcelulosa (MC) con Q en plantas de tomate. Se ha estudiado el efecto de la composición de las películas sobre las propiedades funcionales de las mismas, así como su actividad antimicrobiana in vitro e in vivo. La incorporación de AO en las películas de Q (proporción 1:1) redujo la permeabilidad al agua (PVA) en un 50% comparado con la de Q puro. La microfluidización indujo un efecto positivo sobre dicha reducción. La adición de AE (hoja de canela, tomillo o albahaca) no supuso una disminución notable de los valores de permeabilidad obtenidos para las películas de Q. Cuando se añadió AO a las formulaciones de Q y AE (proporciones 1:1 o 1:2), se promovió una mejora significativa en la PVA de las películas. En cambio, la adición de lípidos aumentó ligeramente la permeabilidad al oxígeno, disminuyó la elasticidad y la rigidez, y produjo un menor impacto sobre la resistencia a la rotura. A su vez, la adición de AE modificó el comportamiento mecánico de las películas. Los AE de tomillo y albahaca aumentaron considerablemente la rigidez y la resistencia a la rotura, mientras que el AE de hoja de canela redujo estos parámetros ligeramente. La adición de lípidos a las películas de Q afectó las propiedades ópticas de las mismas. El AO redujo la transparencia y el brillo, en función de la concentración añadida. La adición de AE tuvo un mayor impacto sobre los parámetros de color y el índice de blancura. Las mezclas de AE y AO mitigaron estos cambios de color. Además, la incorporación de las mezclas AE-OA redujo las pérdidas de volátiles del AE durante la formación de las películas. Las películas formuladas con el AE de hoja de canela fueron efectivas contra el crecimientos de A. niger, B. cinerea y R. stolonifer, aunque los AE de tomillo y albahaca encapsulados en las películas no mostraron ninguna actividad antifúngica. La aplicación de los diferentes recubrimientos de Q AE de C en fresas inoculadas con R. stolonifer dio lugar a una reducción en el deterioro fúngico de los frutos almacenados durante 14 días a 10°C. Los recubrimientos de Q-AE de limón también fueron efectivos en el control del deterioro fúngico en fresas. Estos recubrimientos no afectaron significativamente los parámetros físico-químicos de las fresas durante el almacenamiento en refrigeración, disminuyeron la tasa de respiración de los frutos y acentuaron la actividad antifúngica del Q frente a B. cinerea. Tanto los recubrimientos con AE como los de Q puro modificaron el perfil de volátiles de las fresas, aunque estos cambios solo fueron apreciados sensorialmente en el caso de los frutos recubiertos con AE. Las mezclas de Q y MC que contenían AE de orégano causaron efectos fitotóxicos en plantas de tomate en el estadio "3 hojas", aunque no afectaron a la biomasa total. En el estadio "frutos" los tratamientos no tuvieron ningún efecto negativo. Los recubrimientos redujeron la tasa de respiración de los tomates, disminuyeron la pérdida de peso durante el almacenamiento post-cosecha y fueron efectivos contra el deterioro fúngico de tomates inoculados con R. stolonifer. La migración de los compuestos fenólicos timol y carvacrol, contenidos en las películas de Q-MC, podría superar el límite de migración específica establecido (60 mg/Kg) para materiales de envase en contacto con alimentos en los casos de sistemas acuosos y d / [CAT] En la present tesi doctoral s'han desenvolupat diferents materials antifúngics per al seu ús en conservació de fruites. Per a açò, s'han incorporat diferents olis essencials (OE) en recobriments i pel·lícules de quitosano (Q). S'ha analitzat l'efecte de l'addició d'àcid oleic (AO) i les condicions d'homogeneïtzació sobre l'estabilitat de les emulsions i sobre les propietats de les pel·lícules obtingudes. S'ha estudiat l'efecte dels recobriments de Q sobre la deterioració fúngica en maduixes i l'efecte preventiu enfront d'infeccions fúngiques de les mescles de metilcelulosa (MC) amb Q en plantes de tomaca. S'ha estudiat l'efecte de la composició de les pel·lícules sobre les propietats funcionals de les mateixes, així com la seua activitat antimicrobiana in vitro i in vivo. La incorporació de AO en les pel·lícules de Q (1:1) va reduir la permeabilitat al vapor d'aigua (PVA) en un 50% comparat amb la de Q pur. La microfluidització va induir un petit efecte positiu sobre aquesta reducció. L'addició de AE (fulla de canyella, C, timó, T, i alfàbrega, A) no va suposar una disminució notable dels valors de permeabilitat obtinguts per a les pel·lícules de Q. Quan es va afegir AO a les formulacions de Q i AE, es va promoure una millora significativa en la PVA de les pel·lícules. Per contra, l'addició de lípids va augmentar lleugerament la permeabilitat a l'oxigen, va disminuir l'elasticitat i la rigidesa, i va produir un menor impacte sobre la resistència al trencament. Al seu torn, l'addició de OE va modificar el comportament mecànic de les pel·lícules. Els OE de T i d'A van augmentar considerablement la rigidesa i la resistència al trencament, mentre que l'OE de C va reduir aquests paràmetres lleugerament. L'addició de lípids a les pel·lícules de Q també va afectar les propietats òptiques de les mateixes. L'AO va reduir la transparència i la lluentor, en funció de la concentració afegida. L'addició d'OE va tenir un major impacte sobre el paràmetres de color i l'índex de blancor. Les mescles d'OE i AO van mitigar aquests canvis de color. A més, la incorporació de les mescles OE-AO va reduir les pèrdues de volàtils de l'OE durant la formació de les pel·lícules. Les pel·lícules formulades amb l'OE de C van ser efectives contra el creixements d'A. niger, B. cinerea i R. stolonifer, encara que els OE de T i A encapsulats en les pel·lícules no van mostrar cap activitat antifúngica. L'aplicació dels diferents recobriments de Q OE de fulla de canyella en maduixes inoculades amb R. stolonifer va donar lloc a una reducció en la deterioració fúngica dels fruits emmagatzemats durant 14 dies a 10°C. Els recobriments de Q-OE de llimó també van ser efectius en el control de la deterioració fúngica en maduixes. Aquests recobriments no van afectar significativament els paràmetres fisicoquímics de les maduixes durant l'emmagatzematge en refrigeració, van disminuir la taxa de respiració dels fruits i van accentuar l'activitat antifúngica del Q enfront de B. cinerea. Tant els recobriments amb OE com els de Q pur van modificar el perfil de volàtils de les maduixes, encara que aquests canvis sol van ser apreciats sensorialment en el cas dels fruits recoberts amb OE. Les mescles de Q:MC que contenien OE d'orenga van causar efectes fitotòxics en plantes de tomaca en l'estadi "3 fulles", encara que no van afectar a la biomassa total. En l'estadi "fruits" els tractaments no van tenir cap efecte negatiu. Els recobriments van reduir la taxa de respiració de les tomaques, van disminuir la pèrdua de pes durant l'emmagatzematge post collita i van ser efectius contra la deterioració fúngica de tomaques inoculades amb R. stolonifer. La migració dels compostos fenòlics timol i carvacrol, continguts en les pel·lícules de Q-MC, podria superar el límit de migració específica establit (60 mg/Kg) per a materials d'envàs en contacte amb aliments en els casos de sistemes aquosos i d / Perdones Montero, Á. (2015). ANTIFUNGAL CHITOSAN-BASED FILMS AND COATINGS CONTAINING ESSENTIAL OILS FOR FRUIT APPLICATIONS [Tesis doctoral no publicada]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/59413 / TESIS

Les endophytes sont des microorganismes (généralement des bactéries et des champignons) qui vivent dans les tissus végétaux mais n'activent pas le système immunitaire/défense des plantes, contrairement aux pathogènes végétaux qui activent généralement les réponses immunitaires des plantes. Des recherches récentes ont montré que pratiquement toutes les plantes cultivées en plein champ contiennent un certain nombre d'endophytes, et que certains endophytes stimulent la croissance des plantes et renforcent la résistance contre les agents pathogènes. Les endophytes sécrètent des composés chimiques (métabolites secondaires) qui suppriment la croissance des agents pathogènes, un processus connu sous le nom de biocontrôle. En raison de ces propriétés de biocontrôle, les endophytes sont une alternative potentielle aux pesticides chimiques pour lutter contre les maladies des plantes. En conséquence, le biocontrôle est devenu un domaine de recherche important. Mon projet de recherche comportait les objectifs spécifiques suivants : (i) isoler les endophytes des plants de canneberges acquis auprès de deux producteurs commerciaux de canneberges de la variété Stevens situés au Québec, Canada (Bieler Cranberries Inc, et Gillivert Inc.) ; (ii) tester l'activité de biocontrôle des endophytes contre une collection de champignons pathogènes et ensuite inoculer les endophytes les plus actifs dans des plants de canneberges obtenus par germination de la variété Stevens (Bieler Cranberries Inc. ) et Scarlet Knight (Daniele Landreville) ; et (iii) identifier des groupes de gènes de métabolites secondaires en séquençant, assemblant et annotant le génome d'un endophyte qui présentait de fortes caractéristiques de biocontrôle. Dans le cadre de ce projet de recherche, des tests antagonistes in vitro ont été réalisés avec des endophytes de la canneberge et un champignon pathogène, qui ont montré que Pseudomonas sp. CSWB3, Pseudomonas sp. CLWB12 et la souche fongique Lachnum sp. EFK28 étaient les plus actifs et ces souches ont donc été sélectionnées pour des études plus approfondies. Des expériences de germination de semis in vitro et d'inoculation d'endophytes ont montré que les souches bactériennes Pseudomonas sp. CSWB3 et Pseudomonas sp. CLWB12 amélioraient la croissance des semis de canneberges de la variété Stevens. Comme les Pseudomonas sp. CSWB3 et Pseudomonas sp. CLWB12 ont tous deux un effet antagoniste élevé sur les champignons pathogènes, un seul (Pseudomonas sp. CSWB3) a été soumis à une analyse du génome. Le séquençage, l'assemblage, l'annotation et l'analyse du génome de Pseudomonas sp. CSWB3 a révélé que cette souche possède cinq groupes de gènes biosynthétiques de métabolites secondaires qui codent pour les protéines responsables de la biosynthèse des composés antifongiques/antimicrobiens : pyrrolnitrine, pyoluteorine, putisolvine, 2,4-diacétylephloroglucinol, bicornutine A1 et bicornutine A2. Sur la base des résultats de ces travaux, nous concluons que certains endophytes de la canneberge qui possèdent des groupes de gènes codant pour des métabolites secondaires antifongiques peuvent supprimer les pathogènes fongiques et améliorer la croissance des plantes. / Endophytes are microorganisms (typically bacteria and fungi) that live within plant tissue but do not activate the plant defense/immune system, unlike plant pathogens that typically do activate plant immune responses. Recent research has shown that virtually all plants grown under field conditions contain a number of endophytes, and that certain endophytes stimulate plant growth and enhance resistance against pathogens. Endophytes secrete chemical compounds (secondary metabolites) that suppress pathogen growth, a process known as biocontrol. Because of these biocontrol properties, endophytes are a potential alternative to chemical pesticides for combatting plant disease. Accordingly, biocontrol has become an important field of research. My research project was comprised of the following specific aims: (i) isolate endophytes from cranberry plants that were acquired from two commercial producers of cranberries of the Stevens variety located in Quebec, Canada (Bieler Cranberries Inc, and Gillivert Inc.); (ii) test the biocontrol activity of endophytes against a collection of fungal pathogens and then inoculate the most active endophytes into cranberry seedlings that were obtained by germinating Stevens (Bieler Cranberries Inc.) and Scarlet Knight (Daniele Landreville) seeds; and (iii) identify secondary metabolite gene clusters by sequencing, assembling, and annotating the genome of one endophyte that exhibited strong biocontrol characteristics. As part of this research project, in vitro antagonistic tests were conducted with cranberry endophytes and fungal pathogen, which showed that Pseudomonas sp. CSWB3, Pseudomonas sp. CLWB12, and the fungal strain Lachnum sp. EFK28 were the most active and therefore these strains were selected for further studies. In vitro seedling germination and endophyte inoculation experiments showed that the bacterial strains Pseudomonas sp. CSWB3 and Pseudomonas sp. CLWB12 enhanced the growth of cranberry seedlings of the Stevens variety. Since Pseudomonas sp. CSWB3 and Pseudomonas sp. CLWB12 both had a high antagonistic effect on fungal pathogens, only one (Pseudomonas sp. CSWB3) was subjected to genome analysis. Sequencing, assembly, annotation, and analysis of the Pseudomonas sp. CSWB3 genome revealed that this strain possesses five secondary metabolite biosynthetic gene clusters that encode proteins responsible for the biosynthesis of the antifungal/antimicrobial compounds pyrrolnitrin, pyoluteorin, putisolvin, 2,4-diacetylephloroglucinol, bicornutin A1, and bicornutin A2. Based on the results of this work, we conclude that certain cranberry endophytes that possess gene clusters encoding antifungal secondary metabolites can suppress fungal pathogens and enhance plant growth.