NADPH氧化酶在杨树溃疡病真菌黄胚胞孢子的氧化还原稳态调控及发病机制中的作用。

Quansheng Li, Rongrong Guo, Aining Li, Yonglin Wang
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引用次数: 0

摘要

杨树溃疡病是由真菌黄孢菌(Cytospora chrysosperma)引起的,在中国杨树人工林中造成了巨大的损失。虽然NADPH氧化酶(NOXs)在几种致病真菌的发育和致病性中起重要作用,但其在黄胚孢杆菌中的作用尚不清楚。在这项研究中,我们鉴定了三种氮氧化物基因(CcNox1, CcNox2和CcNoxR)。这3个基因在杨树枝条侵染过程中均高度上调,其中任何一个基因的缺失都严重降低了杨树枝条的毒力。此外,CcNox1或CcNoxR的缺失导致菌丝内源性活性氧产生显著增加,Ca2+内流增强,氧化还原稳态破坏和线粒体完整性受损。此外,已知毒力因子草酸的生物合成和分泌明显缺陷,外源草酸补充挽救了突变体的毒力。综上所述,我们的研究结果表明,NOXs在黄胚孢的氧化还原稳态、线粒体完整性和致病性中起着重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Roles of NADPH oxidases in regulating redox homeostasis and pathogenesis of the poplar canker fungus Cytospora chrysosperma.

Poplar canker, caused by the fungus Cytospora chrysosperma, results in tremendous losses in poplar plantations in China. Although NADPH oxidases (NOXs) play important roles in the development and pathogenicity of several pathogenic fungi, their roles in C. chrysosperma remain unclear. In this study, we characterized three NOX genes (CcNox1, CcNox2, and CcNoxR) in C. chrysosperma. All three genes were highly upregulated during poplar branch infection, and deletion of any of them severely reduced virulence on poplar branches. Furthermore, deletion of either CcNox1 or CcNoxR resulted in a significant increase in endogenous reactive oxygen species production in hyphae, enhanced influx of Ca2+, the disruption of redox homeostasis and compromised mitochondrial integrity. Moreover, biosynthesis and secretion of a known virulence factor oxalic acid was obviously defective and exogenous oxalic acid supplementation rescued the virulence of the mutants. Taken together, our findings reveal that NOXs play important roles in redox homeostasis, mitochondrial integrity and pathogenicity in C. chrysosperma.

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