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Effect of the F129L Mutation in Alternaria solani on Fungicides Affecting Mitochondrial Respiration.链格孢菌中F129L突变对影响线粒体呼吸的杀菌剂的作用
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Impact of recently emerged sterol 14{alpha}-demethylase (CYP51) variants of Mycosphaerella graminicola on azole fungicide sensitivity.麦角甾醇 14α-脱甲基酶(CYP51)新型变体对层出镰刀菌唑类杀菌剂敏感性的影响。
Appl Environ Microbiol. 2011 Jun;77(11):3830-7. doi: 10.1128/AEM.00027-11. Epub 2011 Apr 8.
3
Lack of cross-resistance to a novel succinate dehydrogenase inhibitor, fluopyram, in highly boscalid-resistant isolates of Corynespora cassiicola and Podosphaera xanthii.高度抗波尔多液的姜炭疽菌和梨灰霉病菌对新型琥珀酸脱氢酶抑制剂氟吡菌酰胺无交叉抗性。
Pest Manag Sci. 2011 Apr;67(4):474-82. doi: 10.1002/ps.2092. Epub 2011 Jan 11.
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Mechanism of binding of prothioconazole to Mycosphaerella graminicola CYP51 differs from that of other azole antifungals.丙硫菌唑与禾谷丝核菌 CYP51 的结合机制不同于其他唑类抗真菌药物。
Appl Environ Microbiol. 2011 Feb;77(4):1460-5. doi: 10.1128/AEM.01332-10. Epub 2010 Dec 17.
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Multiple mechanisms account for resistance to sterol 14α-demethylation inhibitors in field isolates of Mycosphaerella graminicola.麦类球腔菌田间分离物对甾醇 14α-脱甲基抑制剂产生抗性的多种机制。
Pest Manag Sci. 2011 Jan;67(1):44-59. doi: 10.1002/ps.2028. Epub 2010 Oct 14.
6
Exploring mechanisms of resistance to respiratory inhibitors in field strains of Botrytis cinerea, the causal agent of gray mold.探索灰霉病菌(Botrytis cinerea)田间菌株对呼吸抑制剂产生抗药性的机制,该病菌是灰霉病的病原体。
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A novel substitution I381V in the sterol 14alpha-demethylase (CYP51) of Mycosphaerella graminicola is differentially selected by azole fungicides.在麦角甾醇 14α-脱甲基酶(CYP51)中发现的一个新的 I381V 取代,是由唑类杀菌剂差异选择的。
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Identification and characterisation of Mycosphaerella graminicola secreted or surface-associated proteins with variable intragenic coding repeats.鉴定和表征具可变内含子编码重复的禾谷球腔菌分泌或表面相关蛋白。
Fungal Genet Biol. 2010 Jan;47(1):19-32. doi: 10.1016/j.fgb.2009.10.009.
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Identification of three mutant loci conferring carboxin-resistance and development of a novel transformation system in Aspergillus oryzae.米曲霉中赋予萎锈灵抗性的三个突变位点的鉴定及一种新型转化系统的开发
Fungal Genet Biol. 2009 Jan;46(1):67-76. doi: 10.1016/j.fgb.2008.10.005. Epub 2008 Oct 21.
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Phytopathology. 2005 Aug;95(8):933-41. doi: 10.1094/PHYTO-95-0933.

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.

DOI:10.1111/j.1364-3703.2011.00746.x
PMID:21933337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6638775/
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。