1000 resultados para Tomato chlorotic mottle virus
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Vírus do gênero Begomovirus são transmitidos por mosca-branca Bemisia tabaci G., e constituem um dos problemas fitossanitários sérios em diversas culturas. Plantas de pimentão coletadas em oito regiões do Estado de São Paulo, foram submetidas a extração de DNA total e PCR com primers universais e degenerados para begomovírus, que amplificam parte da região codificadora para a proteína capsicial. Os dados indicam a presença de begomovírus em pimentão nas cinco regiões coletadas. Análise das seqüências do DNA viral e análise filogenética revelaram identidade com dois begomovírus nativo da América. Tomato severe rugose virus - ToSRV (AY029750) e com Tomato yellow vein streak virus (ToYVSV, AY829113), espécies descritas infectando tomateiro no Brasil. A presença de begomovírus em pimentão foi verificada nas regiões de Alvinlândia, Ubirajara, Botucatu, Elias-Fausto, Paulínia, Mogi Guaçu, Paranapanema e Pirajú.
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No ano agrícola de 2000/2001, ocorreu um surto de nanismo e necrose da haste em soja (Glycine max) plantada em duas áreas do Brasil Central e na safra seguinte, esta anomalia foi constatada em outras regiões produtoras, mesmo distantes mais de 2.000 km de onde fora inicialmente constatada. Estudos envolvendo ensaios de transmissão (enxertia, mecânica e insetos vetores), microscopia eletrônica, purificação, sorologia e ensaios moleculares indicaram que a enfermidade foi causada por um carlavirus transmitido por mosca branca, possivelmente relacionado ao Cowpea mild mottle virus (CpMMV).
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
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Pós-graduação em Agronomia (Proteção de Plantas) - FCA
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
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Expression of antibodies in plant against essential viral proteins could provide an alternative approach to engineered viral resistance. Engineered single chain Fv antibodies scFV are particularly suitable for expression in plant because of their small size and the lack of assembly requirements. RNA-dependent RNA polymerases (RdRps) function as the catalytic subunit of viral replicases required for the replication of all positive strand RNA viruses. By using Phage technology we selected scFvs from a phage library using purified E.coli expressed TBSV(Tomato bushy stunt virus) replicase as antigen. The scFvs mediated-inhibition of RdRp activity was studied in vitro and in planta. In vitro experiments showed the inhibition of CNV(Cucumber necrosis virus) and TCV(Turnip crinkle virus) RdRp. Transient in planta assays based on agroinfiltration and an infectious clone of TBSV demonstrated the inhibition of the replication of TBSV(Tomato bushy stunt virus). Epitope mapping showed that the selected scFvs target the motif E of RdRp which is involved in template binding.Moreover T1 plants of transgenic lines of N. benthamiana expressing different scFvs either in the cytoplasm or the ER (endoplasmic reticulum) showed a high level of resistance against infection with TBSV and RCNMV(Red clover necrotic mosaic virus) upon inoculation with virus particles. This is the first report that scFvs against a RdRp of a plant viruses can inhibit viral replication in vivo. The resistance is even efficient against viruses belonging to different virus families.
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El tomate de cáscara (Physalis ixocarpa Brot.) es un cultivo alimenticio de gran importancia económica en México. Sin embargo, es afectado por diversas plagas y enfermedades tales como los Thrips (Thysanoptera: Frankliniella occidentalis) y el virus de la marchitez manchada del tomate (TSWV) que llegan a causar hasta un 80% de pérdidas. El objetivo del presente trabajo fue modelizar la distribución espacial de huevos de Thrips mediante técnicas geoestadísticas y obtener, en consecuencia, mapas de incidencia por medio del Kriging. Se georreferenciaron 121 puntos de muestreo en cada una de las parcelas comerciales de los municipios de Luvianos, Jocotitlán e Ixtlahuaca, a través del método de transectos en tres etapas fenológicas del cultivo. Se contabilizó el número de huevos de Thrips en cada punto de muestreo. Los resultados mostraron que las poblaciones de huevos deThrips presentan una distribución agregada, identificándose varios centros de conglomeración a través de los mapas obtenidos. Los semivariogramas obtenidos de la distribución espacial se ajustaron principalmente a los modelos gaussianos y esféricos. La distribución de huevos de Thrips se presentó en centros de agregación dentro de las parcelas estudiadas, lo cual permitirá establecer estrategias y medidas de control o mitigación en términos de sitios específicos de infestación de huevos de Thrips.
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Studies in Iowa have long documented the vulnerability of wells with less than 50 feet (15 meters) of confining materials above the source aquifer to contamination from nitrate and various pesticides. Recent studies in Wisconsin have documented the occurrence of viruses in untreated groundwater, even in wells considered to have little vulnerability to contamination from near-surface activities. In addition, sensitive methods have become available for analyses of pharmaceuticals and pesticides. This study represents the first comprehensive examination of contaminants of emerging concern in Iowa’s groundwater conducted to date, and one of the first conducted in the United States. Raw groundwater samples were collected from 66 public supply wells during the spring of 2013, when the state was recovering from drought conditions. Samples were analyzed for 206 chemical and biological parameters; including 20 general water-quality parameters and major ions, 19 metals, 5 nutrients, 10 virus groups, 3 species of pathogenic bacteria, 5 microbial indicators, 108 pharmaceuticals, 35 pesticides and pesticide degradates, and tritium. The wells chosen for this study represent a diverse range of ages, depths, confining material thicknesses, pumping rates, and land use settings. The most commonly detected contaminant group was pesticide compounds, which were present in 41% of the samples. As many as 6 pesticide compounds were found together in a sample, most of which were chloroacetanilide degradates. While none of the measured concentrations of pesticide compounds exceeded current benchmark levels, several of these compounds are listed on the U.S. Environmental Protection Agency’s Contaminant Candidate List and could be subject to drinking water standards in the future. Despite heavy use in the past decade, glyphosate was not detected, and its metabolite, aminomethylphosphonic acid, was only detected in two of 60 wells tested (3%) at the detection limit of 0.02 μg/L. Pharmaceutical compounds were detected in 35% of 63 samples. Of the 14 pharmaceuticals detected, six had reported concentrations above the method reporting limit, with the maximum reported concentration of 826 ng/L for acetaminophen. Diphenhydramine was the only pharmaceutical to have two detections above the reporting limit, at 24.5 and 145 ng/L. Eight pharmaceuticals had confirmed detections at concentrations below the method reporting limit. Caffeine was the most frequently detected pharmaceutical compound (25%), followed by the caffeine metabolite, 1,7-dimethylxanthine (16%). Microorganisms were detected in 21% of the wells using quantitative polymerase chain reaction methodologies. The most frequently detected microorganism was the pepper mild mottle virus (PMMV), a plant pathogen found in human waste. PMMV was detected in 17% of samples at concentrations ranging from 0.4 to 6.38 gene copies per liter. GII norovirus, human polyomavirus, bovine polyomavirus, and Campylobacter were also detected, while adenovirus, enterovirus, GI norovirus, swine hepatitis E, Salmonella, and enterohemmorhagic E. coli were not detected. No correlations were found between viruses or pathogenic bacteria and microbial indicators. Wells with less than 50 feet (15 meters) of confining material were shown to have greater incidence of surface-related contaminants; however, significant relationships (p<0.05) between confining layer thickness and contaminants were only found for nitrate and herbicides.
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Em 1998, Peanut mottle virus - PeMoV foi relatado em A. pintoi na Região de Cerrado, no Brasil. Plantas anormais com clorose, mosaico e mosqueado foram observadas em amendoim forrageiro (Arachis spp.) cultivado no campo, no Acre. Para entender a causa dessa anormalidade realizou-se um trabalho epidemiológico com diagnóstico e avaliação da reação de plantas em campo.
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Partial nucleotide sequences of five tomato infecting Begomovirus isolates were determined from DNA-A fragments, corresponding to the 5' region of the replication associated protein gene, the intergenic region and the 5' region of the coat protein gene. Isolate DFM shared 95% identity with Tomato mottle leaf curl virus (TMoLCV), isolates 34, PA-05, and Ta4 were 88% identical to Tomato yellow vein streak virus and isolate DF-BR3 shared 77% identity with TMoLCV. Recombination analysis indicated that isolate DF-BR3 was a chimaera, and it provided evidence that there is a complex and actively recombining population of tomato infecting begomoviruses in Brazil.
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The tomato cv. Fukuju nº. 2 was used for studying the effect of single and double infections with Potato virus X (PVX) and Tobacco mosaic virus (TMV). Mixed infection resulted in a synergistic increase of disease severity, where more growth reduction was seen with simultaneous inoculations than with sequential inoculations at four-day intervals. At five and 12 days post-inoculation, the increased severity of the disease coincided with enhancement of virus accumulation in the rapidly expanding upper leaves. The PVX concentration in leaves nº 5 to 7 of doubly infected plants was three to six fold that of singly infected ones, as determined by DAS-ELISA. Mixed infection with the L strain led to higher enhancement of PVX than with the TMV-L11A strain. The concentration of TMV-L was lower in double infection and significantly higher than TMV-L11A in both singly and doubly infected plants. Analyses of the PVX ORF2 by Western blot and Northern hybridization revealed the pattern of accumulation of the 25 kDa protein and the RNAs, respectively, following those of the virion and coat protein. The strain TMV-L11A overcame the resistance gene in cv. GCR 237 (Tm-1). In the upper leaf nº. 8, the concentration of PVX was three times higher in plants with mixed infection than with L11A. The concentrations of the L and OM (TMV strains) in both singly and doubly infected plants were at very low levels, and the synergistic effect on PVX concentration and disease severity was not observed.
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Um vírus isolado em Guaratinguetá, SP, de tomateiro (Lycoporsicon esculentum) 'Santa Clara' com sintomas característicos de virose, foi estudado por meio de plantas indicadoras e de hospedeiras diferenciais pertencentes a linhagens homozigotas de tomateiro, ensaios de estabilidade in vitro, purificação, contrastação negativa, testes sorológicos de ELISA-PTA e imunomicroscopia eletrônica, utilizando-se anti-soros contra diferentes vírus do gênero Tobamovirus. O isolado infetou plantas de espécies de amarantáceas, quenopodiáceas e solanáceas. Plantas de Chenopodium amaranticolor reagiram com sintomas locais e sistêmicos; Nicotiana sylvestris e N. rustica reagiram com lesões locais e a linhagem homozigota de tomateiro Tm-2 mostrou-se imune ao vírus. Nas preparações purificadas de contrastação negativa, foram observadas partículas rígidas e alongadas com cerca de 300 nm. O isolado foi identificado como um tobamovírus, com anti-soros contra o Tomato mosaic virus (ToMV) e Tobacco mosaic virus (TMV). As hospedeiras diferenciais indicaram se tratar de ToMV. Por meio de RT-PCR, com oligonucleotídeos para o gene da capa protéica de espécies do gênero Tobamovirus do subgrupo 1, amplificaram-se fragmentos com 850 pb que foram clonados e seqüenciados. A similaridade de nucleotídeos e aminoácidos deduzidos variou entre 85 e 91% quando a seqüência do ToMV-SP foi comparada com outras sequências de ToMV, 75 e 83% quando comparada com as do TMV e 67 e 72% quando comparada com a do Odontoglossum ringspot virus (ORSV). As comparações com outras espécies de tobamovírus apresentaram valores de similaridade inferiores a 65%. Confirmou-se a identidade dos vírus como sendo uma nova estirpe do ToMV.