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| Registros recuperados : 190 | |
| 62. |  | CARDOSO, P. C.; RANGEL, M. A. S.; TEIXEIRA, M. do R. de O. Desempenho de genótipos de soja em três épocas de semeadura, na safra 2004/05, em Aral Moreira, MS. In: REUNIÃO DE PESQUISA DE SOJA DA REGIÃO CENTRAL DO BRASIL, 27., 2005. Cornélio Procópio. Resumos... Londrina: Embrapa Soja, 2005. p. 56-58 (Embrapa Soja. Documentos, 257). Organizado por Odilon Ferreira Saraiva, Janete Lasso Ortiz, Simone Ery Grosskopf.| Biblioteca(s): Embrapa Agropecuária Oeste. |
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| 65. | | RANGEL, M. A. S.; RINGENBERG, R.; LEONEL, M.; FERNANDES, A. M.; SANTOS, V. da S. Propriedade de pasta do amido extraído de diferentes clones de mandioca e épocas de colheita. In: CIENTÍFICA EMBRAPA MANDIOCA E FRUTICULTURA, 15., 2021. Mulheres na ciência desafios, oportunidades e conquistas. Cruz das Almas, BA: Embrapa Mandioca e Fruticultura, 2021. 109 f. il. PDF.| Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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| 66. | | MINUZZI, A.; RANGEL, M. A. S.; BRACCINI, A. L.; SVAPIM, C. A.; MORA, F. Rendimento e características agronômicas de cultivares de soja colhidas em quatro épocas e dois ambientes do Estado de Mato Grosso do Sul. In: CONGRESSO BRASILEIRO DE SOJA, 4., 2006, Londrina. Resumos... Londrina: Embrapa Soja, 2006. p. 124. Organizado por Odilon Ferreira Saraiva, Simone Ery Grosskopf. p. 188| Biblioteca(s): Embrapa Agropecuária Oeste. |
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| 67. | | MINUZZI, A.; RANGEL, M. A. S.; BRACCINI, A. L.; SCAPIM, C. A.; MORA, F. Qualidade fisiológica e sanitária, teores de óleo e de proteínas nas sementes de cultivares de soja produzidas em dois ambientes e colhidas em quatro épocas no Estado do Mato Grosso do Sul. In: CONGRESSO BRASILEIRO DE SOJA, 4., 2006, Londrina. Resumos... Londrina: Embrapa Soja, 2006. p. 124. Organizado por Odilon Ferreira Saraiva, Simone Ery Grosskopf. p. 187| Biblioteca(s): Embrapa Agropecuária Oeste. |
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| 72. | | TEIXEIRA, M. do R. de O.; ALMEIDA, L. A. de; KIIHL, R. A. de S.; RANGEL, M. A. S. Comportamento da cultivar de soja BRS 134 na regiao sul de Mato Grosso do Sul. In: REUNIAO DE PESQUISA DE SOJA DA REGIAO CENTRAL DO BRASIL, 22., 2000, Cuiaba, MT. Resumos. Cuiaba: Embrapa Soja, 2000. p.44. (Embrapa Soja. Documentos, 144).| Biblioteca(s): Embrapa Cerrados. |
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| 77. | | ONO, F. B.; MONTAGNA, J.; SERAFIM, M. E.; NOVELINO, J. O.; DALLASTA, D. C.; RANGEL, M. A. S.; CREMON, C. Componentes de produção da soja influenciados por fontes e doses de fertilizantes fosfatados. In: CONGRESSO BRASILEIRO DE CIÊNCIA DO SOLO, 31., 2007, Gramado. Conquistas e desafios da ciência do solo brasileira. Porto Alegre: SBCS, 2007.| Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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| 78. | | VENTUROSO, L. R.; RANGEL, M. A. S.; SOUZA, F. R.; BERGAMIN, A. C.; CONUS, L. A.; COLETA, Q. P. Influência de diferentes níveis de mancha púrpura no vigor de sementes de soja. Fitopatologia Brasileira, Brasília, DF, v. 32, p. 161, ago. 2007. Suplemento. Edição dos Resumos do XL Congresso Brasiliero de Fitopatologia, Maringá, ago. 2007.| Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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| 79. | | COLETA, Q. P.; RANGEL, M. A. S.; SOUZA, F. R.; VENTUROSO, L. R.; CONUS, L. A.; POLIZEL, A. C. Avaliação de extratos vegetais e de fungicida no armazenamento de sementes de soja. Fitopatologia Brasileira, Brasília, DF, v. 32, p. 222, ago. 2007.Suplemento. Edição dos Resumos do XL Congresso Brasiliero de Fitopatologia, Maringá, ago. 2007.| Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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| 80. | | RANGEL, M. A. S.; MINUZZI, A.; BRACCINI, A. de L. e; SCAPIM, C. A.; CARDOSO, P. C. Efeito da interação genótipo x ambiente e da interação no rendimento de grãos e nos teores de proteína de cultivares de soja. Acta Scientiarum Agronomy, Maringá, v. 29, n. 3, p. 351-354, 2007| Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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| Registros recuperados : 190 | |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Mandioca e Fruticultura. Para informações adicionais entre em contato com cnpmf.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Mandioca e Fruticultura. |
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Data corrente: |
30/03/2009 |
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Data da última atualização: |
30/06/2023 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
KITAJIMA, E. W.; CALEGARIO, R. F.; NOVELLI, V. M.; LOCALI-FABRIS, E. C.; BASTIANEL, M.; FRANCISCHINI, F.; FREITAS-ASTUA, J. |
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Afiliação: |
Elliot Watanabe Kitajima, ESALQ; R. F. Calegario, ESALQ; Valdenice Moreira Novelli, APTA; Eliane Cristina Locali-Fabris, APTA; Marinês Bastianel, APTA; F. Francischini, Alellyx Genomics; Juliana Freitas-Ástua, CNPMF. |
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Título: |
In situ detection and immunolocalization of the Citrus leprosis virus cytoplasmic type (CiLV) in the mite vector and evidences that the virus/vector relationship is of circulative type. |
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Ano de publicação: |
2008 |
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Fonte/Imprenta: |
In: INTERNATIONAL SCIENTIFIC SEMINAR ON PLANT HEALTH, 6.; LATIN AMERICAN AND CARIBBEAN SYMPOSIUM, 2., 2008, La Habana, Cuba. Acarina Biodiversity: their use, protection and conservation. Havana, [s.n.], 2008. |
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Descrição Física: |
1 CD ROM |
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Idioma: |
Inglês |
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Conteúdo: |
Among the Brevipalpus (Acari: Tenuipalpidae)-transmitted plant viruses (BTV), citrus leprosis, cytoplasmic type (CiLV-C) is, by far, the most important. It causes localized lesions on the leaves, stems, and fruits and untreated plants may die within few years. Progresses have been made on the nature of CiLV-C. Infection by the virus induces a characteristic eletron dense and vacuolated inclusion (viroplasm) in the cytoplasm and the occurence of short, bacilliform virions of CiLV-C within endoplasmic reticulum. Its genome was completely sequenced being a bipartite (6 and 9 kb) positive sense ssRNA with a poly-A tail, different from other known viruses and a new genus Cilevirus was proposed for CiLV-C. Primers were designed for specific detection of CiLV-C and some of the viral proteins were expressed in vitro, including nucleocapsid (NC) protein and a specific antibody is available. The precise relationship between CiLV-C and its vector B. phoenicis has remained unclear. Recent works permitted to detect CiLV-C in the mite by RT - PCR and RT -qPCR assays suggest that the virus does not replicate in the mite. Transmission assays revealing that larvae and nymphs are also able to transmit CiLV-C are considered additional evidences for the absence of replication of the virus in the mite. Transmission electron microscopy of sections of viruliferous B. phoenicis allowed the visualization of virus-like particles as seen in the plant cells, in the mite bodies. they consistently occurred between membranes of adjacent cells near the midgut and prosomal gland. Anti-NC antibodies specifically labeled these particles both in the plant and in the mite thus confirming their viral nature. Viroplasmas, present in infected plant cells, are also immunolabeled by anti-NC antibody, but they were not found in the mite tissues. A possible mechanism to explain the viral presence between cells, similar to diapedesis of the leucocytes in blood vessels, is being suggested. These cytological evidences in the mite reinforce the concept that the CiLV-C/Brevipalpus relation is of circulative rather than replicative type. This information is relevant for epidemiology and control strategies. MenosAmong the Brevipalpus (Acari: Tenuipalpidae)-transmitted plant viruses (BTV), citrus leprosis, cytoplasmic type (CiLV-C) is, by far, the most important. It causes localized lesions on the leaves, stems, and fruits and untreated plants may die within few years. Progresses have been made on the nature of CiLV-C. Infection by the virus induces a characteristic eletron dense and vacuolated inclusion (viroplasm) in the cytoplasm and the occurence of short, bacilliform virions of CiLV-C within endoplasmic reticulum. Its genome was completely sequenced being a bipartite (6 and 9 kb) positive sense ssRNA with a poly-A tail, different from other known viruses and a new genus Cilevirus was proposed for CiLV-C. Primers were designed for specific detection of CiLV-C and some of the viral proteins were expressed in vitro, including nucleocapsid (NC) protein and a specific antibody is available. The precise relationship between CiLV-C and its vector B. phoenicis has remained unclear. Recent works permitted to detect CiLV-C in the mite by RT - PCR and RT -qPCR assays suggest that the virus does not replicate in the mite. Transmission assays revealing that larvae and nymphs are also able to transmit CiLV-C are considered additional evidences for the absence of replication of the virus in the mite. Transmission electron microscopy of sections of viruliferous B. phoenicis allowed the visualization of virus-like particles as seen in the plant cells, in the mite bodies. they consistently occurr... Mostrar Tudo |
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Thesagro: |
Ácaro; Vírus. |
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Categoria do assunto: |
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Marc: |
LEADER 03084nam a2200217 a 4500
001 1655634
005 2023-06-30
008 2008 bl uuuu u00u1 u #d
100 1 $aKITAJIMA, E. W.
245 $aIn situ detection and immunolocalization of the Citrus leprosis virus cytoplasmic type (CiLV) in the mite vector and evidences that the virus/vector relationship is of circulative type.$h[electronic resource]
260 $aIn: INTERNATIONAL SCIENTIFIC SEMINAR ON PLANT HEALTH, 6.; LATIN AMERICAN AND CARIBBEAN SYMPOSIUM, 2., 2008, La Habana, Cuba. Acarina Biodiversity: their use, protection and conservation. Havana, [s.n.]$c2008
300 $c1 CD ROM
520 $aAmong the Brevipalpus (Acari: Tenuipalpidae)-transmitted plant viruses (BTV), citrus leprosis, cytoplasmic type (CiLV-C) is, by far, the most important. It causes localized lesions on the leaves, stems, and fruits and untreated plants may die within few years. Progresses have been made on the nature of CiLV-C. Infection by the virus induces a characteristic eletron dense and vacuolated inclusion (viroplasm) in the cytoplasm and the occurence of short, bacilliform virions of CiLV-C within endoplasmic reticulum. Its genome was completely sequenced being a bipartite (6 and 9 kb) positive sense ssRNA with a poly-A tail, different from other known viruses and a new genus Cilevirus was proposed for CiLV-C. Primers were designed for specific detection of CiLV-C and some of the viral proteins were expressed in vitro, including nucleocapsid (NC) protein and a specific antibody is available. The precise relationship between CiLV-C and its vector B. phoenicis has remained unclear. Recent works permitted to detect CiLV-C in the mite by RT - PCR and RT -qPCR assays suggest that the virus does not replicate in the mite. Transmission assays revealing that larvae and nymphs are also able to transmit CiLV-C are considered additional evidences for the absence of replication of the virus in the mite. Transmission electron microscopy of sections of viruliferous B. phoenicis allowed the visualization of virus-like particles as seen in the plant cells, in the mite bodies. they consistently occurred between membranes of adjacent cells near the midgut and prosomal gland. Anti-NC antibodies specifically labeled these particles both in the plant and in the mite thus confirming their viral nature. Viroplasmas, present in infected plant cells, are also immunolabeled by anti-NC antibody, but they were not found in the mite tissues. A possible mechanism to explain the viral presence between cells, similar to diapedesis of the leucocytes in blood vessels, is being suggested. These cytological evidences in the mite reinforce the concept that the CiLV-C/Brevipalpus relation is of circulative rather than replicative type. This information is relevant for epidemiology and control strategies.
650 $aÁcaro
650 $aVírus
700 1 $aCALEGARIO, R. F.
700 1 $aNOVELLI, V. M.
700 1 $aLOCALI-FABRIS, E. C.
700 1 $aBASTIANEL, M.
700 1 $aFRANCISCHINI, F.
700 1 $aFREITAS-ASTUA, J.
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