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FoMyo5 肌动蛋白结构域取代(缬氨酸突变为丙氨酸和丝氨酸突变为苏氨酸)导致尖孢镰刀菌对杀菌剂苯霜灵产生天然抗性。

FoMyo5 motor domain substitutions (Val to Ala and Ser to Thr) cause natural resistance to fungicide phenamacril in Fusarium oxysporum.

机构信息

College of Plant Protection, Nanjing Agricultural University, Key Laboratory of Pesticide, Nanjing 210095, Jiangsu Province, China; School of Life Science and Food Engineering, Huaiyin Institute of Technology, Huaian 223003, Jiangsu Province, China.

Department of Biochemistry and Molecular Biology, University of Massachusetts, Amherst 01003, MA, United States.

出版信息

Pestic Biochem Physiol. 2018 May;147:119-126. doi: 10.1016/j.pestbp.2017.12.007. Epub 2017 Dec 28.

DOI:10.1016/j.pestbp.2017.12.007
PMID:29933981
Abstract

Fusarium oxysporum (Fo) is an important genus of filamentous fungi that causes many devastating diseases of agronomical plants and some opportunistic diseases of humans. Previous studies have indicated that mutations in myosin5 acquired resistance to phenamacril in Fusarium graminearum (Fg). Here, we need to determine the residues of FoMyo5 involved in the natural resistance of plant pathogenic Fo strains. Six kinds of Fo reference strains from different hosts were studied. Fungicide susceptibility testing showed that these Fo strains demonstrated different resistance or susceptibility to phenamacril, which is Fusarium-specific antifungal compound, compared with Fg species. When aligned these homologous myosin5 motor domains of these strains, we found that the substitutions (Val to Ala and Ser to Thr) in FoMyo5 cause natural resistance to phenamacril in the plant pathogenic Fo strains. And we confirmed this result by gene replacement strategy. Such a phenomenon impeded the practical development of this fungicide for controlling vascular wilt diseases.

摘要

尖孢镰刀菌(Fusarium oxysporum,Fo)是一种重要的丝状真菌属,可引起许多农业植物的毁灭性疾病和一些人类机会性疾病。先前的研究表明,肌球蛋白 5 的突变可导致禾谷镰刀菌(Fusarium graminearum,Fg)对苯甲酰胺的耐药性。在这里,我们需要确定 FoMyo5 中参与植物病原 Fo 菌株天然抗性的残基。研究了来自不同宿主的六种 Fo 参考菌株。杀菌剂敏感性测试表明,与 Fg 种相比,这些 Fo 菌株对苯甲酰胺表现出不同的耐药性或敏感性,苯甲酰胺是一种特定于镰刀菌的抗真菌化合物。当对这些菌株的同源肌球蛋白 5 马达结构域进行比对时,我们发现 FoMyo5 中的取代(缬氨酸到丙氨酸和丝氨酸到苏氨酸)导致植物病原 Fo 菌株对苯甲酰胺产生天然抗性。我们通过基因替换策略证实了这一结果。这种现象阻碍了该杀菌剂在控制维管束萎蔫病方面的实际发展。

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引用本文的文献

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Effects of Mutations in the Phenamacril-Binding Site of Myosin-1 on Its Motor Function and Phenamacril Sensitivity.肌球蛋白-1苯螨特结合位点突变对其运动功能和苯螨特敏感性的影响。
ACS Omega. 2020 Aug 20;5(34):21815-21823. doi: 10.1021/acsomega.0c02886. eCollection 2020 Sep 1.
2
Predicting Virulence of f. sp. Based on the Production of Mycotoxin Using a Linear Regression Model.基于线性回归模型的产毒能力预测 f. sp. 的毒力。
Toxins (Basel). 2020 Apr 14;12(4):254. doi: 10.3390/toxins12040254.
3
Structural basis of Fusarium myosin I inhibition by phenamacril.
真菌肌球蛋白 I 被苯甲酰胺抑制的结构基础。
PLoS Pathog. 2020 Mar 12;16(3):e1008323. doi: 10.1371/journal.ppat.1008323. eCollection 2020 Mar.
4
Phenamacril is a reversible and noncompetitive inhibitor of class I myosin.苯马奎尔是 I 类肌球蛋白的可逆非竞争性抑制剂。
J Biol Chem. 2019 Jan 25;294(4):1328-1337. doi: 10.1074/jbc.RA118.005408. Epub 2018 Nov 30.