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首页> 外文期刊>Environmental microbiology >pH dependency of sclerotial development and pathogenicity revealed by using genetically defined oxalate-minus mutants of Sclerotinia sclerotiorum
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pH dependency of sclerotial development and pathogenicity revealed by using genetically defined oxalate-minus mutants of Sclerotinia sclerotiorum

机译:pH依赖性的硬化发育和致病性,通过使用遗传确定的草酸菌核盘菌草酸减号突变体揭示。

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The devastating plant pathogen Sclerotinia sclerotiorum produces copious (up to 50mM) amounts of oxalic acid, which, for over a quarter century, has been claimed as the pathogenicity determinant based on UV-induced mutants that concomitantly lost oxalate production and pathogenicity. Such a claim was made without fulfilling the molecular Koch's postulates because the UV mutants are genetically undefined and harbour a developmental defect in sclerotial production. Here, we generated oxalate-minus mutants of S.sclerotiorum using two independent mutagenesis techniques, and tested the resulting mutants for growth at different pHs and for pathogenicity on four host plants. The oxalate-minus mutants accumulated fumaric acid, produced functional sclerotia and have reduced ability to acidify the environment. The oxalate-minus mutants retained pathogenicity on plants, but their virulence varied depending on the pH and buffering capacity of host tissue. Acidifying the host tissue enhanced virulence of the oxalate-minus mutants, whereas supplementing with oxalate did not. These results suggest that it is low pH, not oxalic acid itself, that establishes the optimum conditions for growth, reproduction, pathogenicity and virulence expression of S.sclerotiorum. Exonerating oxalic acid as the primary pathogenicity determinant will stimulate research into identifying additional candidates as pathogenicity factors towards better understanding and managing Sclerotinia diseases.
机译:毁灭性植物病原菌核盘菌产生大量草酸(最高50mM),在四分之一世纪以来,草酸一直被认为是基于紫外线诱导的突变体的致病性决定因素,这些突变体同时会损失草酸盐的产生和致病性。之所以提出这样的主张,是因为没有满足科赫分子的假设,因为紫外线突变体在遗传上是不确定的,并且在硬化产生中具有发育缺陷。在这里,我们使用两种独立的诱变技术生成了S.sclerotiorum的草酸盐减号突变体,并测试了所得突变体在不同pH下的生长以及对四种宿主植物的致病性。草酸减负突变体会富集富马酸,产生功能性菌核并降低酸化环境的能力。草酸减号突变体保留了植物的致病性,但其毒性取决于宿主组织的pH和缓冲能力。酸化宿主组织可增强草酸减负突变体的毒性,而补充草酸则不会。这些结果表明,低pH而不是草酸本身为核盘菌的生长,繁殖,致病性和毒力表达建立了最佳条件。草酸作为主要的致病性决定因素将刺激研究,以寻找其他候选物作为致病性因素,以更好地了解和管理菌核病。

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