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Extracellular vesicles from the apoplastic fungal wheat pathogen Zymoseptoria tritici

机译:来自Applastic真菌小麦病原体Zymoseptoria tritici的细胞外囊

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The fungal pathogen Zymoseptoria tritici is a significant constraint to wheat production in temperate cropping regions around the world. Despite its agronomic impacts, the mechanisms allowing the pathogen to asymptomatically invade and grow in the apoplast of wheat leaves before causing extensive host cell death remain elusive. Given recent evidence of extracellular vesicles (EVs)—secreted, membrane-bound nanoparticles containing molecular cargo—being implicated in extracellular communication between plants and fungal pathogen, we have initiated an in vitro investigation of EVs from this apoplastic fungal wheat pathogen. We aimed to isolate EVs from Z. tritici broth cultures and examine their protein composition in relation to the soluble protein in the culture filtrate and to existing fungal EV proteomes. Zymoseptoria tritici EVs were isolated from broth culture filtrates using differential ultracentrifugation (DUC) and examined with transmission electron microscopy (TEM) and nanoparticle tracking analysis (NTA). Z. tritici EVs were observed as a heterogeneous population of particles, with most between 50 and 250?nm. These particles were found in abundance in the culture filtrates of viable Z. tritici cultures, but not heat-killed cultures incubated for an equivalent time and of comparable biomass. Bottom-up proteomic analysis using LC–MS/MS, followed by stringent filtering revealed 240 Z. tritici EV proteins. These proteins were distinct from soluble proteins identified in Z. tritici culture filtrates, but were similar to proteins identified in EVs from other fungi, based on sequence similarity analyses. Notably, a putative marker protein recently identified in Candida albicans EVs was also consistently detected in Z. tritici EVs. We have shown EVs can be isolated from the devastating fungal wheat pathogen Z. tritici and are similar to protein composition to previously characterised fungal EVs. EVs from human pathogenic fungi are implicated in virulence, but the role of EVs in the interaction of phytopathogenic fungi and their hosts is unknown. These in vitro analyses provide a basis for expanding investigations of Z. tritici EVs in planta, to examine their involvement in the infection process of this apoplastic wheat pathogen and more broadly, advance understanding of noncanonical secretion in filamentous plant pathogens.
机译:真菌病原体Zymoseptoria Tritici对全球气化种植地区的小麦产量是一个重要的限制。尽管其农艺影响,但在引起广泛的宿主细胞死亡之前仍然难以捉摸,尽管允许病原体对小麦叶子的血液侵入和生长的机制。近期近期细胞外囊(EVS)的证据 - 含有分子货物的膜结合的纳米颗粒,涉及植物和真菌病原体之间的细胞外通信,我们已经开始了来自这种吻合性真菌小麦病原体的EVS的体外研究。我们的目的是将来自Z.Tritici肉汤培养物的EV分离出来,并在培养滤液中的可溶性蛋白质和现有的真菌EV蛋白质组中检查其蛋白质组合物。使用差动超速离心(DUC)与肉汤培养滤液中分离出唑脲培养物筛网,并用透射电子显微镜(TEM)和纳米粒子跟踪分析(NTA)检查。 Z.TriticieVS被观察为异质粒子群,大多数在50到250℃之间。在活性Z.Tritici培养物的培养物滤液中发现这些颗粒在培养滤液中,但不会孵育的热杀死的培养物相当于时间和可比较的生物量。使用LC-MS / MS的自下而上的蛋白质组学分析,其次是严格滤波,显示了240 Z.Tritici EV蛋白。这些蛋白质与Z.Tritici培养物滤液中鉴定的可溶性蛋白质不同,但基于序列相似性分析,与来自其他真菌的EVS中鉴定的蛋白质不同。值得注意的是,在Z.Tritici EVS中,也一直检测到最近鉴定在Candida albicanseV的推定标记蛋白。我们已经显示了EVS可以从毁灭性真菌小麦病原体Z. tritici中分离出来并且与蛋白质组合物类似于先前特征的真菌EVS。来自人致病性真菌的EVS涉及毒力,但EVS在植物疗法真菌及其宿主的相互作用中的作用是未知的。这些体外分析为扩大植物毒素中的z. triticievs的调查提供了依据,以检查其参与这种诱导小麦病原体的感染过程,更广泛地推进丝状植物病原体中非甘露吞噬分泌。

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