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转录组分析揭示中国梨品种抗梨火疫病新机制

Transcriptomics Analysis of the Chinese Pear Pathotype of Gives Insights into Novel Mechanisms of HSAF Antifungal Activities.

机构信息

Institute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Jiangsu Key Laboratory for Food Quality and Safety-State Key Laboratory Cultivation Base of Ministry of Science and Technology, Nanjing 210014, China.

College of Plant Protection, Anhui Agricultural University, Hefei 230036, China.

出版信息

Int J Mol Sci. 2018 Jun 22;19(7):1841. doi: 10.3390/ijms19071841.

Abstract

(Fries) Keissler is a lethal pear pathogen that causes leaf black spot disease of pear in Southern China. Heat-stable activity factor (HSAF) is a polycyclic tetramate macrolactam (PTM) produced by and many other microbes with a broad-spectrum antifungal activity against many filamentous fungi. In this study, we evaluated the antifungal effect of HSAF against and proposed its antifungal mechanism in . We report that HSAF inhibited the mycelial growth of in a dose-dependent manner. Transcriptomics analysis revealed that HSAF treatment resulted in an expression alteration of a wide range of genes, with 3729 genes being up-regulated, and 3640 genes being down-regulated. Furthermore, we observed that HSAF treatment disrupted multiple signaling networks and essential cellular metabolisms in , including the AMPK signaling pathway, sphingolipid metabolism and signaling pathway, carbon metabolism and the TCA (tricarboxylic acid) cycle, cell cycle, nitrogen metabolism, cell wall synthesis and a key hub protein phosphatase 2A (PP2A). These observations suggest that HSAF breaches metabolism networks and ultimately induces increased thickness of the cell wall and apoptosis in The improved understanding of the antifungal mechanism of HSAF against filamentous fungi will aid in the future identification of the direct interaction target of HSAF and development of HSAF as a novel bio-fungicide.

摘要

(弗里斯)基斯勒是一种致命的梨病原菌,可导致中国南方的梨叶黑斑病。热稳定活性因子(HSAF)是一种多环四肽大环内酯(PTM),由 和许多其他微生物产生,对许多丝状真菌具有广谱抗真菌活性。在这项研究中,我们评估了 HSAF 对 的抗真菌作用,并提出了其在 中的抗真菌机制。我们报告 HSAF 以剂量依赖的方式抑制 的菌丝生长。转录组学分析显示,HSAF 处理导致广泛基因的表达改变,其中 3729 个基因上调,3640 个基因下调。此外,我们观察到 HSAF 处理破坏了 的多个信号网络和重要的细胞代谢,包括 AMPK 信号通路、鞘脂代谢和信号通路、碳代谢和 TCA(三羧酸)循环、细胞周期、氮代谢、细胞壁合成和关键枢纽蛋白磷酸酶 2A(PP2A)。这些观察结果表明,HSAF 破坏了代谢网络,最终导致 的细胞壁增厚和细胞凋亡。深入了解 HSAF 对丝状真菌的抗真菌机制将有助于未来确定 HSAF 的直接作用靶标,并将 HSAF 开发为新型生物杀菌剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f261/6073358/793418cc62d7/ijms-19-01841-g001.jpg

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