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Oxalic Acid Has an Additional Detoxifying Function in Sclerotinia sclerotiorum Pathogenesis

机译:草酸在核盘菌菌核病发病机理中具有附加的解毒功能

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摘要

The mechanism of the diseases caused by the necrotroph plant pathogen Sclerotinia sclerotiorum is not well understood. To investigate the role of oxalic acid during infection high resolution, light-, scanning-, transmission electron microscopy and various histochemical staining methods were used. Our inoculation method allowed us to follow degradation of host plant tissue around single hyphae and to observe the reaction of host cells in direct contact with single invading hyphae. After penetration the outer epidermal cell wall matrix appeared degraded around subcuticular hyphae (12-24 hpi). Calcium oxalate crystals were detected in advanced (36-48 hpi) and late (72 hpi) infection stages, but not in early stages. In early infection stages, surprisingly, no toxic effect of oxalic acid eventually secreted by S. sclerotiorum was observed. As oxalic acid is a common metabolite in plants, we propose that attacked host cells are able to metabolize oxalic acid in the early infection stage and translocate it to their vacuoles where it is stored as calcium oxalate. The effects, observed on healthy tissue upon external application of oxalic acid to non-infected, living tissue and cell wall degradation of dead host cells starting at the inner side of the walls support this idea. The results indicate that oxalic acid concentrations in the early stage of infection stay below the toxic level. In plant and fungi oxalic acid/calcium oxalate plays an important role in calcium regulation. Oxalic acid likely could quench calcium ions released during cell wall breakdown to protect growing hyphae from toxic calcium concentrations in the infection area. As calcium antimonate-precipitates were found in vesicles of young hyphae, we propose that calcium is translocated to the older parts of hyphae and detoxified by building non-toxic, stable oxalate crystals. We propose an infection model where oxalic acid plays a detoxifying role in late infection stages.
机译:由坏死性植物病原菌核盘菌引起的疾病的机理尚不清楚。为了研究草酸在感染中的作用,使用了高分辨率,光镜,扫描镜,透射电镜和各种组织化学染色方法。我们的接种方法使我们能够追踪单个菌丝周围宿主植物组织的降解,并观察与单个入侵菌丝直接接触的宿主细胞的反应。穿透后,外表皮细胞壁基质在表皮下菌丝周围(12-24 hpi)降解。草酸钙晶体在晚期(36-48 hpi)和晚期(72 hpi)感染阶段被检测到,但未在早期阶段被检测到。出人意料的是,在感染的早期阶段,没有观察到菌核菌最终分泌的草酸具有毒性作用。由于草酸是植物中常见的代谢产物,因此我们建议被攻击的宿主细胞能够在感染初期代谢草酸并将其转运至液泡中,并以草酸钙的形式储存。从草壁的内侧开始,在将草酸外部施用到未感染的活体组织上并对健康组织观察到的对健康组织的影响,以及死宿主细胞的细胞壁降解。结果表明,感染初期的草酸浓度保持在毒性水平以下。在植物和真菌中,草酸/草酸钙在钙调节中起重要作用。草酸可能会抑制细胞壁分解过程中释放的钙离子,从而保护菌丝免受感染区域中有毒钙的侵害。由于在幼年菌丝的囊泡中发现了锑酸钙沉淀,我们建议将钙转移到菌丝的较老部分,并通过构建无毒,稳定的草酸盐晶体将其排毒。我们提出了一种感染模型,其中草酸在感染后期起到解毒作用。

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