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与靶标位点修饰及Cyp51的诱导性过表达相关的网斑病菌条形柄锈菌专化型对脱甲基酶抑制剂杀菌剂的抗性

Demethylase Inhibitor Fungicide Resistance in Pyrenophora teres f. sp. teres Associated with Target Site Modification and Inducible Overexpression of Cyp51.

作者信息

Mair Wesley J, Deng Weiwei, Mullins Jonathan G L, West Samuel, Wang Penghao, Besharat Naghmeh, Ellwood Simon R, Oliver Richard P, Lopez-Ruiz Francisco J

机构信息

Department of Environment and Agriculture, Centre for Crop and Disease Management, Curtin University Bentley, WA, Australia.

Institute of Life Science, School of Medicine, Swansea University Swansea, UK.

出版信息

Front Microbiol. 2016 Aug 19;7:1279. doi: 10.3389/fmicb.2016.01279. eCollection 2016.

Abstract

Pyrenophora teres f. sp. teres is the cause of net form of net blotch (NFNB), an economically important foliar disease in barley (Hordeum vulgare). Net and spot forms of net blotch are widely controlled using site-specific systemic fungicides. Although resistance to succinate dehydrogenase inhibitors and quinone outside inhibitors has been addressed before in net blotches, mechanisms controlling demethylation inhibitor resistance have not yet been reported at the molecular level. Here we report the isolation of strains of NFNB in Australia since 2013 resistant to a range of demethylase inhibitor fungicides. Cyp51A:KO103-A1, an allele with the mutation F489L, corresponding to the archetype F495I in Aspergillus fumigatus, was only present in resistant strains and was correlated with resistance factors to various demethylase inhibitors ranging from 1.1 for epoxiconazole to 31.7 for prochloraz. Structural in silico modeling of the sensitive and resistant CYP51A proteins docked with different demethylase inhibitor fungicides showed how the interaction of F489L within the heme cavity produced a localized constriction of the region adjacent to the docking site that is predicted to result in lower binding affinities. Resistant strains also displayed enhanced induced expression of the two Cyp51A paralogs and of Cyp51B genes. While Cyp51B was found to be constitutively expressed in the absence of fungicide, Cyp51A was only detected at extremely low levels. Under fungicide induction, expression of Cyp51B, Cyp51A2, and Cyp51A1 was shown to be 1.6-, 3,- and 5.3-fold higher, respectively in the resistant isolate compared to the wild type. These increased levels of expression were not supported by changes in the promoters of any of the three genes. The implications of these findings on demethylase inhibitor activity will require current net blotch management strategies to be reconsidered in order to avoid the development of further resistance and preserve the lifespan of fungicides in use.

摘要

网斑病菌(Pyrenophora teres f. sp. teres)是大麦(Hordeum vulgare)上经济重要性叶部病害——网斑病净斑型(NFNB)的病原菌。网斑病的净斑型和斑点型主要通过位点特异性内吸性杀菌剂进行广泛防治。尽管之前已报道过网斑病菌对琥珀酸脱氢酶抑制剂和醌外抑制剂的抗性,但在分子水平上控制脱甲基抑制剂抗性的机制尚未见报道。在此,我们报告了自2013年以来在澳大利亚分离到的对一系列脱甲基酶抑制剂杀菌剂具有抗性的NFNB菌株。Cyp51A:KO103 - A1是一个具有F489L突变的等位基因,相当于烟曲霉原型中的F495I,仅存在于抗性菌株中,并且与各种脱甲基酶抑制剂的抗性因子相关,抗环氧唑的抗性因子为1.1,抗咪鲜胺的抗性因子为31.7。对敏感和抗性CYP51A蛋白与不同脱甲基酶抑制剂杀菌剂进行对接的计算机模拟结构显示,血红素腔内F489L的相互作用如何导致对接位点附近区域的局部收缩,预计这会导致较低的结合亲和力。抗性菌株还表现出两个Cyp51A旁系同源基因和Cyp51B基因的诱导表达增强。虽然发现Cyp51B在无杀菌剂的情况下组成型表达,但Cyp51A仅在极低水平被检测到。在杀菌剂诱导下,与野生型相比,抗性分离株中Cyp51B、Cyp51A2和Cyp51A1的表达分别高出1.6倍、3倍和5.3倍。这三个基因的启动子变化并未支持这些表达水平的增加。这些发现对脱甲基酶抑制剂活性的影响将需要重新考虑当前的网斑病管理策略,以避免进一步产生抗性并延长现有杀菌剂的使用寿命。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fab/4990540/efc341382a47/fmicb-07-01279-g0001.jpg

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