Wei Wang, Weixiong Wang, Jing Jiang, Xiangdong Bai, Kun Chen, Xiaoyue Zhang, Jingya Yang, Di Wu, Ben Niu, Guifeng Liu
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Specifically, compared to the wild-type line, the <i>PsnWRKY70</i>-overexpressing (OE) line had a higher average clustering coefficient and modularity. Furthermore, metabolomic analysis revealed that 19 differential metabolites were significantly enriched in the leaves of the OE line. Among these metabolites, coumarin compounds, such as fraxetin-8-O-glucoside (fraxin) and scopoletin-7-O-glucoside (scopolin), significantly promoted the proliferation of the genera <i>Methylobacterium</i> and <i>Achromobacter</i> with resistance to <i>A. alternata</i>. Additionally, these genera also served as connectors in the molecular ecological network of the phyllosphere microbiome of the OE line. Thus, we concluded that the <i>PsnWRKY70</i> gene enhanced the stability, complexity, and core taxa cooperation of the phyllosphere microbial network in <i>Populus</i> and regulated the biosynthesis of fraxin and scopolin to recruit beneficial bacteria controlling <i>A. alternata</i> infection. These findings provide valuable insights into the ability of resistant plant genotypes to drive the assembly of the phyllosphere microbiome, advancing our understanding of defense against pathogens using the biocontrol phyllosphere microbial community.IMPORTANCEPoplar leaf blight caused by <i>Alternaria alternata</i>, a common disease in Northeast China, can cause abnormal abscission of poplar leaves and even lead to plant death in severe cases. WRKY transcription factors have been implicated in the regulation of disease resistance associated with plant immune responses to secondary metabolism via a complicated gene network. However, little is known about how the metabolites regulated by the <i>PsnWRKY70</i> gene trigger changes in the phyllosphere microbiome, leading to increased resistance to foliar pathogens. Here, the <i>PsnWRKY70</i> overexpressing line of <i>Populus</i> (<i>Populus simonii</i> × <i>P. nigra</i>) exhibited increased coumarin synthesis in the leaves, triggering changes in microbial species central in phyllosphere microbial networks and leading to increased resistance to <i>A. alternata</i> infection. 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引用次数: 0
摘要
WRKY转录因子与植物免疫应答相关的抗病调控有关,这对植物抵御胁迫的防御反应具有重要意义。杨树PsnWRKY70基因在叶层微生物群与植物叶面病原菌防御之间的作用机制尚不清楚。分子生态网络分析表明,互交霉侵染对杨树层球细菌群落的稳定性和复杂性有影响。具体而言,与野生型相比,psnwrky70过表达(OE)系具有更高的平均聚类系数和模块化。此外,代谢组学分析显示,19种差异代谢物在OE系叶片中显著富集。在这些代谢产物中,香豆素类化合物,如黄曲霉素-8- o -葡萄糖苷(fraxin)和东莨菪碱-7- o -葡萄糖苷(scopolin),能显著促进耐药的甲基菌属和无色杆菌属的增殖。此外,这些属还在OE系层球微生物群的分子生态网络中起着连接器的作用。综上所述,PsnWRKY70基因增强了杨树层圈微生物网络的稳定性、复杂性和核心类群合作,调控了石蜡素和东scopolin的生物合成,从而招募有益菌控制杨树感染。这些发现为了解抗性植物基因型驱动叶根圈微生物群组装的能力提供了有价值的见解,促进了我们对利用生物防治叶根圈微生物群落防御病原体的理解。白杨叶枯病是东北地区的一种常见病,可引起杨树叶片异常脱落,严重者可导致植株死亡。WRKY转录因子通过复杂的基因网络参与调控与植物次生代谢免疫应答相关的抗病性。然而,关于PsnWRKY70基因调控的代谢物如何触发叶根圈微生物组的变化,从而增加对叶面病原体的抗性,人们知之甚少。结果表明,PsnWRKY70过表达的杨树(Populus simonii × P. nigra)叶片中香豆素合成增加,引发层际微生物网络中心微生物种类的变化,导致杨树对白杨侵染的抗性增强。本研究揭示了PsnWRKY70基因在杨树耐蚜机制中的作用。
Populus simonii × Populus nigra overexpressing PsnWRKY70 recruits phyllosphere bacterial strains that inhibit Alternaria alternata.
WRKY transcription factors have been implicated in the regulation of disease resistance associated with plant immune responses, which has crucial implications for defense responses against stress in plants. The role played by the PsnWRKY70 gene of Populus (Populus simonii × P. nigra) in triggering the mechanism between the phyllosphere microbiome and plant defense against foliar pathogens remains unclear. Molecular ecological network analysis demonstrated that the stability and complexity of the phyllosphere bacterial community of Populus were influenced by Alternaria alternata infection. Specifically, compared to the wild-type line, the PsnWRKY70-overexpressing (OE) line had a higher average clustering coefficient and modularity. Furthermore, metabolomic analysis revealed that 19 differential metabolites were significantly enriched in the leaves of the OE line. Among these metabolites, coumarin compounds, such as fraxetin-8-O-glucoside (fraxin) and scopoletin-7-O-glucoside (scopolin), significantly promoted the proliferation of the genera Methylobacterium and Achromobacter with resistance to A. alternata. Additionally, these genera also served as connectors in the molecular ecological network of the phyllosphere microbiome of the OE line. Thus, we concluded that the PsnWRKY70 gene enhanced the stability, complexity, and core taxa cooperation of the phyllosphere microbial network in Populus and regulated the biosynthesis of fraxin and scopolin to recruit beneficial bacteria controlling A. alternata infection. These findings provide valuable insights into the ability of resistant plant genotypes to drive the assembly of the phyllosphere microbiome, advancing our understanding of defense against pathogens using the biocontrol phyllosphere microbial community.IMPORTANCEPoplar leaf blight caused by Alternaria alternata, a common disease in Northeast China, can cause abnormal abscission of poplar leaves and even lead to plant death in severe cases. WRKY transcription factors have been implicated in the regulation of disease resistance associated with plant immune responses to secondary metabolism via a complicated gene network. However, little is known about how the metabolites regulated by the PsnWRKY70 gene trigger changes in the phyllosphere microbiome, leading to increased resistance to foliar pathogens. Here, the PsnWRKY70 overexpressing line of Populus (Populus simonii × P. nigra) exhibited increased coumarin synthesis in the leaves, triggering changes in microbial species central in phyllosphere microbial networks and leading to increased resistance to A. alternata infection. This study provides insights into the role of the PsnWRKY70 gene in triggering the resistance mechanism to A. alternata in Populus.
mSystemsBiochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍:
mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.