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Registro Completo |
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Biblioteca(s): |
Embrapa Cerrados; Embrapa Unidades Centrais. |
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Data corrente: |
02/07/2015 |
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Data da última atualização: |
20/08/2015 |
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Tipo da produção científica: |
Documentos |
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Autoria: |
FALEIRO, F. G.; JUNQUEIRA, N. T. V.; OLIVEIRA, E. J. de; MACHADO, C. de F.; PEIXOTO, J. R.; COSTA, A. M.; GUIMARAES, T. G.; JUNQUEIRA, K. P. |
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Afiliação: |
FABIO GELAPE FALEIRO, CPAC; NILTON TADEU VILELA JUNQUEIRA, CPAC; EDER JORGE DE OLIVEIRA, CNPMF; CRISTINA DE FATIMA MACHADO, CNPMF; JOSÉ RICARDO PEIXOTO, UNB; ANA MARIA COSTA, CPAC; TADEU GRACIOLLI GUIMARAES, CPAC; KEIZE PEREIRA JUNQUEIRA, SPM GGE. |
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Título: |
Caracterização de germoplasma e melhoramento genético do maracujazeiro assistidos por marcadores moleculares - fase 2: resultados de pesquisa 2008-2012. |
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Ano de publicação: |
2014 |
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Fonte/Imprenta: |
Planaltina, DF: Embrapa Cerrados, 2014. |
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Páginas: |
102 p. |
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Série: |
(Embrapa Cerrados. Documentos, 324). |
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Idioma: |
Português |
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Conteúdo: |
São apresentados os principais resultados obtidos na fase II do projeto que foi executado de 2008 a 2012, em conjunto com os resultados do projeto Melhoramento genético do maracujazeiro (Passiflora spp.) visando sua utilização diversificfada e valoração da biodiversidade essencialmente brasileira, financiado pelo CNPq. Na apresentação dos resultados, foram enfocados o cumprimento de objetivos e metas a geração de publicações técnico-científicas, o desenvolvimento de produtos tecnológicos e diferentes ações de transferência de tecnologia. Destaque especial foi a validação do desempenho agronômico dos híbridos de maracujazeiro-azedo BRS Sol do Cerrado, BRS Gigante Amarelo e BRS Ouro Vermelho em várias regiões do Brasil e o lançamento da cultivar de maracajuzeiro-azedo BRS Rubi do Cerrado em 2012. |
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Palavras-Chave: |
Cultivar evaluation; Lançamento de variedade; Molecular markers; Passion fruit. |
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Thesagro: |
Maracujá; Passiflora edulis; Recurso Genético; Transferência de Tecnologia. |
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Thesaurus Nal: |
plant breeding. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/128192/1/doc-324.pdf
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Marc: |
LEADER 01845nam a2200325 a 4500
001 2019176
005 2015-08-20
008 2014 bl uuuu 00u1 u #d
100 1 $aFALEIRO, F. G.
245 $aCaracterização de germoplasma e melhoramento genético do maracujazeiro assistidos por marcadores moleculares - fase 2$bresultados de pesquisa 2008-2012.
260 $aPlanaltina, DF: Embrapa Cerrados$c2014
300 $a102 p.
490 $a(Embrapa Cerrados. Documentos, 324).
520 $aSão apresentados os principais resultados obtidos na fase II do projeto que foi executado de 2008 a 2012, em conjunto com os resultados do projeto Melhoramento genético do maracujazeiro (Passiflora spp.) visando sua utilização diversificfada e valoração da biodiversidade essencialmente brasileira, financiado pelo CNPq. Na apresentação dos resultados, foram enfocados o cumprimento de objetivos e metas a geração de publicações técnico-científicas, o desenvolvimento de produtos tecnológicos e diferentes ações de transferência de tecnologia. Destaque especial foi a validação do desempenho agronômico dos híbridos de maracujazeiro-azedo BRS Sol do Cerrado, BRS Gigante Amarelo e BRS Ouro Vermelho em várias regiões do Brasil e o lançamento da cultivar de maracajuzeiro-azedo BRS Rubi do Cerrado em 2012.
650 $aplant breeding
650 $aMaracujá
650 $aPassiflora edulis
650 $aRecurso Genético
650 $aTransferência de Tecnologia
653 $aCultivar evaluation
653 $aLançamento de variedade
653 $aMolecular markers
653 $aPassion fruit
700 1 $aJUNQUEIRA, N. T. V.
700 1 $aOLIVEIRA, E. J. de
700 1 $aMACHADO, C. de F.
700 1 $aPEIXOTO, J. R.
700 1 $aCOSTA, A. M.
700 1 $aGUIMARAES, T. G.
700 1 $aJUNQUEIRA, K. P.
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Registro original: |
Embrapa Cerrados (CPAC) |
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Biblioteca |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Hortaliças. Para informações adicionais entre em contato com cnph.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Agricultura Digital; Embrapa Hortaliças. |
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Data corrente: |
09/08/2022 |
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Data da última atualização: |
11/08/2022 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
B - 1 |
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Autoria: |
MARTINS, T. P.; REGO, C. M.; NAKASU, E. Y. T.; FERNANDES, F. R.; INOUE-NAGATA, A. K. |
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Afiliação: |
T. P. MARTINS, UNIVERSIDADE DE BRASÍLIA; C. M. REGO, UNIVERSIDADE DE BRASÍLIA; ERICH YUKIO TEMPEL NAKASU, CNPH; FERNANDA RAUSCH FERNANDES, CNPTIA; ALICE KAZUKO INOUE NAGATA, CNPH. |
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Título: |
A high viral diversity in tomato crops in Brazil is revealed by next generation sequencing analyses. |
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Ano de publicação: |
2021 |
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Fonte/Imprenta: |
Acta Horticulturae, v. 1316, p. 99-105, 2021. |
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ISSN: |
2406-6168 |
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DOI: |
10.17660/ActaHortic.2021.1316.14 |
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Idioma: |
Inglês |
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Notas: |
Edition of Proceedings of the VI International Symposium on Tomato Diseases: Managing Tomato Diseases in the Face of Globalization and Climate Change. |
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Conteúdo: |
Tomato is planted in Brazil mainly for fresh consumption and tomato paste production. Among the various pathogens that infect tomato plants in Brazil, viruses are particularly important due to their high incidence and the resulting losses caused. Diagnosis of viral diseases usually relies on detection methods directed to known viruses and close variants, either by serology or nucleic acid hybridization/ amplification. However, the advent of next generation sequencing (NGS) facilitated a deep analysis of viral populations, which can be used for identification, assembly and discovery of new viruses. Aiming to estimate the viral diversity present in tomato crops from three states of Brazil, five composite leaf samples were analyzed using NGS. The samples referred as Braz (collected in the Federal District, 2015); Ahol, Toca1, and Toca2 (São Paulo State, 2014), and RNY2 (Minas Gerais State, 2013) were submitted to semi-purification of viral particles and RNA extraction before RNA-seq (Illumina). The reads were filtered for quality, the contigs assembled (Velvet algorithm), and submitted to MegaBLAST analysis against a virus reference sequences database. These samples were collected from plants showing symptoms such as mosaic, chlorosis, leaf curling, chlorotic spots, necrosis and stunting. Known viruses belonging to nine genera, Crinivirus, Begomovirus, Tospovirus, Tobravirus, Potyvirus, Tobamovirus, Tymovirus, Potexvirus and Cucumovirus, were detected. Potentially undescribed and unreported viruses in tomatoes, such as an amalgavirus and an ilarvirus, were also detected and are under confirmation. The conclusion was that there is a high virus diversity present in tomato plants in Brazil, making tomato production a challenge to the growers. The crinivirus, Tomato chlorosis virus, was the most frequently found within the samplings, suggesting that it is widespread in the major tomato production areas. Two begomoviruses were detected, implying that this strategy is also useful to detect viruses with a DNA genome. Finally, this technique was particularly convenient to identify the viruses coexisting in tomatoes and to find unknown viruses that may threaten the tomato production in the country. MenosTomato is planted in Brazil mainly for fresh consumption and tomato paste production. Among the various pathogens that infect tomato plants in Brazil, viruses are particularly important due to their high incidence and the resulting losses caused. Diagnosis of viral diseases usually relies on detection methods directed to known viruses and close variants, either by serology or nucleic acid hybridization/ amplification. However, the advent of next generation sequencing (NGS) facilitated a deep analysis of viral populations, which can be used for identification, assembly and discovery of new viruses. Aiming to estimate the viral diversity present in tomato crops from three states of Brazil, five composite leaf samples were analyzed using NGS. The samples referred as Braz (collected in the Federal District, 2015); Ahol, Toca1, and Toca2 (São Paulo State, 2014), and RNY2 (Minas Gerais State, 2013) were submitted to semi-purification of viral particles and RNA extraction before RNA-seq (Illumina). The reads were filtered for quality, the contigs assembled (Velvet algorithm), and submitted to MegaBLAST analysis against a virus reference sequences database. These samples were collected from plants showing symptoms such as mosaic, chlorosis, leaf curling, chlorotic spots, necrosis and stunting. Known viruses belonging to nine genera, Crinivirus, Begomovirus, Tospovirus, Tobravirus, Potyvirus, Tobamovirus, Tymovirus, Potexvirus and Cucumovirus, were detected. Potentially undescribed a... Mostrar Tudo |
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Palavras-Chave: |
HTS; Next Generation Sequencing; Sequenciamento de nova geração; Virome. |
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Thesagro: |
Tomate; Vírus. |
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Thesaurus NAL: |
Solanum lycopersicum. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 03214naa a2200289 a 4500
001 2145363
005 2022-08-11
008 2021 bl uuuu u00u1 u #d
022 $a2406-6168
024 7 $a10.17660/ActaHortic.2021.1316.14$2DOI
100 1 $aMARTINS, T. P.
245 $aA high viral diversity in tomato crops in Brazil is revealed by next generation sequencing analyses.$h[electronic resource]
260 $c2021
500 $aEdition of Proceedings of the VI International Symposium on Tomato Diseases: Managing Tomato Diseases in the Face of Globalization and Climate Change.
520 $aTomato is planted in Brazil mainly for fresh consumption and tomato paste production. Among the various pathogens that infect tomato plants in Brazil, viruses are particularly important due to their high incidence and the resulting losses caused. Diagnosis of viral diseases usually relies on detection methods directed to known viruses and close variants, either by serology or nucleic acid hybridization/ amplification. However, the advent of next generation sequencing (NGS) facilitated a deep analysis of viral populations, which can be used for identification, assembly and discovery of new viruses. Aiming to estimate the viral diversity present in tomato crops from three states of Brazil, five composite leaf samples were analyzed using NGS. The samples referred as Braz (collected in the Federal District, 2015); Ahol, Toca1, and Toca2 (São Paulo State, 2014), and RNY2 (Minas Gerais State, 2013) were submitted to semi-purification of viral particles and RNA extraction before RNA-seq (Illumina). The reads were filtered for quality, the contigs assembled (Velvet algorithm), and submitted to MegaBLAST analysis against a virus reference sequences database. These samples were collected from plants showing symptoms such as mosaic, chlorosis, leaf curling, chlorotic spots, necrosis and stunting. Known viruses belonging to nine genera, Crinivirus, Begomovirus, Tospovirus, Tobravirus, Potyvirus, Tobamovirus, Tymovirus, Potexvirus and Cucumovirus, were detected. Potentially undescribed and unreported viruses in tomatoes, such as an amalgavirus and an ilarvirus, were also detected and are under confirmation. The conclusion was that there is a high virus diversity present in tomato plants in Brazil, making tomato production a challenge to the growers. The crinivirus, Tomato chlorosis virus, was the most frequently found within the samplings, suggesting that it is widespread in the major tomato production areas. Two begomoviruses were detected, implying that this strategy is also useful to detect viruses with a DNA genome. Finally, this technique was particularly convenient to identify the viruses coexisting in tomatoes and to find unknown viruses that may threaten the tomato production in the country.
650 $aSolanum lycopersicum
650 $aTomate
650 $aVírus
653 $aHTS
653 $aNext Generation Sequencing
653 $aSequenciamento de nova geração
653 $aVirome
700 1 $aREGO, C. M.
700 1 $aNAKASU, E. Y. T.
700 1 $aFERNANDES, F. R.
700 1 $aINOUE-NAGATA, A. K.
773 $tActa Horticulturae$gv. 1316, p. 99-105, 2021.
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