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Registro Completo |
Biblioteca(s): |
Embrapa Arroz e Feijão; Embrapa Hortaliças. |
Data corrente: |
12/05/1997 |
Data da última atualização: |
12/05/1997 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
FARIA, J. C.; SOUZA-DIAS, J.A.C.; SLACK, S. A.; MAXWELL, D. P. |
Afiliação: |
EMBRAPA-CNPAF, Goiania, GO. |
Título: |
A new geminivirus associated with tomato in the State of Sao Paulo, Brazil. |
Ano de publicação: |
1997 |
Fonte/Imprenta: |
Plant Disease, v.81, n.4, p.423, 1997. |
Idioma: |
Inglês Português |
Notas: |
Notes. |
Conteúdo: |
The apical growth of about 20% of young tomato plants in observed fields near Campinas, State of São Paulo, Brazil, had yellow streaking of veins. Leaf symptoms developed into patches of yellow mosaic and the leaves became wavy. The whitefly Bemisia tabaci Genn. transmitted a pathogen from the infected tomato plants to healthy tomato and potato plants, reproducing the original symptoms in tomato. The apical leaves of infected potatoes showed yellow or green mottle that developed into leaf distortion with yellow blotches, symptoms indistinguishable from potato-deforming mosaic disease (2). DNA was extracted from these tomato and potato plants (1). Using DNA from the infected tomato plant, polymerase chain reaction (PCR) with the degenerate primer pair PAC1v1978/ PAV1c715 (1), which amplifies part of the rep gene (AC1 ORF), the common region (CR), and part of the cp gene (AV1 ORF), and with the primer pair PBC1v2039/PBV1c800, which amplifies part of BC1 ORF, CR, and part of BV1 ORF, gave virus-specific DNA fragments of the sizes expected from a whitefly-transmitted geminivirus. These were cloned and the complete nucleotide (sequences for DNA-A (pToYA, GenBank accession no. U79998) and DNA-B (pToYB, GenBank accession no. U80042) fragments obtained. Nucleotide identity between the CRs (184 nucleotides) was 90%, strongly indicating that those fragments correspond to a bipartite subgroup III geminivirus. PCR with the DNA from infected potato gave the expected size fragment for DNA-A. The partial sequence of the rep gene was 100% identical to the homologous sequence from the PCR fragment from the infected tomato. A search in the GenBank, EMBL, DDBJ, and PDB databases, using the BLAST program, found no identical geminivirus. The highest identity for the CR was 75% to tomato mottle geminivirus-Florida (ToMoV) and 74% to bean golden mosaic virus-Brazil. For the rep gene, the highest identity was 73% to tomato yellow leaf curl virus-Israel, an Old World geminivi-rus, followed by 71% to tomato golden mosaic virus-Brazil (TGMV) and ToMoV. For the cp gene, the highest identity was 86% to TGMV, followed by 83% to squash leaf curl geminivirus. Therefore, we propose the name tomato yellow vein streak geminivirus (ToYVSV) for this distinct virus (2). MenosThe apical growth of about 20% of young tomato plants in observed fields near Campinas, State of São Paulo, Brazil, had yellow streaking of veins. Leaf symptoms developed into patches of yellow mosaic and the leaves became wavy. The whitefly Bemisia tabaci Genn. transmitted a pathogen from the infected tomato plants to healthy tomato and potato plants, reproducing the original symptoms in tomato. The apical leaves of infected potatoes showed yellow or green mottle that developed into leaf distortion with yellow blotches, symptoms indistinguishable from potato-deforming mosaic disease (2). DNA was extracted from these tomato and potato plants (1). Using DNA from the infected tomato plant, polymerase chain reaction (PCR) with the degenerate primer pair PAC1v1978/ PAV1c715 (1), which amplifies part of the rep gene (AC1 ORF), the common region (CR), and part of the cp gene (AV1 ORF), and with the primer pair PBC1v2039/PBV1c800, which amplifies part of BC1 ORF, CR, and part of BV1 ORF, gave virus-specific DNA fragments of the sizes expected from a whitefly-transmitted geminivirus. These were cloned and the complete nucleotide (sequences for DNA-A (pToYA, GenBank accession no. U79998) and DNA-B (pToYB, GenBank accession no. U80042) fragments obtained. Nucleotide identity between the CRs (184 nucleotides) was 90%, strongly indicating that those fragments correspond to a bipartite subgroup III geminivirus. PCR with the DNA from infected potato gave the expected size fragment for DNA... Mostrar Tudo |
Palavras-Chave: |
Brasil; Diseases; Geminivirus; Ocorrencia; Ocurrence; São Paulo. |
Thesagro: |
Bemisia tabaci; Doença; Doença de planta; Lycopersicon Esculentum; Tomate; Vírus. |
Thesaurus Nal: |
Brazil; tomatoes. |
Categoria do assunto: |
-- H Saúde e Patologia |
Marc: |
LEADER 03106naa a2200337 a 4500 001 1757312 005 1997-05-12 008 1997 bl uuuu u00u1 u #d 100 1 $aFARIA, J. C. 245 $aA new geminivirus associated with tomato in the State of Sao Paulo, Brazil. 260 $c1997 500 $aNotes. 520 $aThe apical growth of about 20% of young tomato plants in observed fields near Campinas, State of São Paulo, Brazil, had yellow streaking of veins. Leaf symptoms developed into patches of yellow mosaic and the leaves became wavy. The whitefly Bemisia tabaci Genn. transmitted a pathogen from the infected tomato plants to healthy tomato and potato plants, reproducing the original symptoms in tomato. The apical leaves of infected potatoes showed yellow or green mottle that developed into leaf distortion with yellow blotches, symptoms indistinguishable from potato-deforming mosaic disease (2). DNA was extracted from these tomato and potato plants (1). Using DNA from the infected tomato plant, polymerase chain reaction (PCR) with the degenerate primer pair PAC1v1978/ PAV1c715 (1), which amplifies part of the rep gene (AC1 ORF), the common region (CR), and part of the cp gene (AV1 ORF), and with the primer pair PBC1v2039/PBV1c800, which amplifies part of BC1 ORF, CR, and part of BV1 ORF, gave virus-specific DNA fragments of the sizes expected from a whitefly-transmitted geminivirus. These were cloned and the complete nucleotide (sequences for DNA-A (pToYA, GenBank accession no. U79998) and DNA-B (pToYB, GenBank accession no. U80042) fragments obtained. Nucleotide identity between the CRs (184 nucleotides) was 90%, strongly indicating that those fragments correspond to a bipartite subgroup III geminivirus. PCR with the DNA from infected potato gave the expected size fragment for DNA-A. The partial sequence of the rep gene was 100% identical to the homologous sequence from the PCR fragment from the infected tomato. A search in the GenBank, EMBL, DDBJ, and PDB databases, using the BLAST program, found no identical geminivirus. The highest identity for the CR was 75% to tomato mottle geminivirus-Florida (ToMoV) and 74% to bean golden mosaic virus-Brazil. For the rep gene, the highest identity was 73% to tomato yellow leaf curl virus-Israel, an Old World geminivi-rus, followed by 71% to tomato golden mosaic virus-Brazil (TGMV) and ToMoV. For the cp gene, the highest identity was 86% to TGMV, followed by 83% to squash leaf curl geminivirus. Therefore, we propose the name tomato yellow vein streak geminivirus (ToYVSV) for this distinct virus (2). 650 $aBrazil 650 $atomatoes 650 $aBemisia tabaci 650 $aDoença 650 $aDoença de planta 650 $aLycopersicon Esculentum 650 $aTomate 650 $aVírus 653 $aBrasil 653 $aDiseases 653 $aGeminivirus 653 $aOcorrencia 653 $aOcurrence 653 $aSão Paulo 700 1 $aSOUZA-DIAS, J.A.C. 700 1 $aSLACK, S. A. 700 1 $aMAXWELL, D. P. 773 $tPlant Disease$gv.81, n.4, p.423, 1997.
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Registro original: |
Embrapa Hortaliças (CNPH) |
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Registro Completo
Biblioteca(s): |
Embrapa Semiárido. |
Data corrente: |
27/02/2008 |
Data da última atualização: |
29/07/2019 |
Tipo da produção científica: |
Resumo em Anais de Congresso |
Autoria: |
RIBAS, R. F.; MELO, R. F. de; OCHOA, M. A.; GODFOY, A. G. de; ALMEIDA, A. M. de; LOUREIRO, M. E.; OLIVA, M. A.; DIAS, L. E. |
Afiliação: |
Rogério Ferreira Ribas, UFV; ROSELI FREIRE DE MELO, CPATSA; Maite Arlegui Ochoa, Universidad Pública de Navarra Espanha; Alice Gontijo de Godoy, UFV; Andreia Miyasaka de Almeida, UFV; Marcelo Ehlers Loureiro, UFV; Marco Antonio Oliva, UFV; Luiz Eduardo Dias, UFV. |
Título: |
Respostas fotossinteticas de Sesbania exasperata Kunth cultivada na presença de arsênio. |
Ano de publicação: |
2007 |
Fonte/Imprenta: |
Brazilian Journal of Plant Physiology, Campinas, v. 19, 2007. |
Descrição Física: |
1 CD-ROM. |
Idioma: |
Português |
Notas: |
Suplemento. Edição dos Resumos do XI Congresso Brasileiro de Fisiologia Vegetal, Gramado, set. 2007. |
Conteúdo: |
Com objetivo de estudar os efeitos da toxicidade do As em plantas, avaliaram-se as respostas fotossintéticas de Sesbania exasperata cultivadas em vasos plásticos com 1,39 dm3 de solo nas concentrações de 0; 100; 200; 400 e 800 mg dm-3 de As, na forma de arsenato de sódio. |
Palavras-Chave: |
Arsênio; Fitotoxidez; Fluorescência. |
Thesagro: |
Fotossíntese; Planta. |
Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/CPATSA/37126/1/OPB1696.pdf
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Marc: |
LEADER 01150nam a2200277 a 4500 001 1160757 005 2019-07-29 008 2007 bl uuuu u00u1 u #d 100 1 $aRIBAS, R. F. 245 $aRespostas fotossinteticas de Sesbania exasperata Kunth cultivada na presença de arsênio.$h[electronic resource] 260 $aBrazilian Journal of Plant Physiology, Campinas, v. 19$c2007 300 $c1 CD-ROM. 500 $aSuplemento. Edição dos Resumos do XI Congresso Brasileiro de Fisiologia Vegetal, Gramado, set. 2007. 520 $aCom objetivo de estudar os efeitos da toxicidade do As em plantas, avaliaram-se as respostas fotossintéticas de Sesbania exasperata cultivadas em vasos plásticos com 1,39 dm3 de solo nas concentrações de 0; 100; 200; 400 e 800 mg dm-3 de As, na forma de arsenato de sódio. 650 $aFotossíntese 650 $aPlanta 653 $aArsênio 653 $aFitotoxidez 653 $aFluorescência 700 1 $aMELO, R. F. de 700 1 $aOCHOA, M. A. 700 1 $aGODFOY, A. G. de 700 1 $aALMEIDA, A. M. de 700 1 $aLOUREIRO, M. E. 700 1 $aOLIVA, M. A. 700 1 $aDIAS, L. E.
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