113 resultados para tomato leafminer.
Resumo:
Phytomonas serpens are flagellates in the family Trypanosomatidae that parasitise the tomato plant (Solanum lycopersicum L.), which results in fruits with low commercial value. The tomato glycoalkaloid tomatine and its aglycone tomatidine inhibit the growth of P. serpens in axenic cultures. Tomatine, like many other saponins, induces permeabilisation of the cell membrane and a loss of cell content, including the cytosolic enzyme pyruvate kinase. In contrast, tomatidine does not cause permeabilisation of membranes, but instead provokes morphological changes, including vacuolisation. Phytomonas treated with tomatidine show an increased accumulation of labelled neutral lipids (BODYPY-palmitic), a notable decrease in the amount of C24-alkylated sterols and an increase in zymosterol content. These results are consistent with the inhibition of 24-sterol methyltransferase (SMT), which is an important enzyme that is responsible for the methylation of sterols at the 24 position. We propose that the main target of tomatidine is the sterols biosynthetic pathway, specifically, inhibition of the 24-SMT. Altogether, the results obtained in the present paper suggest a more general effect of alkaloids in trypanosomatids, which opens potential therapeutic possibilities for the treatment of the diseases caused by these pathogens.
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Heterobathmia pseuderiocrania Kristensen & Nielsen (Lepidoptera, Heterobathmiidae): identification based on DNA-barcoding and notes on the morphology and life history of the immature stages. The larva morphology of the species Heterobathmia pseuderiocrania (Lepidoptera, Heterobathmiidae), a Nothofagus obliqua leafminer in Chile, is described. The tissue-feeding first and last instars are described. Also, the number of larval stages, some aspects of the biology and life cycle of the species are provided.
Resumo:
Calycomyza hyptidis Spencer (Diptera, Agromyzidae): descriptions, redescriptions and first record in Ocimum basilicum (Lamiaceae) in Brazil. All phases of the leafminer Calycomyza hyptidis Spencer are for the first time described, including the larva, puparium and adult female. Illustrations are presented for male and female terminalia, mine, larva and pupa. The species is first recorded in leaves of Ocimum basilicum L. (Lamiaceae) in Brazil.
Resumo:
O objetivo deste trabalho foi integrar dados de caracteres quantitativos, multicategóricos, moleculares e fitopatológicos para a avaliação da diversidade genética de subamostras de tomateiro do Banco de Germoplasma de Hortaliças da Universidade Federal de Viçosa (BGH-UFV). Foram utilizados dados de 67 subamostras de tomateiro do BGH-UFV, caracterizadas quanto a 19 caracteres quantitativos, 30 multicategóricos, 52 locos ISSR e à reação a três patógenos (Alternaria solani, Pseudomonas syringae pv. tomato e Tomato yellow spot virus). Inicialmente, a avaliação da diversidade entre as subamostras foi realizada para cada conjunto de caracteres individualmente, e indicou que a diversidade baseada em qualquer um dos conjuntos de dados não reflete a diversidade dos demais. Para a integração dos dados, codificaram-se os de natureza quantitativa em multicategóricos, por meio de cinco estratégias diferentes. A estratégia de divisão equitativa da amplitude dos dados em três classes foi a mais indicada, com correlação de 0,78 entre as matrizes de dissimilaridade dos dados codificados e originais. A análise de diversidade genética a partir da integração dos dados resultou em grupos com maior correspondência às origens das subamostras de tomateiro avaliadas, o que indica que a integração de dados de diferentes naturezas pode ser realizada com êxito pela conversão dos dados quantitativos em multicategóricos.
Resumo:
In this study, different solutions to extract vitamin C were tested. High-performance liquid chromatography was chosen and the conditions were based on isocratic elution in reverse phase column. Dehydroascorbic acid was determined indirectly after its reduction using dithiothreitol. The use of metaphosphoric acid to stabilize the vitamin C was shown to be required and it was necessary to neutralize the pH of the extract to apply dithiothreitol. The average recovery was 90% in collard and tomato samples. The presence of oil did not interfere in extraction and the methodology can be used to analyze stir fried vegetables.
Resumo:
This work was aimed on optimization of the matrix solid-phase dispersion (MSPD) technique using gas chromatography for analyzing residues of chlorpyriphos, λ-cyhalothrin, cypermethrin and deltamethrin in tomatoes. The results showed that silica was more efficient for the clean up of extracts, but florisil provided the highest recovery rates. A 2³ complete factorial design was carried out to evaluate the absorbent/sample ratio, presence of co-column (silica) and ultrasonic bath on the extraction rate. The percentage of extraction of the pesticides chlorpyriphos, λ-cyhalothrin, cypermethrin and deltamethrin were 64.7, 88.3, 99.2 and 89.2%, respectively, with relative standard deviations below 5%.
Resumo:
Multiresidue methods for pesticides monitoring by GC are commonly employed, however, it is well known that the presence of compounds of the matrix introduces errors during the quantiûcation. The main consequence of matrix effect is an increasing or decreasing analyte signal after the GC saturation with extracts of matrix. In this paper, the influence of constituents of nine matrices on the quantification of the four pesticides by GC-ECD was studied. Variation of signal was evaluated by PCA and HCA, and results showed that the constituents of tomato increased the signal (until 300%), while extracts of apple decreased (until -20%). Variation the analyte signal in the presence of the matrix in respect to the same analyte in solvent (standard solution) also was observed, mainly for liver extract (until 270%).
Resumo:
A method to quantify lycopene and β-carotene in freeze dried tomato pulp by high performance liquid chromatography (HLPC) was validated according to the criteria of selectivity, sensitivity, precision and accuracy, and uncertainty estimation of measurement was determined with data obtained in the validation. The validated method presented is selective in terms of analysis, and it had a good precision and accuracy. Detection limit for lycopene and β-carotene was 4.2 and 0.23 mg 100 g-1, respectively. The estimation of expanded uncertainty (K = 2) for lycopene was 104 ± 21 mg 100 g-1 and for β-carotene was 6.4 ± 1.5 mg 100 g-1.
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This paper presents a practical and rapid method which was validated for simultaneous quantification and confirmation of 29 pesticides in fruits and vegetables using ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). The samples were extracted following the method known as QuEChERS. Using the developed chromatographic conditions, the pesticides can be separated in less than 9 min. Two multiple reaction monitoring (MRM) assays were used for each pesticide. Four representative matrices (lettuce, tomato, apple and grapes) were selected to investigate the effect in recoveries and precision. Typical recoveries ranged from 70-120%, with relative standard deviation (RSDs) lower than 20%.
Resumo:
Transcriptase reverse - polymerase chain reaction (RT-PCR) and dot blot hybridization with digoxigenin-labeled probes were applied for the universal detection of Tospovirus species. The virus species tested were Tomato spotted wilt virus, Tomato chlorotic spot virus, Groundnut ringspot virus, Chrysanthemum stem necrosis virus, Impatiens necrotic spot virus, Zucchini lethal chlorosis virus, Iris yellow spot virus. Primers for PCR amplification were designed to match conserved regions of the tospovirus genome. RT-PCR using distinct primer combinations was unable to simultaneously amplify all tospovirus species and consistently failed to detect ZLCV and IYSV in total RNA extracts. However, all tospovirus species were detected by RT-PCR when viral RNA was used as template. RNA-specific PCR products were used as probes for dot hybridization. This assay with a M probe (directed to the G1/G2 gene) detected at low stringency conditions all Tospovirus species, except IYSV. At low stringency conditions, the L non-radioactive probe detected the seven Tospovirus species in a single assay. This method for broad spectrum detection can be potentially employed in quarantine services for indexing in vitro germplasm.
Resumo:
The fungus Stemphylium solani causes leaf blight of tomato (Lycopersicon esculentum) in Brazil. In recent years, severe epidemics of a new leaf blight of cotton (Gossipium hyrsutum) caused by S. solani occurred in three major cotton-growing Brazilian states (PR, MT and GO). Molecular analysis was performed to assess the genetic diversity among the S. solani isolates from cotton, and to verify their relationship with representative S. solani isolates from tomato. Random amplified polymorphic DNA (RAPD) markers and internal transcribed spacers of ribosomal DNA (rDNA) were used to compare 33 monosporic isolates of S. solani (28 from cotton and five from tomato). An isolate of Alternaria macrospora from cotton was also used for comparison. RAPD analysis showed the presence of polymorphism between the genera and the species. The A. macrospora and the S. solani isolates from cotton and tomato were distinct from each other, and fell into separate groups. Variation by geographic region was observed for the tomato isolates but not for the cotton isolates. Amplifications of the ITS region using the primer pair ITS4/ITS5 resulted in a single PCR product of approximately 600 bp for all the isolates. Similarly, when amplified fragments were digested with eight restriction enzymes, identical banding patterns were observed for all the isolates. Hence, rDNA analysis revealed no inter-generic or intra-specific variation. The genetic difference observed between the cotton and the tomato isolates provides evidence that S. solani attacking cotton in Brazil belongs to a distinct genotype.
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The cubiu (Solanum sessiliflorum) fruit, originating in the Amazon basin, is commonly used in that region for food, medicine, and cosmetics. In an experimental culture of cubiu, in order to evaluate its adaptation to conditions in the Northern region of the state of Rio de Janeiro, it was observed plants with mosaic symptoms. A cubiu plant was collected and analyzed to identify the etiological agent. After mechanical passage through a local lesion host, a host range test was performed. The virus induced chlorotic local lesions in Chenopodium quinoa, necrotic local lesions in Gomphrena globosa, mosaic in S. sessiliflorum, leaf and stem necrosis in tomato (Lycopersicon esculentum) 'Rutgers', mosaic and leaf distortion in Datura stramonium and Physalis floridana, and necrotic local lesions followed by systemic necrosis and plant death in four Nicotiana species. Electron microscopic observations of ultra thin sections from infected cubiu leaves showed the presence of spheroidal, membrane-bound particles typical of tospovirus species. Analysis of the nucleocapsid protein from concentrated virus particles indicated the presence of a 28 kDa protein. RT-PCR was performed after total RNA extraction from infected IPA-6 tomato leaves. A fragment of approximately 0,8 kbp corresponding to the N gene was amplified, cloned and sequenced. The N protein from the cubiu isolate was 95% homologous to the Groundnut ringspot virus (GRSV) protein, and no more than 85% homologous to those from Zucchini lethal chlorosis virus (ZLCV) and Chrysanthemun stem necrosis virus (CSNV), Tomato spotted wilt virus (TSWV), and Tomato chlorotic spot virus (TCSV). This is the first report of the occurrence of GRSV (or any other plant virus) in cubiu.
Resumo:
Plantas de tomateiro (Lycopersicon esculentum) apresentando sintomas de amarelecimento do limbo foliar principalmente nas nervuras, redução de crescimento e distorções foliares foram coletadas em lavouras do cinturão verde de Campinas, São Paulo, e mantidas no Centro Experimental de Campinas (IAC), para utilização em experimentos de avaliação de resistência de genótipos à virose. A partir de análises moleculares, o vírus foi identificado como Tomato yellow vein streak virus (TYVSV). Foram feitas avaliações em campo (infecção natural) e em telado (infecção natural e controlada), usando-se diversos genótipos, abrangendo cultivares, híbridos, linhagens e populações, além de espécies selvagens de tomateiro. Alguns dos genótipos e híbridos contêm o gene de resistência Ty-1. Em campo, destacou-se o híbrido 'BX 1016158' com as menores incidências de doença. Em telado (infecção natural), híbridos interespecíficos de L. esculentum x L. peruvianum, e a linhagem PI 134417 (L. hirsutum) mostraram-se os mais resistentes ao isolado. O método de avaliação precoce em telado (infecção controlada) mostrou-se adequado para discriminar genótipos resistentes ao isolado. Por meio desse método, constatou-se a resistência das linhagens 'LA 444-1' (L. peruvianum), F4(TySw5) e a série IAC 14-2, e dos híbridos 'Franco' e BX1653088 ('Densus'), os quais receberam notas próximas de um ou não apresentaram sintomas.
Resumo:
O gênero Erigeron (Asteraceae), de plantas da vegetação espontânea, encontra-se amplamente disseminado nas regiões Sul e Sudeste do Brasil, sendo freqüentemente encontrado em lavouras perenes e anuais. Plantas de E. bonariensis com sintoma de mosaico, típico do induzido por vírus, foram coletadas no município de São Paulo e submetidas a análises ao microscópio eletrônico de transmissão, testes biológicos, sorológicos e moleculares. Em cortes ultrafinos do tecido foliar original, observaram-se inclusões tubulares e cata-ventos dispersos no citoplasma. Através de inoculação mecânica, somente Chenopodium amaranticolor, C. quinoa, Nicotiana benthamiana e N. clevelandii foram infetadas. Os resultados obtidos em ELISA foram negativos quando se utilizaram antissoros contra o Turnip mosaic vírus (TuMV) e diferentes estirpes do Potato virus Y (PVY), constatando-se relacionamento sorológico com o Lettuce mosaic virus (LMV). Com a utilização de oligonucleotídeos específicos para LMV amplificaram-se fragmentos esperados de aproximadamente 280 pb, que seqüênciados confirmaram a identidade do vírus. A ocorrência do LMV em E. bonariensis, gênero da mesma família botânica da alface (Lactuca sativa), é de grande importância, pois talvez possa atuar como reservatório para infecção de campos de produção de alface. Este é o primeiro relato, no Brasil, de vírus infetando Erigeron sp., o qual só havia sido reportado como hospedeira natural do Bidens mottle virus (BiMoV) e do Tomato spotted wilt virus (TSWV) nos Estados Unidos.
Resumo:
No estudo da interação de um begomovírus isolado de tomateiro (Lycopersicon esculentum) em Anápolis-GO, denominado GO-ANPL (taxonomicamente relacionado ao Tomato rugose mosaic virus, ToRMV) com o vetor Bemisia tabaci biótipo B, determinaram-se o período de acesso de aquisição do vírus (PAA), o período de acesso de inoculação (PAI), o período de latência (PL), a sua retenção e transmissão à progênie. Nos experimentos empregaram-se plantas de tomateiro 'Santa Clara' e cinco insetos por planta. Constatou-se um PAA mínimo de 15 min com o qual 6% dos tomateiros foram infetados. Este percentual aumentou para 65% quando o PAA foi estendido para 24 h. O PAI mínimo foi de 30 min registrando-se 18% de infecção, o qual foi elevado para 67% com 24 h de PAI. Observou-se o término do PL 16 h após o vetor adquirir o vírus. Na detecção do GO-ANPL no vetor via PCR, testes com mais de 2.500 espécimens constataram o vírus em ninfas desenvolvidas em tomateiro infetado, em adultos com diferentes PAAs, mas não em ovos de fêmeas avirulíferas ovipositados em planta infetada. Observou-se a passagem transestadial em 100% dos adultos testados que transmitiram o vírus em 33% dos casos. Evidenciou-se a transmissão à progênie pela detecção do vírus em ovos, ninfas e adultos provenientes de fêmeas virulíferas, contudo, a transmissão do vírus pelos adultos não foi observada. Os resultados obtidos indicam que a interação vírus-vetor é estabelecida desde a fase inicial do desenvolvimento do inseto e podem ser considerados relevantes para os estudos epidemiológicos dos begomovírus associados ao biótipo B de B. tabaci no país.