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草酸代谢有助于杨树叶枯病菌的完全毒力和分生孢子盘发育。

Oxalic Acid Metabolism Contributes to Full Virulence and Pycnidial Development in the Poplar Canker Fungus .

机构信息

Beijing Key Laboratory for Forest Pest Control, College of Forestry, Beijing Forestry University, Beijing, China.

出版信息

Phytopathology. 2020 Jul;110(7):1319-1325. doi: 10.1094/PHYTO-10-19-0381-R. Epub 2020 Apr 30.

Abstract

Poplar Cytospora canker, which is mainly caused by , is one of the most destructive and widespread tree diseases worldwide. Although oxalic acid (OA) is demonstrated as an important virulence determinant in several necrotrophic fungi, specific functions of OA during pathogenesis remain controversial. Here, we identified three genes (, and ) directly involved in OA biosynthesis and catabolism in . We demonstrated that is required for OA biogenesis. All three genes were found to be highly upregulated during early infection stages of the poplar stem. The deletion of any of the three genes led to an obvious reduction of pycnidial production but no abnormality of hyphal growth and morphology. Furthermore, the individual deletion strain exhibited significantly limited lesion sizes on poplar twigs and leaves. Exogenous application of OA or citric acid can complement the virulence defects of Δ and Δ strains. We further found that the Δ strain strongly promoted reactive oxygen species burst of poplar leaves during infection. Finally, induced secretion of OA was observed by monitoring color change of the plates after poplar stem extracts were added in the cultures; however, we failed to quantify OA concentration by high-performance liquid chromatography. Taken together, the present results provide insights into the function of OA acting as an important virulence factor of .

摘要

杨树叶枯病主要由 引起,是全球破坏性最大和分布最广的树木疾病之一。尽管草酸(OA)已被证明是几种坏死型真菌中的一个重要毒力决定因素,但 OA 在发病机制中的具体功能仍存在争议。在此,我们在 中鉴定出了三个直接参与 OA 生物合成和分解代谢的基因(、和 )。我们证明 对于 OA 的生物合成是必需的。在杨树茎早期感染阶段,这三个基因均被高度上调。三个基因中的任何一个缺失都会导致产分生孢子结构明显减少,但不会影响菌丝生长和形态。此外,单个缺失菌株在杨树嫩枝和叶片上的病斑大小明显减小。外源性添加 OA 或柠檬酸可以弥补 Δ 和 Δ 菌株的毒力缺陷。我们进一步发现,Δ 菌株在感染过程中强烈促进了杨树叶片中活性氧的爆发。最后,通过在培养物中添加杨树茎提取物后监测平板颜色变化来观察到 OA 的诱导分泌;然而,我们未能通过高效液相色谱法定量 OA 浓度。总之,这些结果为 OA 作为 的一个重要毒力因子的作用提供了深入了解。

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