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Multiple Contributions of Peroxisomal Metabolic Function to Fungal Pathogenicity in Colletotrichum lagenarium

机译:过氧化物酶体代谢功能对炭疽菌真菌致病性的多种贡献

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摘要

In Colletotrichum lagenarium, which is the causal agent of cucumber anthracnose, PEX6 is required for peroxisome biogenesis and appressorium-mediated infection. To verify the roles of peroxisome-associated metabolism in fungal pathogenicity, we isolated and functionally characterized ICL1 of C. lagenarium, which encodes isocitrate lyase involved in the glyoxylate cycle in peroxisomes. The icl1 mutants failed to utilize fatty acids and acetate for growth. Although Icl1 has no typical peroxisomal targeting signals, expression analysis of the GFP-Icl1 fusion protein indicated that Icl1 localizes in peroxisomes. These results indicate that the glyoxylate cycle that occurs inside the peroxisome is required for fatty acid and acetate metabolism for growth. Importantly, in contrast with the pex6 mutants that form nonmelanized appressoria, the icl1 mutants formed appressoria that were highly pigmented with melanin, suggesting that the glyoxylate cycle is not essential for melanin biosynthesis in appressoria. However, the icl1 mutants exhibited a severe reduction in virulence. Appressoria of the icl1 mutants failed to develop penetration hyphae in the host plant, suggesting that ICL1 is involved in host invasion. The addition of glucose partially restored virulence of the icl1 mutant. Heat shock treatment of the host plant also enabled the icl1 mutants to develop lesions, implying that the infection defect of the icl1 mutant is associated with plant defense. Together with the requirement of PEX6 for appressorial melanization, our findings suggest that peroxisomal metabolic pathways play functional roles in appressorial melanization and subsequent host invasion steps, and the latter step requires the glyoxylate cycle.
机译:在黄瓜炭疽病的病原体炭疽菌中,PEX6是过氧化物酶体生物发生和食堂介导的感染所必需的。为了验证过氧化物酶体相关代谢在真菌致病性中的作用,我们分离和功能鉴定了长毛梭菌的ICL1,其编码过氧化物酶体中乙醛酸循环中涉及的异柠檬酸裂合酶。 icl1突变体未能利用脂肪酸和乙酸盐来生长。尽管Icl1没有典型的过氧化物酶体靶向信号,但GFP-Icl1融合蛋白的表达分析表明Icl1定位在过氧化物酶体中。这些结果表明,过氧化物酶体内部发生的乙醛酸循环对于脂肪酸和乙酸酯代谢是必需的。重要的是,与形成未变黑的Appressoria的pex6突变体相反,icl1突变体形成了富含黑色素的Appressoria,这表明乙醛酸循环对于Appressoria中的黑色素生物合成不是必需的。但是,icl1突变体表现出严重的毒力降低。 icl1突变体的Appressoria无法在宿主植物中形成穿透菌丝,表明ICL1参与宿主入侵。葡萄糖的添加部分地恢复了icl1突变体的毒力。宿主植物的热休克处理还使icl1突变体能够发生损伤,这表明icl1突变体的感染缺陷与植物防御相关。连同PEX6的肠胃黑色素化要求,我们的发现表明,过氧化物酶体代谢途径在肠胃黑色素化和随后的宿主侵袭步骤中发挥功能性作用,而后者需要乙醛酸循环。

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