Feng Ji, Cai Liu-Ti, Li Tao, Wang Han-Cheng, Zhang Chuan-Qing
Department of Crop Protection, Zhejiang Agriculture and Forest University, Hangzhou, China.
Guizhou Academy of Tobacco Plant Science, Guiyang, China.
Pest Manag Sci. 2025 Jun;81(6):2891-2900. doi: 10.1002/ps.8654. Epub 2025 Jan 15.
Tobacco brown spot (TBS) caused by Alternaria alternata is one of the most common diseases of tobacco in China, resulting in large loss in yield and quality. Demethylation inhibitors (DMIs) such as tebuconazole are commonly used pesticides to control TBS. However, their control effect has shown a downward trend in recent years. In this study, the occurrence and molecular mechanism of resistance to tebuconazole in Alternaria alternata were analyzed.
The resistance of 63 strains of Alternaria alternata to tebuconazole was investigated with the concentration of 5 and 20 μg/mL as the identification standard, and the resistance frequency was as high as 93.65%. It was found that the target mutation from G to S at the 462nd amino acid position of CYP51 was the cause of moderate resistance to tebuconazole in A. alternata. Molecular docking analysis further confirmed that the G462S mutation of AaCYP51 decreased the binding affinity of tebuconazole to CYP51. The artificial AaCYP51-G462S transformants based on wild-sensitive GZA-24 showed resistance to tebuconazole and cross-resistance to metconazole and prothioconazole. In the present investigation, the virulence of the CYP51-G462S mutant was reduced, while mycelial growth, sporulation, and conidial germination did not change in comparison with the progenitor strain GZA-24. In addition, the mutants containing the G462S mutation in AaCYP51 exhibited decreased sensitivity to high osmotic stress stimulated by 1 M NaCl, and the capacity to respond to cell wall- and cytomembrane-damaging agents did not change in the mutants.
The G462S substitution of CYP51 is the main factor for the moderate resistance to tebuconazole in A. alternata and mechanisms other than CYP51-target mutation might be involved in tebuconazole lowly resistant isolates. © 2025 Society of Chemical Industry.
由链格孢引起的烟草赤星病是中国烟草最常见的病害之一,导致产量和品质大幅损失。戊唑醇等脱甲基抑制剂(DMI)是防治烟草赤星病常用的农药。然而,近年来它们的防治效果呈下降趋势。本研究分析了链格孢对戊唑醇的抗性发生情况及其分子机制。
以5和20μg/mL的浓度为鉴定标准,对63株链格孢对戊唑醇的抗性进行了研究,抗性频率高达93.65%。发现CYP51第462位氨基酸位置由G突变为S是链格孢对戊唑醇产生中等抗性的原因。分子对接分析进一步证实,AaCYP51的G462S突变降低了戊唑醇与CYP51的结合亲和力。基于野生敏感菌株GZA - 24构建的人工AaCYP51 - G462S转化体对戊唑醇具有抗性,并对丙环唑和噻呋酰胺具有交叉抗性。在本研究中,CYP51 - G462S突变体的毒力降低,而与亲本菌株GZA - 24相比,其菌丝生长、产孢和分生孢子萌发没有变化。此外,AaCYP51中含有G462S突变的突变体对1 M NaCl刺激的高渗胁迫敏感性降低,并且突变体对细胞壁和细胞膜损伤剂的反应能力没有变化。
CYP51的G462S替换是链格孢对戊唑醇产生中等抗性的主要因素,除CYP51靶点突变外的其他机制可能与戊唑醇低抗分离株有关。© 2025化学工业协会。