Haibing Ouyang, Guangzheng Sun, Kainan Li, Rui Wang, Xiaoyu Lv, Zhichao Zhang, Rong Zhao, Ying Wang, Haidong Shu, Haibin Jiang, Sicong Zhang, Jinbin Wu, Qi Zhang, Xi Chen, Tengfei Liu, Wenwu Ye, Yan Wang, Yuanchao Wang
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This revealed P. pachyrhizi infection leads to significant changes in gene expression with 10 co-expressed gene modules, representing dramatic transcriptional shifts in metabolism and signal transduction during different stages throughout the infection cycle. Numerous genes encoding secreted protein are biphasic expressed, and are capable of inhibiting programmed cell death triggered by microbial effectors. Notably, three co-expressed P. pachyrhizi apoplastic effectors (PpAE1, PpAE2, and PpAE3) were found to suppress plant immune responses and were essential for P. pachyrhizi infection. Double-stranded RNA coupled with nanomaterials significantly inhibited SBR infection by targeting PpAE1, PpAE2, and PpAE3, and provided long-lasting protection to soybean against P. pachyrhizi. Together, this study revealed prominent changes in gene expression associated with SBR and identified P. pachyrhizi virulence effectors as promising targets of RNA interference-based soybean protection strategy against SBR.</p>","PeriodicalId":195,"journal":{"name":"Journal of Integrative Plant Biology","volume":null,"pages":null},"PeriodicalIF":9.3000,"publicationDate":"2024-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Profiling of Phakopsora pachyrhizi transcriptome revealed co-expressed virulence effectors as prospective RNA interference targets for soybean rust management.\",\"authors\":\"Haibing Ouyang, Guangzheng Sun, Kainan Li, Rui Wang, Xiaoyu Lv, Zhichao Zhang, Rong Zhao, Ying Wang, Haidong Shu, Haibin Jiang, Sicong Zhang, Jinbin Wu, Qi Zhang, Xi Chen, Tengfei Liu, Wenwu Ye, Yan Wang, Yuanchao Wang\",\"doi\":\"10.1111/jipb.13772\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Soybean rust (SBR), caused by an obligate biotrophic pathogen Phakopsora pachyrhizi, is a devastating disease of soybean worldwide. 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引用次数: 0
摘要
大豆锈病(SBR)是由一种必须生物营养型病原体大豆锈菌(Phakopsora pachyrhizi)引起的,是全球大豆的一种毁灭性病害。然而,人们对 P. pachyrhizi 侵染植物的机制知之甚少,这阻碍了 SBR 有效控制策略的开发。在此,我们对 P. pachyrhizi 在大豆中的感染周期进行了详细的组织学表征,并对 P. pachyrhizi 在感染过程中的转录进行了高分辨率剖析。结果显示,P. pachyrhizi 感染导致了基因表达的显著变化,有 10 个共表达基因模块,代表了整个感染周期不同阶段代谢和信号转导过程中转录的巨大变化。许多编码分泌蛋白的基因呈双相表达,能够抑制微生物效应物引发的细胞程序性死亡。值得注意的是,三种共同表达的 P. pachyrhizi 细胞外效应因子(PpAE1、PpAE2 和 PpAE3)被发现抑制植物免疫反应,并且对 P. pachyrhizi 感染至关重要。双链 RNA 与纳米材料的结合通过靶向 PpAE1、PpAE2 和 PpAE3 显著抑制了 SBR 的感染,并为大豆提供了针对 Pachyrhizi 的持久保护。总之,本研究揭示了与 SBR 相关的基因表达的显著变化,并确定了 P. pachyrhizi 毒力效应因子是基于 RNA 干扰的大豆抗 SBR 保护策略的前景目标。
Profiling of Phakopsora pachyrhizi transcriptome revealed co-expressed virulence effectors as prospective RNA interference targets for soybean rust management.
Soybean rust (SBR), caused by an obligate biotrophic pathogen Phakopsora pachyrhizi, is a devastating disease of soybean worldwide. However, the mechanisms underlying plant invasion by P. pachyrhizi are poorly understood, which hinders the development of effective control strategies for SBR. Here we performed detailed histological characterization on the infection cycle of P. pachyrhizi in soybean and conducted a high-resolution transcriptional dissection of P. pachyrhizi during infection. This revealed P. pachyrhizi infection leads to significant changes in gene expression with 10 co-expressed gene modules, representing dramatic transcriptional shifts in metabolism and signal transduction during different stages throughout the infection cycle. Numerous genes encoding secreted protein are biphasic expressed, and are capable of inhibiting programmed cell death triggered by microbial effectors. Notably, three co-expressed P. pachyrhizi apoplastic effectors (PpAE1, PpAE2, and PpAE3) were found to suppress plant immune responses and were essential for P. pachyrhizi infection. Double-stranded RNA coupled with nanomaterials significantly inhibited SBR infection by targeting PpAE1, PpAE2, and PpAE3, and provided long-lasting protection to soybean against P. pachyrhizi. Together, this study revealed prominent changes in gene expression associated with SBR and identified P. pachyrhizi virulence effectors as promising targets of RNA interference-based soybean protection strategy against SBR.
期刊介绍:
Journal of Integrative Plant Biology is a leading academic journal reporting on the latest discoveries in plant biology.Enjoy the latest news and developments in the field, understand new and improved methods and research tools, and explore basic biological questions through reproducible experimental design, using genetic, biochemical, cell and molecular biological methods, and statistical analyses.