Department of Botany, Faculty of Agriculture and Biology, Warsaw University of Life Sciences-SGGW, Nowoursynowska Street 159, 02-776 Warsaw, Poland.
Department of Biological Sciences, Northern Illinois University, DeKalb, IL 60115, USA.
Int J Mol Sci. 2018 Aug 4;19(8):2287. doi: 10.3390/ijms19082287.
One type of monitoring system in a plant cell is the cell wall, which intensively changes its structure during interaction with pathogen-stress factors. The wall plays a role as a dynamic and controlled structure, although it is not fully understood how relevant these modifications are to the molecular mechanisms during plant⁻virus interactions. In this work we localise the non-cellulosic polysaccharides such as xyloglucan, xylan (xylan-1) and xyloglucosyl transferase (XTH-Xet5), the enzyme that participates in the metabolism of xyloglucan. This provided us with information about the in situ distribution of the components of the hemicellulotic cell wall matrix in hypersensitive and susceptible potato⁻PVY interactions. The loosening of the cell wall was accompanied by an increase in xylan depositions during susceptible interactions, whereas, during the hypersensitive response, when the cell wall was reinforced, the xylan content decreased. Moreover, the PVY inoculation significantly redirected XTH-Xet5 depositions, regardless of types of interactions, compared to mock-inoculated tissues. Furthermore, the immunogold localisation clearly revealed the domination of Xet5 in the cell wall and in vesicles in the susceptible host. In contrast, in the resistant host increased levels of Xet5 were observed in cytoplasm, in the cell wall and in the trans-Golgi network. These findings show that the hypersensitive reaction activated XTH-Xet5 in the areas of xyloglucan endo-transglycosylase (XET) synthesis, which was then actively transported to cytoplasm, cell wall and to vacuoles. Our results provide novel insight into cell wall reorganisation during PVY infection as a response to biotic stress factors. These novel findings help us to understand the mechanisms of defence responses that are incorporated into the cell wall signalling network.
植物细胞中的一种监测系统是细胞壁,它在与病原体应激因子相互作用时会强烈改变其结构。细胞壁起着动态和可控结构的作用,尽管人们尚不完全了解这些修饰与植物-病毒相互作用过程中的分子机制有何相关。在这项工作中,我们定位了非纤维素多糖,如木葡聚糖、木聚糖(木聚糖-1)和木葡聚糖转移酶(XTH-Xet5),该酶参与木葡聚糖的代谢。这为我们提供了有关在马铃薯-PVY 相互作用中敏感和易感过程中半纤维素细胞壁基质成分的原位分布信息。细胞壁的松弛伴随着易感相互作用中木聚糖沉积的增加,而在细胞壁增强的超敏反应中,木聚糖含量减少。此外,与模拟接种组织相比,PVY 接种显著改变了 XTH-Xet5 的沉积,无论相互作用类型如何。此外,免疫胶体金定位清楚地显示了 Xet5 在易感宿主细胞壁和小泡中的主导地位。相比之下,在抗性宿主中,细胞质、细胞壁和反式高尔基体网络中观察到 Xet5 水平增加。这些发现表明,超敏反应在木葡聚糖内切糖基转移酶(XET)合成的区域激活了 XTH-Xet5,然后将其主动运输到细胞质、细胞壁和液泡中。我们的研究结果为 PVY 感染期间细胞壁重组作为生物应激因子的反应提供了新的见解。这些新发现有助于我们理解整合到细胞壁信号网络中的防御反应机制。