Hao Xinchang, Li Yiwen, Hang Zhaoyue, Chen Yue, Tang Yidong, Miao Jianqiang, Peng Qin, Liu Xili
State Key Laboratory for Crop Stress Resistance and High-Efficiency Production, College of Plant Protection, Northwest A&F University, Yangling, 712100, Shaanxi, China.
Key Laboratory of Plant Protection Resources and Pest Management of Ministry of Education, Key Laboratory of Integrated Pest Management On Crops in Northwestern Loess Plateau of Ministry of Agriculture and Rural Affairs, College of Plant Protection, Northwest A&F University, Yangling, 712100, Shaanxi, China.
Stress Biol. 2025 Sep 1;5(1):53. doi: 10.1007/s44154-025-00251-8.
Cucumber target spot, a major disease that threatens cucumber production, is caused by Corynespora cassiicola. Cyclobutrifluram, a novel succinate dehydrogenase inhibitor (SDHI) developed by Syngenta, has demonstrated strong inhibitory activity against various plant pathogenic fungi and nematodes. However, its antifungal spectrum, resistance risk as well as underlying mechanisms of resistance in C. cassiicola remain poorly understood. In this study, cyclobutrifluram exhibited potent inhibitory activity against anamorphic fungi and selected ascomycetes, with the mean sensitivity of C. cassiicola isolates to the fungicide being 0.98 ± 1.26 μg/mL. Additionally, five laboratory-derived cyclobutrifluram-resistant mutants showed comparable or lower biological fitness than their respective parental isolates. The resistant mutants and field isolates were also found to possess nine distinct point mutations in the CcSdhB, CcSdhC or CcSdhD genes. Finally, cyclobutrifluram exhibited positive cross-resistance with other SDHIs, with the resistance levels varying depending on the specific mutations present. In conclusion, cyclobutrifluram was found to be effective against anamorphic fungi and selected ascomycetes. C. cassiicola's risk of resistance development to cyclobutrifluram was assessed as moderate to high and was primarily associated with mutations in CcSdh genes.
黄瓜靶斑病是一种威胁黄瓜生产的主要病害,由多主棒孢引起。环氟菌胺是先正达公司研发的一种新型琥珀酸脱氢酶抑制剂(SDHI),已证明对多种植物病原真菌和线虫具有强大的抑制活性。然而,其抗真菌谱、抗药性风险以及多主棒孢的抗药潜在机制仍知之甚少。在本研究中,环氟菌胺对无性型真菌和选定的子囊菌表现出强大的抑制活性,多主棒孢分离株对该杀菌剂的平均敏感性为0.98±1.26μg/mL。此外,五个实验室诱导的环氟菌胺抗性突变体与其各自的亲本分离株相比,表现出相当或更低的生物学适应性。抗性突变体和田间分离株在CcSdhB、CcSdhC或CcSdhD基因中也被发现具有九个不同的点突变。最后,环氟菌胺与其他SDHIs表现出正交互抗性,抗性水平因存在的特定突变而异。总之,发现环氟菌胺对无性型真菌和选定的子囊菌有效。多主棒孢对环氟菌胺产生抗性的风险被评估为中到高,且主要与CcSdh基因的突变有关。