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Agrobacterium tumefaciens-mediated transformation and expression of GFP in Ascochyta lentis to characterize ascochyta blight disease progression in lentil

机译:根癌农杆菌介导的转化和GFP在小球藻中的表达以表征小扁豆枯萎病的进展

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摘要

The plant immune system is made up of a complex response network that involves several lines of defense to fight invading pathogens. Fungal plant pathogens on the other hand, have evolved a range of ways to infect their host. The interaction between Ascochyta lentis and two lentil genotypes was explored to investigate the progression of ascochyta blight (AB) in lentils. In this study, we developed an Agrobacterium tumefaciens-mediated transformation system for A. lentis by constructing a new binary vector, pATMT-GpdGFP, for the constitutive expression of green fluorescent protein (EGFP). Green fluorescence was used as a highly efficient vital marker to study the developmental changes in A. lentis during AB disease progression on the susceptible and resistant lentil accessions, ILL6002 and ILL7537, respectively. The initial infection stages were similar in both the resistant and susceptible accessions where A. lentis uses infection structures such as germ tubes and appressoria to gain entry into the host while the host uses defense mechanisms to prevent pathogen entry. Penetration was observed at the junctions between neighbouring epidermal cells and occasionally, through the stomata. The pathogen attempted to penetrate and colonize ILL7537, but further fungal advancement appeared to be halted, and A. lentis did not enter the mesophyll. Successful entry and colonization of ILL6002 coincided with structural changes in A. lentis and the onset of necrotic lesions 5–7 days post inoculation. Once inside the leaf, A. lentis continued to grow, colonizing all parts of the leaf followed by plant cell collapse. Pycnidia-bearing spores appeared 14 days post inoculation, which marks the completion of the infection cycle. The use of fluorescent proteins in plant pathogenic fungi together with confocal laser scanning microscopy, provide a valuable tool to study the intracellular dynamics, colonization strategy and infection mechanisms during plant-pathogen interaction.
机译:植物免疫系统由一个复杂的反应网络组成,该网络涉及抵御病原体的几道防线。另一方面,真菌植物病原体已经进化出多种感染宿主的方法。研究了小扁豆和两个小扁豆基因型之间的相互作用,以研究小扁豆中枯萎病(AB)的进程。在这项研究中,我们通过构建用于绿色荧光蛋白(EGFP)组成型表达的新的二元载体pATMT-GpdGFP,为根癌农杆菌开发了一种农杆菌介导的转化系统。绿色荧光被用作高效的生命标志物,分别研究易感和抗性小扁豆材料ILL6002和ILL7537在AB病进展过程中的慢链霉菌的发育变化。在抗性和易感性种质中,初始感染阶段都相似,其中扁豆曲霉利用感染结构(例如胚芽管和压感器)进入宿主,而宿主利用防御机制阻止病原体进入。在相邻表皮细胞之间的交界处观察到穿透,偶尔穿过气孔。病原体试图穿透并在ILL7537上定殖,但进一步的真菌生长似乎停止了,而扁豆曲霉也没有进入叶肉。 ILL6002的成功进入和定殖与轻度曲霉的结构变化以及接种后5-7天开始坏死性病变的发生有关。一旦进入叶片,扁豆曲霉就继续生长,在叶片的所有部分定居,随后植物细胞崩溃。在接种后14天出现了含有伪孢子虫的孢子,这标志着感染周期的完成。荧光蛋白在植物病原真菌中的应用以及共聚焦激光扫描显微镜,为研究植物与病原体相互作用过程中的细胞内动力学,定植策略和感染机制提供了有价值的工具。

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