Preservação, caracterização patogênica e molecular de Plasmodiophora brassicae, agente causal da hérnia das crucíferas
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Data
2007-12-18
Autores
Cruz, Juliana Cristina Sodário [UNESP]
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Editor
Universidade Estadual Paulista (Unesp)
Resumo
A doença conhecida por hérnia das crucíferas é causada pelo patógeno Plasmodiophora brassicae Woronin, sendo uma das mais importantes e de difícil controle em brássicas. Em virtude da dificuldade de preservação das estruturas de resistência de P. brassicae em condições laboratoriais, por se tratar de um parasita obrigatório, foi desenvolvido um ensaio visando a obtenção de uma técnica eficiente e prática de preservação. Para isto, raízes de diferentes brássicas naturalmente infectadas por P. brassicae, contendo hérnias, foram coletadas de uma mesma propriedade (município de Pardinho - SP), em diferentes períodos, e imediatamente congeladas em freezer a -20°C±2°C. Os tratamentos foram: T1: hérnias congeladas por 389 dias, (rúcula); T2: hérnias congeladas por 242 dias (brócolis); T3: hérnias congeladas por 21 dias (couve-chinesa) e T4: testemunha (sem inóculo). Os testes de patogenicidade, após os diferentes períodos de armazenamento, foram realizados em condições controladas de casa de vegetação (25±2°C), onde em cada planta, de uma variedade suscetível de couve-chinesa (Pak choi), foi inoculado 2mL da suspensão de esporos, dos diferentes tratamentos, na concentração de 107 esporos.mL–1. Cada tratamento contou com seis repetições distribuídas ao acaso. Passadas cinco semanas, após a inoculação, as raízes foram lavadas e avaliadas. Houve diferença estatística significativa entre os materiais avaliados quanto aos diferentes períodos de armazenamento em “freezer”. Os materiais congelados entre 21 a 242 dias preservaram suas características infectivas, sendo este método uma boa opção para a preservação das estruturas de repouso nesse período. Foram realizados testes de patogenicidade e análises moleculares de populações de P. brassicae,...
Disease known as clubroot of crucifers is caused by the pathogen Plasmodiophora brassicae Woronin, and is one of the most important and difficult control crucifer diseases in brassicas. Because of the difficulty in preserving the resistance structures of P. brassicae under laboratory conditions, given that it is an obligate parasite, an assay was carried out to develop a practical and effective technique that would allow further studies to be conducted. On this proposal, roots of different brassica species naturally infected by P. brassicae showing clubroot symptoms were collected in the some grower (Pardinho, SP-city, Brazil) during different seasons, and were immediately frozen at approximately 20°C±2°C. The treatments were: T1: clubroots frozen for 389 days (arugula); T2: clubroots frozen for 242 days (broccoli); T3: clubroots frozen for 21 days (Chinese cabbage), and T4: control (no inoculum). The pathogenicity tests after different storage periods were conducted under controlled greenhouse conditions (25±2°C); each plant of a susceptible variety of Chinese cabbage was inoculated with 2mL of a spore suspension of the various treatments at a concentration of 107spores.mL-1. Each treatment consisted of six replicates distributed at random. The roots were washed and evaluated five weeks after inoculation. There were statistical differences between the materials evaluated with respect to different storage periods in the freezer. Materials kept frozen between 21 and 242 days retained their infective traits. Therefore, this method is a good option to preserve resting spores during this period. In addition, pathogenicity tests and molecular analyses were conducted with P. brassicae populations obtained from infected roots of several production regions of Brazil, on some...(Complete abstract click electronic access below)
Disease known as clubroot of crucifers is caused by the pathogen Plasmodiophora brassicae Woronin, and is one of the most important and difficult control crucifer diseases in brassicas. Because of the difficulty in preserving the resistance structures of P. brassicae under laboratory conditions, given that it is an obligate parasite, an assay was carried out to develop a practical and effective technique that would allow further studies to be conducted. On this proposal, roots of different brassica species naturally infected by P. brassicae showing clubroot symptoms were collected in the some grower (Pardinho, SP-city, Brazil) during different seasons, and were immediately frozen at approximately 20°C±2°C. The treatments were: T1: clubroots frozen for 389 days (arugula); T2: clubroots frozen for 242 days (broccoli); T3: clubroots frozen for 21 days (Chinese cabbage), and T4: control (no inoculum). The pathogenicity tests after different storage periods were conducted under controlled greenhouse conditions (25±2°C); each plant of a susceptible variety of Chinese cabbage was inoculated with 2mL of a spore suspension of the various treatments at a concentration of 107spores.mL-1. Each treatment consisted of six replicates distributed at random. The roots were washed and evaluated five weeks after inoculation. There were statistical differences between the materials evaluated with respect to different storage periods in the freezer. Materials kept frozen between 21 and 242 days retained their infective traits. Therefore, this method is a good option to preserve resting spores during this period. In addition, pathogenicity tests and molecular analyses were conducted with P. brassicae populations obtained from infected roots of several production regions of Brazil, on some...(Complete abstract click electronic access below)
Descrição
Palavras-chave
Patogenicidade, Genetica molecular, Brassica, Plasmodiophora Brasssicae, Soilborne pathogen, Brassicaceae, Pathogenicity, Genetic traits
Como citar
CRUZ, Juliana Cristina Sodário. Preservação, caracterização patogênica e molecular de Plasmodiophora brassicae, agente causal da hérnia das crucíferas. 2007. viii, 65 f. Tese (doutorado) - Universidade Estadual Paulista, Faculdade de Ciências Agronômicas de Botucatu, 2007.