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The LmSNF1 Gene Is Required for Pathogenicity in the Canola Blackleg Pathogen Leptosphaeria maculans

机译:LmSNF1基因是芥花油菜黑腿病病原体链球菌黄斑病的致病性所必需的。

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摘要

Leptosphaeria maculans is a fungal pathogen causing blackleg in canola. Its virulence has been attributed, among other factors, to the activity of hydrolytic cell wall degrading enzymes (CWDEs). Studies on the pathogenicity function of CWDEs in plant pathogenic fungi have been difficult due to gene redundancy. In microorganisms many CWDE genes are repressed by glucose and derepressed by the function of the sucrose non-fermenting protein kinase 1 gene (SNF1). To address the molecular function of SNF1 in L. maculans, the ortholog of SNF1 (LmSNF1) was cloned and functionally characterized using a gene knockout strategy. Growth of the LmSNF1 knockout strains was severely disrupted, as was sporulation, spore germination and the ability to attach on the plant surface. When inoculated on canola cotyledons, the LmSNF1 knockout strains could not cause any symptoms, indicating the loss of pathogenicity. The expression of 11 selected CWDE genes and a pathogenicity gene (LopB) was significantly down-regulated in the LmSNF1 knockout strains. In conclusion, knockout of LmSNF1 prevents L. maculans from properly derepressing the production of CWDEs, compromises the utilization of certain carbon sources, and impairs fungal pathogenicity on canola.
机译:Leptosphaeria maculans是一种真菌病原体,在双低油菜籽中引起黑腿病。除其他因素外,其毒性还归因于水解细胞壁降解酶(CWDE)的活性。由于基因冗余,很难研究CWDEs在植物致病真菌中的致病功能。在微生物中,许多CWDE基因被葡萄糖抑制,而蔗糖非发酵蛋白激酶1基因(SNF1)的功能抑制。为了解决SNF1在黄斑狼疮中的分子功能,使用基因敲除策略克隆了SNF1的直系同源基因(LmSNF1)并对其功能进行了表征。 LmSNF1敲除菌株的生长受到严重破坏,孢子形成,孢子萌发和附着在植物表面的能力也受到严重破坏。当将LmSNF1基因敲除菌株接种到双低油菜籽子叶上时,不会引起任何症状,表明其致病性丧失。 LmSNF1基因敲除菌株中11个选定的CWDE基因和致病性基因(LopB)的表达明显下调。总之,敲除LmSNF1可以防止黄斑狼疮恰当地抑制CWDEs的产生,损害某些碳源的利用,并损害双低油菜籽的真菌致病性。

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