The electrospinning has been widely used in tissue engineering for the preparation of wound dressing with the most varied polymers and drugs. Considering that propolis has antimicrobial and anti-inflammatory characteristics, the aim was to develop electrospun fibers from PBAT (poly (butylene-adipate-co-terephthalate)/PCL (poly(ε-caprolactone) containing propolis in order to promote antimicrobial action and the healing of wounds. By the optical microscopy analysis, the best parameter for obtaining the fibers was chosen: 16.5% (v/v) of propolis extract alcoholic solution, 14.0 cm needle-collector distance, 17.0 kV of voltage and 0.5 mL h-1 flow rate. The scanning electron microscopy demonstrated fiber diameters of 0.51 ± 0.12 μm for the polymer blend and 1.16 ± 0.98 μm for the blend with propolis. The Fourier transform infrared spectroscopy (FTIR) results showed no evidence of chemical interaction with propolis, this being a physical interaction. This interaction was corroborated by the differential scanning calorimetry (DSC) due to the variation in the heats involved, mainly in the aromatic part of the polymer blend, indicating a better interaction in the PBAT group. Finally, it was found that fibers presents propolis antimicrobial activity against the bacteria Pseudomonas Aeruginosa. The results indicate that this blend has a great potential to be used as a cutaneous dressing.

Abstract INTRODUCTION: Knowledge of triatomine bloodmeal sources is essential for understanding vector-host interactions in Trypanosoma cruzi transmission cycles. Expensive commercial deoxyribonucleic acid (DNA) extraction kits are widely used for bloodmeal identification. This study assessed the performance of an inexpensive phenol-chloroform DNA extraction protocol for identification of triatomine bloodmeal sources, comparing it with a commercially available kit. METHODS: Both methods were used to obtain DNA from the intestinal contents of Triatoma brasiliensis blood-fed on either Columba sp., Mus musculus, or Gallus gallus. Subsequently, the mitochondrial 12S ribosomal ribonucleic acid (rRNA) gene was amplified by polymerase chain reaction, sequenced, and compared with GenBank data. RESULTS: Twelve (80%) samples extracted with the commercial kit and four (26.7%) with phenol-chloroform were pure (according to the A260/A280 ratio). Samples extracted with phenol-chloroform, except for Columba sp. samples, had higher DNA concentration than those extracted with the commercial kit. Samples extracted using phenol-chloroform and blood-fed on G. gallus had significantly higher DNA concentration than those blood-fed on Columba sp. (p-value <0.001) and M. musculus (p-value <0.001). The 215-base-pair 12S rRNA fragment was amplified from all samples and produced reliable sequences, enabling the identification of the bloodmeal source, most of which showed identity and coverage above 95%. The phenol-chloroform method was much less expensive than the commercial kit but took considerably more time to perform. CONCLUSIONS: Our data showed that both DNA extraction methods produced reliable sequences enabling identification of triatomine bloodmeal sources but differed greatly in cost and time required.

No presente, foi avaliada a influência do amendoim-forrageiro cv. Amarillis e da gramínea coastcross nas entrelinhas de plantas de laranjeira 'Natal' quanto à produção e liberação de ascósporos de G. citricarpa, e consequente controle da mancha-preta dos frutos cítricos. Os tratamentos avaliados foram: 1- cultivo convencional, sem utilização de fungicidas; 2- cultivo convencional, com utilização de fungicidas; 3- gramínea coastcross, e 4- amendoim forrageiro entre as linhas das plantas. O monitoramento de ascósporos deu-se mediante armadilhas caça-esporos do tipo Quest Volumetric Spore System™. Um total de 33 inspeções foi realizado semanalmente, a partir do final de agosto até início de setembro do ano seguinte. A quantificação da doença deu-se mediante utilização de escala diagramática de notas, sendo também determinada a porcentagem de frutos com padrão comercial. A gramínea coastcross foi o melhor tratamento em reduzir o número de ascósporos liberados, diferindo, estatisticamente, do convencional, porém não dos demais tratamentos. Cultivo intercalar e cultivo convencional associado com aplicações de fungicida foram os mais eficientes quanto à redução da severidade de sintomas da mancha-preta, diferindo do tratamento- -testemunha, sem emprego de fungicida. Esses tratamentos foram os que também proporcionaram a maior porcentagem de frutos com padrão comercial, sendo de 89% a 91%, enquanto no cultivo convencional, sem uso de fungicidas, foi de 73%.

This study highlighted the effect of planting coast-cross grass and forage peanut cv. Amarilis between rows of Natal oranges on spreading of Guignardia citricarpa ascospores and consequent citrus black spot control. Treatments evaluated were: 1- conventional cultivation, free of fungicides; 2- conventional cultivation, using protective fungicides; 3- inter-crop cultivation of coast-cross grass between rows of citrus crops and; 4- inter-cropping cultivation of forage peanut between the rows of citrus crops. Quest Volumetric Spore SystemTM traps were set in order to determine the number of ascospores released. A total of 33 inspections were conducted weekly, from the end of August until early September the following year. A diagrammatic scale was used to determine the severity of the disease as well as the percentage of fruits having a commercial standard. The coast-cross grass was more effective in reducing the number of ascospores produced, whose average statistics were lower than in the conventional treatments, free-fungicides. The inter-crop and conventional cultivation method coupled with fungicide treatment was more effective in reducing the severity of citrus black spot symptoms, and differs statistically from the fungicide-free control method. These methods also resulted in a higher percentage of fruits of a commercial standard, ranging from the 89% through the 91% percentile, and the cultivation, free of fungicides, fell within the 73%.

Fungos do gênero Guignardia são frequentemente isolados em diferentes espécies de plantas, sendo muitas vezes caracterizados como fungos endofíticos. Entretanto, algumas espécies deste fungo, a exemplo de G. citricarpa e G. psidii, são causadores de importantes doenças que afetam culturas agrícolas, como a Mancha-Preta dos Citros (MPC) e a podridão dos frutos de goiabeira, respectivamente. Também são apontados como causadores de manchas foliares em diferentes espécies de frutíferas e também em outras culturas. Este trabalho teve o objetivo de isolar, identificar e caracterizar a diversidade genética existente entre isolados de Guignardia oriundos de citros, mangueira, goiabeira, eucaliptos, jabuticabeira e pitangueira através da análise da sequência de DNA do cístron ITS1-5,8-S-ITS2. Verificou-se que os isolados obtidos pertencem às espécies G. citricarpa e G. mangiferae. Entretanto, dois grupos encontrados em mangueira não puderam ser identificados em nível de espécie com base em sua sequência de DNA em função da baixa similaridade com as sequências de diferentes espécies de Guignardia já depositadas em banco de dados. Desta forma, goiabeira, eucaliptos, jabuticabeira e pitangueira são hospedeiras de G. mangiferae, enquanto os citros hospedam duas formas, G. citricarpa e G. mangiferae. Já a mangueira é hospedeira de G. mangiferae e de dois outros grupos ainda não identificados. Verificou-se ainda que isolados de Guignardia obtidos de sintomas de podridão de fruto de goiabeira foram identificados como G. mangiferae.

Fungi of Guignardia genera are commonly isolated from different plant species and most of the time they are characterized as endophytics. However, some species of this genus, as G. citricarpa and G. psidii are known as causal agents of serious diseases that affect cultures, such as the Citrus Black Spot and the guava fruit rot, respectively. They are also responsible for diseases that cause foliar spots in different fruit species and also in other cultures. This work has the objective of isolate, identify and characterize the genetic diversity present among Guignardia isolates obtained from citrus, mango, guava, eucalyptus, Brazilian grape tree and Surinam cherry by analysis of DNA sequence from cístron ITS1-5,8SITS2. It was verified that the obtained isolates belong to G. mangiferae and G. citricarpa species. Two different Guignardia types, that were found in mango, could not be identified in species, and do not belong to none of the species deposited in GenBank. So, this work found that mango, guava, eucalyptus, Brazilian grape tree and Surinam cherry host only G. mangiferae, whereas citrus hosts G. mangiferae and G. citricarpa species. Mango hosts three different Guignardia, G. mangiferae and two others types that remain without identification of the species level. It was also verified that isolates of Guignardia obtained from guava fruit rot symptoms were identified as G. mangiferae.

Este trabalho objetivou avaliar a infecção natural de morcegos por tripanosomatídeos. Foram examinados, por hemocultura, 86 exemplares de diferentes gêneros, sendo 22 (25,58%) amostras isoladas de Desmodus rotundus e Lonchorhina aurita. Os resultados obtidos contribuem para o conhecimento da ocorrência de tripanosomatídeos em morcegos no Estado do Rio de Janeiro.

This study aimed to evaluate natural infection of bats by trypanosomatids. Using blood culturing, 86 specimens from different genera were examined, and 22 samples (25.58%) of Desmodus rotundus and Lonchorhina aurita were isolated. These results contribute towards knowledge of the occurrence of trypanosomatids in bats in the State of Rio de Janeiro.

A investigação fitoquímica do extrato metanólico das folhas de Annona dioica (Annonaceae) resultou na identificação dos flavonóides kaempferol (1), 3-O-[3",6"-di-O-p-hidroxicinamoil] -beta-galactopiranosil-kaempferol (2), 6"-O-p-hidroxicinamoil-beta-galactopiranosil-kaempferol (3) e 3-O-beta-galactopiranosil-kaempferol (4). As estruturas foram caracterizadas inequivocamente através de análises espectroscópicas utilizando-se RMN de ¹H e 13C uni e bi-dimensional. Os efeitos citotóxicos dos flavonóides e da fração flavonoídica (FF) foram avaliados frente a células do carcinoma de Ehrlich, utilizando-se o ensaio do MTT (brometo de 3-(4,5-dimetiltiazol-2-il)-2,5-difeniltetrazolium). Os resultados indicaram que 1, 2, 3 e FF apresentam ação anti-proliferativa importante quando comparados com a quercetina. A ação inibitória dos flavonóides sobre as DNA-topoisomerases I e II foi avaliada utilizando-se o ensaio de relaxação sobre o plasmídeo pBR322. Os resultados indicaram ação não seletiva dos flavonóides sobre as DNA-topoisomerases I e II.

Chemical investigation of methanol extract leaves from Annona dioica (Annonaceae) resulted in the identification of flavonoids kaempferol (1), 3-O-[3",6"-di-O-p-hydroxycinnamoyl]-beta-galactopyranosyl-kaempferol (2), 6"-O-p-hydroxycinnamoyl-beta-galactopyranosyl-kaempferol (3) and 3-O-beta-galactopyranosyl-kaempferol (4). The structures were unequivocally characterized by ¹H and 13C NMR spectroscopic analyses using 1D and 2D experiments. The cytotoxic effects of the flavonoids and flavonoid fraction (FF) were evaluated by MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay against Ehrlich carcinoma cells. The results indicated that 1, 2, 3 and FF exhibit significant antiproliferative action when compared to quercetin. The inhibitory action on DNA-topoisomerase I and II of all the flavonoids was evaluated by relaxation assays on pBR322 plasmid DNA. The results indicated the inhibitory and non-selective effects of the flavonoids on DNA-topoisomerase I and II.

Diversas espécies do gênero Solanum apresentam glicoalcalóides e flavonóides com grande variedade de atividades biológicas. O flavonóide tiliroside (1), uma fração rica em glicoalcalóides denominada GB e o glicoalcalóide solasonina (2) foram obtidos dos tricomas de galhos jovens e frutos de Solanum crinitum Lam e o alcalóide estereoidal solasodina (3), extraído das partes aéreas de S. jabrense Agra & M. Nee, tiveram sua atividade citotóxica avaliada frente a células do carcinoma de Ehrlich e da leucemia humana K562. O efeito antiproliferativo destas substâncias mostrou comportamento dose-dependente após avaliação através do método do MTT, para ambos os casos. Os resultados indicaram atividade citotóxica para 1, GB e 2, com IC50 = 69,50 mM, 19,5 mg mL-1 e 74,20 mM, respectivamente, quando ensaiadas frente ao carcinoma de Ehrlich, e IC50 = 118,40 mM, 13,65 mg mL-1, 60,35 mM e 76,92 mM para 1, GB, 2 e 2a (derivado peracetilado da solasonina) frente a leucemia K562. A baixa atividade da aglicona solasodina (3) indicou a importância da presença dos açúcares na estrutura do glicoalcalóide e permitiu postular a substância 2, presente na fração rica em glicoalcalóides (GB), como um dos principios ativos. Além disso, os resultados mostraram a possibilidade de biomonitoramento através do ensaio do MTT na busca de metabólitos com atividade citotóxica.

Steroidal alkaloids, flavonoids and their glycosides occurring in numerous species of Solanum genus are known to possess a variety of biological activities. The flavonoid tiriloside (1), a rich in glycoalkaloids total fraction named GB and the glycoalkaloid solasonine (2) isolated from thricomes of young branches and fruits from Solanum crinitum Lam, and the aglycone solasodine (3) isolated from Solanum jabrense Agra & M. Nee, were assayed against murine Ehrlich carcinoma and human K562 leukaemia cultured cells. The exposure in vitro of these cancer cells to these products resulted in a dose-dependent growth inhibition evaluated by the MTT method. The results indicated significant cytotoxic activities with IC50 = 69.50 mM, 19.5 mg mL-1, and 74.20 mM for 1, GB and 2, respectively, against Ehrlich carcinoma, and IC50 = 186.50 mM, 13.65 mg mL-1 and 76.92 mM, for 1, GB, 2 and 2a, respectively, against K562 leukaemia cells. The low activity of the aglycone 3 indicates that the role of the sugar moiety is very important in the cytotoxic activity of glycoalkaloid solsonine. The cytotoxic activity revealed by the GB fraction may be attributed to the presence of 2. Additionally, these results show the viability of the MTT assay for monitoring phytochemical bioactive compounds.