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琥珀酸脱氢酶抑制剂风险评估研究,防治小麦叶枯病的新武器。

Risk assessment studies on succinate dehydrogenase inhibitors, the new weapons in the battle to control Septoria leaf blotch in wheat.

机构信息

Rothamsted Research, Plant Pathology and Microbiology Department, Harpenden, Hertfordshire AL5 2JQ, UK.

出版信息

Mol Plant Pathol. 2012 Apr;13(3):263-75. doi: 10.1111/j.1364-3703.2011.00746.x. Epub 2011 Sep 20.

Abstract

Chemical control of Septoria leaf blotch, caused by Mycosphaerella graminicola, is essential to ensure wheat yield and food security in most European countries. Mycosphaerella graminicola has developed resistance to several classes of fungicide and, with the efficacy of azoles gradually declining over time, new modes of action and/or improvements in host varietal resistance are urgently needed to ensure future sustainable disease control. Several new-generation carboxamide fungicides with broad-spectrum activity have recently been introduced into the cereal market. Carboxamides inhibit succinate dehydrogenase (Sdh) of the mitochondrial respiratory chain (complex II) but, because of their single-site specificity, these fungicides may be prone to resistance development. The objective of this study was to assess the risk of resistance development to different Sdh inhibitor (SDHI) fungicides in M. graminicola. UV mutagenesis was conducted to obtain a library of carboxin-resistant mutants. A range of SDHI resistance-conferring mutations was found in Sdh subunits B, C and D. Pathogenicity studies with a range of Sdh variants did not detect any fitness costs associated with these mutations. Most of the amino acid residues identified (e.g. B-S221P/T, B-H267F/L/N/Y, B-I269V and D-D129E/G/T) are directly involved in forming the cavity in which SDHI fungicides bind. Docking studies of SDHI fungicides in structural models of wild-type and mutated Sdh complexes also indicated which residues were important for the binding of different SDHI fungicides and showed a different binding for fluopyram. The predictive power of the model was also shown. Further diagnostic development, enabling the detection of resistant alleles at low frequencies, and cross-resistance studies will aid the implementation of anti-resistance strategies to prolong the cost-effectiveness and lifetime of SDHI fungicides.

摘要

由小麦球腔菌(Mycosphaerella graminicola)引起的叶枯病对欧洲大多数国家的小麦产量和粮食安全至关重要,因此需要用化学方法加以控制。由于小麦球腔菌对几类杀菌剂已产生抗药性,而且唑类杀菌剂的效果随着时间的推移逐渐降低,因此迫切需要新的作用模式和/或提高寄主品种的抗性,以确保未来可持续控制疾病。几种具有广谱活性的新一代羧酰胺类杀菌剂最近已被引入谷物市场。羧酰胺类杀菌剂抑制线粒体呼吸链(复合物 II)中的琥珀酸脱氢酶(Sdh),但由于其单一作用点特异性,这些杀菌剂可能容易产生抗药性。本研究旨在评估小麦球腔菌对不同琥珀酸脱氢酶抑制剂(SDHI)杀菌剂产生抗药性的风险。采用紫外线诱变获得了羧菌胺抗性突变体文库。在 Sdh 亚基 B、C 和 D 中发现了一系列赋予 SDHI 抗性的突变。用一系列 Sdh 变体进行的致病性研究未发现与这些突变相关的任何适应性成本。鉴定出的大多数氨基酸残基(例如 B-S221P/T、B-H267F/L/N/Y、B-I269V 和 D-D129E/G/T)直接参与形成 SDHI 杀菌剂结合的腔。SDHI 杀菌剂在野生型和突变型 Sdh 复合物结构模型中的对接研究还表明了哪些残基对于不同 SDHI 杀菌剂的结合很重要,并显示了氟吡菌胺的不同结合方式。该模型的预测能力也得到了展示。进一步的诊断开发,使能够以低频率检测抗性等位基因,以及交叉抗性研究,将有助于实施抗抗性策略,以延长 SDHI 杀菌剂的成本效益和使用寿命。

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