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Registro Completo |
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Biblioteca(s): |
Embrapa Mandioca e Fruticultura. |
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Data corrente: |
24/10/2006 |
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Data da última atualização: |
23/08/2023 |
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Autoria: |
REINHARDT, D. H. R. C.; SOUZA, L. F. da S.; CABRAL, J. R. S. (Org.). |
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Afiliação: |
DOMINGO HAROLDO RUDOLFO C REINHARDT, CNPMF; Luciano da Silva Souza, CNPMF; José Renato S. Cabral, CNPMF. |
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Título: |
Abacaxi produção: aspectos técnicos. |
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Ano de publicação: |
2000 |
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Fonte/Imprenta: |
Brasília, DF: Embrapa Informação Tecnológica; Cruz das Almas: Embrapa Mandioca e Fruticultura, 2000. |
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Páginas: |
77 p. |
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Série: |
( Frutas do Brasil, 7). |
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ISBN: |
85-7383-084-0 |
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Idioma: |
Português |
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Conteúdo: |
O abacaxizeiro é, provavelmente, originário da região compreendida entre 15°N e 30°S de latitude e 40°L e 60°W de longitude, o que inclui as zonas central e sul do Brasil, o nordeste da Argentina e o Paraguai. Estudos de distribuição do gênero Ananas indicam que o seu centro de origem é a região da Amazônia compreendida entre 10°N e 10°S de latitude e entre 55°L e 75°W de longitude, por se encontrar nela o maior número de espécies consideradas válidas até o momento. Assim, a região Norte do Brasil pode ser considerada um segundo centro de diversificação desse gênero.
Autores:SOUZA, A. da S.; MATOS, A.P.de; CARDOSO, C.E.L.; RITZINGER, C.H.S.P.; COSTA, D. da C.; REINHARDT, D.H.; CUNHA, G.A.P.da; SOUZA, J. da S.; CABRAL, J.R.S.; SOUZA, L.F.da S.; SANCHES, N.F.; ALMEIDA, O.A. de; MEISSNER FILHO, P.E. |
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Palavras-Chave: |
Pineapple. |
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Thesagro: |
Abacaxi. |
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Thesaurus Nal: |
Ananas. |
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Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
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Marc: |
LEADER 01427nam a2200205 a 4500
001 1652956
005 2023-08-23
008 2000 bl uuuu u0uu1 u #d
020 $a85-7383-084-0
100 1 $aREINHARDT, D. H. R. C.
245 $aAbacaxi produção$baspectos técnicos.
260 $aBrasília, DF: Embrapa Informação Tecnológica; Cruz das Almas: Embrapa Mandioca e Fruticultura$c2000
300 $a77 p.
490 $a( Frutas do Brasil, 7).
520 $aO abacaxizeiro é, provavelmente, originário da região compreendida entre 15°N e 30°S de latitude e 40°L e 60°W de longitude, o que inclui as zonas central e sul do Brasil, o nordeste da Argentina e o Paraguai. Estudos de distribuição do gênero Ananas indicam que o seu centro de origem é a região da Amazônia compreendida entre 10°N e 10°S de latitude e entre 55°L e 75°W de longitude, por se encontrar nela o maior número de espécies consideradas válidas até o momento. Assim, a região Norte do Brasil pode ser considerada um segundo centro de diversificação desse gênero. Autores:SOUZA, A. da S.; MATOS, A.P.de; CARDOSO, C.E.L.; RITZINGER, C.H.S.P.; COSTA, D. da C.; REINHARDT, D.H.; CUNHA, G.A.P.da; SOUZA, J. da S.; CABRAL, J.R.S.; SOUZA, L.F.da S.; SANCHES, N.F.; ALMEIDA, O.A. de; MEISSNER FILHO, P.E.
650 $aAnanas
650 $aAbacaxi
653 $aPineapple
700 1 $aSOUZA, L. F. da S.
700 1 $aCABRAL, J. R. S. (Org.)
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Registro original: |
Embrapa Mandioca e Fruticultura (CNPMF) |
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Voltar
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Registro Completo
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Biblioteca(s): |
Embrapa Café. |
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Data corrente: |
22/02/2011 |
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Data da última atualização: |
10/03/2011 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
A - 1 |
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Autoria: |
RAMIRO, D. A.; ESCOUTE, J.; PETITOT, A.-S.; NICOLE, M.; MALUF, M. P.; FERNANDEZ, D. |
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Afiliação: |
INSTITUTE DE RECHERCHE POUR LE DEVELOPPEMENT; CIRAD; INSTITUTE DE RECHERCHE POUR LE DEVELOPPEMENT; INSTITUTE DE RECHERCHE POUR LE DEVELOPPEMENT; MIRIAN PEREZ MALUF, SAPC; INSTITUTE DE RECHERCHE POUR LE DEVELOPPEMENT. |
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Título: |
Biphasic haustorial differentiation of coffee rust (Hemileia vastatrix race II) associated with defense responses in resistant and susceptible coffee cultivars. |
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Ano de publicação: |
2009 |
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Fonte/Imprenta: |
In.: PLANT PATHOLOGY, v. 58, p. 944-955, 2009. |
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Idioma: |
Inglês |
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Conteúdo: |
The objective of this study was to assess whether defence responses in coffee (Coffea arabica) were linked to a specific developmental stage of the rust fungus Hemileia vastatrix. Histological observations in compatible and incompatible highyielding Brazilian coffee cultivars showed that the fungus produced ?pioneer? haustoria in adjacent and subsidiary stomatal cells soon after entering the stomata, followed by later developed ?secondary haustoria? which invade mesophyll cells. In the incompatible interaction between Race II and cv. Tupi, a strong and transient H2O2 generation at infection sites was detected at 39 h post inoculation (hpi) during secondary haustoria formation. In addition, clear-cut differences in defence gene expression between compatible and incompatible interactions were only observed during the secondary haustoria formation. Transcripts of the pathogenesis-related (PR) genes CaPR1b and CaPR10 accumulated to maximal levels at 39 hpi (38- and 86-fold, respectively) in the incompatible interaction, but stayed at low levels in the compatible interaction. In contrast, the CaWRKY1 gene and the CaRLK gene were only induced in the susceptible cultivar. These results indicated that the specific resistance of cv. Tupi was expressed after differentiation of the H. vastatrix secondary haustoria. Analysis showed no evidence of specific recognition of coffee rust at the pioneer haustoria stage, suggesting that haustoria components are not recognized by, or not secreted into, the subsidiary and adjacent cells of the stomata. Additionally, the present study provides new insights into the colonization process of the coffee rust fungus. MenosThe objective of this study was to assess whether defence responses in coffee (Coffea arabica) were linked to a specific developmental stage of the rust fungus Hemileia vastatrix. Histological observations in compatible and incompatible highyielding Brazilian coffee cultivars showed that the fungus produced ?pioneer? haustoria in adjacent and subsidiary stomatal cells soon after entering the stomata, followed by later developed ?secondary haustoria? which invade mesophyll cells. In the incompatible interaction between Race II and cv. Tupi, a strong and transient H2O2 generation at infection sites was detected at 39 h post inoculation (hpi) during secondary haustoria formation. In addition, clear-cut differences in defence gene expression between compatible and incompatible interactions were only observed during the secondary haustoria formation. Transcripts of the pathogenesis-related (PR) genes CaPR1b and CaPR10 accumulated to maximal levels at 39 hpi (38- and 86-fold, respectively) in the incompatible interaction, but stayed at low levels in the compatible interaction. In contrast, the CaWRKY1 gene and the CaRLK gene were only induced in the susceptible cultivar. These results indicated that the specific resistance of cv. Tupi was expressed after differentiation of the H. vastatrix secondary haustoria. Analysis showed no evidence of specific recognition of coffee rust at the pioneer haustoria stage, suggesting that haustoria components are not recognized by, or not secrete... Mostrar Tudo |
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Palavras-Chave: |
Pathogenesis-related genes; Quantitative real-time PCR. |
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Thesagro: |
Coffea Arábica. |
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Thesaurus NAL: |
Reactive oxygen species. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/29268/1/Biphasic-haustorial.pdf
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Marc: |
LEADER 02423naa a2200229 a 4500
001 1880368
005 2011-03-10
008 2009 bl uuuu u00u1 u #d
100 1 $aRAMIRO, D. A.
245 $aBiphasic haustorial differentiation of coffee rust (Hemileia vastatrix race II) associated with defense responses in resistant and susceptible coffee cultivars.$h[electronic resource]
260 $c2009
520 $aThe objective of this study was to assess whether defence responses in coffee (Coffea arabica) were linked to a specific developmental stage of the rust fungus Hemileia vastatrix. Histological observations in compatible and incompatible highyielding Brazilian coffee cultivars showed that the fungus produced ?pioneer? haustoria in adjacent and subsidiary stomatal cells soon after entering the stomata, followed by later developed ?secondary haustoria? which invade mesophyll cells. In the incompatible interaction between Race II and cv. Tupi, a strong and transient H2O2 generation at infection sites was detected at 39 h post inoculation (hpi) during secondary haustoria formation. In addition, clear-cut differences in defence gene expression between compatible and incompatible interactions were only observed during the secondary haustoria formation. Transcripts of the pathogenesis-related (PR) genes CaPR1b and CaPR10 accumulated to maximal levels at 39 hpi (38- and 86-fold, respectively) in the incompatible interaction, but stayed at low levels in the compatible interaction. In contrast, the CaWRKY1 gene and the CaRLK gene were only induced in the susceptible cultivar. These results indicated that the specific resistance of cv. Tupi was expressed after differentiation of the H. vastatrix secondary haustoria. Analysis showed no evidence of specific recognition of coffee rust at the pioneer haustoria stage, suggesting that haustoria components are not recognized by, or not secreted into, the subsidiary and adjacent cells of the stomata. Additionally, the present study provides new insights into the colonization process of the coffee rust fungus.
650 $aReactive oxygen species
650 $aCoffea Arábica
653 $aPathogenesis-related genes
653 $aQuantitative real-time PCR
700 1 $aESCOUTE, J.
700 1 $aPETITOT, A.-S.
700 1 $aNICOLE, M.
700 1 $aMALUF, M. P.
700 1 $aFERNANDEZ, D.
773 $tIn.: PLANT PATHOLOGY$gv. 58, p. 944-955, 2009.
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Registro original: |
Embrapa Café (CNPCa) |
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