Pseudomonas chlororaphis Metabolites Reduce MfCYP51 Expression and Yield Synergistic Efficacy in Mixture with Reduced Rates of Propiconazole Against DMI-Resistant Monilinia fructicola Isolates.

IF 4.4 2区 农林科学 Q1 PLANT SCIENCES Plant disease Pub Date : 2024-10-16 DOI:10.1094/PDIS-04-24-0869-RE
Johanna Wesche, Zhezheng Zeng, Chao-Xi Luo, Guido Schnabel
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Abstract

Brown rot caused by Monilinia fructicola is one of the most important diseases affecting peach production in the southeastern United States. Management often involves the use of demethylation inhibitor (DMI) fungicides, but efficacy can be compromised because of overexpression of the MfCYP51 gene encoding the 14α-demethylase of the ergosterol biosynthesis pathway. This study aimed to investigate the influence of the biorational fungicide Howler EVO containing Pseudomonas chlororaphis ASF009 metabolites on the expression of MfCYP51 in M. fructicola and associated synergy with a DMI fungicide for control of DMI-resistant strains. Mycelia from two DMI-sensitive and three DMI-resistant M. fructicola isolates were exposed or not to propiconazole (0.3 μg/ml), Howler (88.1 μg/ml), or the combination propiconazole + Howler for 6 h prior to RNA extraction. Real-time PCR indicated that Howler reduced the constitutive expression of MfCYP51 in DMI-sensitive and two of three DMI-resistant isolates. Propiconazole-induced expression of the DMI target gene was significantly reduced by Howler and by the mixture of Howler plus propiconazole in all isolates. Detached fruit studies on apple revealed that the combination of Howler plus a reduced label rate of Mentor (50 μg/ml propiconazole) was synergistic against brown rot caused by a DMI-resistant isolate in high and low inoculum spore concentration experiments (synergy values of 40.1 and 4.9, respectively). We hypothesize that the synergistic effects against M. fructicola resistant to DMI fungicides based on MfCYP51 gene overexpression can be attributed to reduced 14α demethylase production due to transcription inhibition, which may necessitate fewer DMI fungicide molecules to arrest fungal growth. The use of Howler/DMI mixtures for brown rot control warrants further investigation because such mixtures could potentially allow for reduced DMI fungicide use rates in the field without compromising yield or increased resistance selection.

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氯唑假单胞菌代谢物可减少 MfCYP51 的表达,与丙环唑混合使用可产生协同效应,降低丙环唑对耐 DMI 的果蝇科莫尼林菌分离物的药效。
由果核菌(Monilinia fructicola)引起的褐腐病是影响美国东南部桃子生产的最重要病害之一。防治方法通常包括使用去甲基化抑制剂(DMI)杀菌剂,但由于编码麦角甾醇生物合成途径 14α- 去甲基化酶的 MfCYP51 基因过度表达,药效可能会受到影响。本研究旨在探究含有绿假单胞菌 ASF009 代谢物的生物杀菌剂 Howler EVO 对果蝇中 MfCYP51 基因表达的影响,以及与 DMI 杀菌剂在控制抗 DMI 菌株方面的协同作用。在提取 RNA 之前,将两种对 DMI 敏感和三种对 DMI 抗性的果蝇菌分离菌丝暴露于或不暴露于丙环唑(0.3 µg/ml)、Howler(78.5 µg/ml)或丙环唑 + Howler 组合药剂 6 小时。实时聚合酶链式反应(Real-time PCR)表明,在对 DMI 敏感的分离株和三个对 DMI 抗性的分离株中的两个中,Howler 可减少 MfCYP51 的组成型表达。Howler 和 Howler 加丙环唑的混合物显著降低了所有分离物中丙环唑诱导的 DMI 目标基因的表达。对苹果进行的离体果实研究表明,在高、低接种孢子浓度实验中,Howler 与标签率降低的 Mentor(50 µg/ml 丙环唑)的组合对抗性 DMI 分离物引起的褐腐病具有协同作用(协同作用值分别为 40.1 和 4.9)。我们推测,基于 MfCYP51 基因的过表达对果蝇抗 DMI 杀菌剂产生的增效作用可归因于转录抑制导致的 14α 去甲基化酶生成减少,这可能需要更少的 DMI 杀菌剂分子来抑制真菌生长。使用 Howler /DMI 混合物控制褐腐病值得进一步研究,因为这种混合物有可能降低田间 DMI 杀真菌剂的使用率,而不会影响产量或增加抗性选择。
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来源期刊
Plant disease
Plant disease 农林科学-植物科学
CiteScore
5.10
自引率
13.30%
发文量
1993
审稿时长
2 months
期刊介绍: Plant Disease is the leading international journal for rapid reporting of research on new, emerging, and established plant diseases. The journal publishes papers that describe basic and applied research focusing on practical aspects of disease diagnosis, development, and management.
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