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琥珀酸脱氢酶抑制剂类杀菌剂(包括苯并烯氟菌唑)对炭疽菌属真菌的防治效果。

Efficacy of SDHI fungicides, including benzovindiflupyr, against Colletotrichum species.

作者信息

Ishii Hideo, Zhen Fan, Hu Mengjun, Li Xingpeng, Schnabel Guido

机构信息

National Institute for Agro-Environmental Sciences, Tsukuba, Ibaraki, Japan.

Clemson University, Clemson, SC, USA.

出版信息

Pest Manag Sci. 2016 Oct;72(10):1844-53. doi: 10.1002/ps.4216. Epub 2016 Feb 9.

Abstract

BACKGROUND

Colletotrichum species cause anthracnose diseases on many plants and crops. A new generation of succinate dehydrogenase inhibitors (SDHIs) was developed recently. The inhibitory activity of the five SDHI fungicides against Colletotrichum species was determined in this study.

RESULTS

Isolates of C. gloeosporioides, C. acutatum, C. cereale and C. orbiculare were insensitive (naturally resistant) to boscalid, fluxapyroxad and fluopyram on YBA agar medium. In contrast, these isolates were relatively sensitive to penthiopyrad, except for C. orbiculare. Most interestingly, benzovindiflupyr showed highest inhibitory activity against all of these four species. Benzovindiflupyr was effective against C. gloeosporioides and C. acutatum on apple and peach fruit, as well as on cucumber plants inoculated with C. orbiculare. The sdhB, sdhC and sdhD genes encoding the subunits of fungicide-targeted succinate dehydrogenase were sequenced, but, despite high polymorphisms, no apparent resistance mutations were found in Colletotrichum species.

CONCLUSIONS

This is the first report on the activity of benzovindiflupyr against Colletotrichum species. The broad-spectrum efficacy of benzovindiflupyr within the Colletotrichum genus might be exploited when designing disease management strategies against various pathogens on a wide range of crops. Other mechanism(s) than fungicide target-site modification may be responsible for differential sensitivity of Colletotrichum species to SDHI fungicides. © 2016 Society of Chemical Industry.

摘要

背景

炭疽菌属真菌可在多种植物和作物上引发炭疽病。新一代琥珀酸脱氢酶抑制剂(SDHIs)近期已研发出来。本研究测定了5种SDHI杀菌剂对炭疽菌属真菌的抑制活性。

结果

在YBA琼脂培养基上,胶孢炭疽菌、尖孢炭疽菌、禾生炭疽菌和瓜炭疽菌的分离菌株对啶酰菌胺、氟唑菌酰胺和氟吡菌酰胺不敏感(天然抗性)。相比之下,除瓜炭疽菌外,这些分离菌株对戊唑嘧菌酯相对敏感。最有意思的是,苯并烯氟菌唑对所有这4种炭疽菌表现出最高的抑制活性。苯并烯氟菌唑对苹果和桃果实上的胶孢炭疽菌和尖孢炭疽菌,以及接种瓜炭疽菌的黄瓜植株均有效。对杀菌剂作用靶标琥珀酸脱氢酶亚基的编码基因sdhB、sdhC和sdhD进行了测序,尽管存在高度多态性,但在炭疽菌属真菌中未发现明显的抗性突变。

结论

这是关于苯并烯氟菌唑对炭疽菌属真菌活性的首次报道。在设计针对多种作物上各种病原菌的病害管理策略时,可利用苯并烯氟菌唑在炭疽菌属内的广谱药效。炭疽菌属真菌对SDHI杀菌剂的不同敏感性可能是由除杀菌剂靶标位点修饰之外的其他机制造成的。© 2016化学工业协会

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