Unveiling the resistance risk and resistance mechanism of florylpicoxamid in Corynespora cassiicola from cucumber

被引:1
|
作者
Peng, Qin [1 ]
Hao, Xinchang [2 ]
Liu, Chunyue [2 ]
Li, Xiuhuan [2 ]
Lu, Xingxing [2 ]
Liu, Xili [2 ,3 ]
机构
[1] Northwest A&F Univ, Coll Plant Protect,Minist Agr & Rural Affairs, Key Lab Plant Protect Resources & Pest Management, Minist Educ,Key Lab Integrated Pest Management Cro, Yangling, Peoples R China
[2] Northwest A&F Univ, Coll Plant Protect, State Key Lab Crop Stress Resistance & High Effici, Yangling 712100, Shaanxi, Peoples R China
[3] China Agr Univ, Coll Plant Protect, Dept Plant Pathol, 2 Yuanmingyuanxi Rd, Beijing 100193, Peoples R China
关键词
Corynespora cassiicola; Florylpicoxamid; Fungicide resistance; Point mutation; Allele-specific PCR; SENSITIVITY; FUNGICIDES;
D O I
10.1016/j.pestbp.2024.106228
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Florylpicoxamid, a QiI fungicide, demonstrates broad-spectrum activity against a wide range of phytopathogenic organisms belonging to the phyla Basidiomycota and Ascomycota. Nevertheless, the potential for resistance and the underlying resistance mechanisms of Corynespora cassiicola against florylpicoxamid are still not fully understood. We determined the baseline sensitivity levels of 101 C. cassiicola isolates to florylpicoxamid. The EC50 values varied from 0.01 to 1.18 mu g/mL with an average of 0.50 mu g/mL. Laboratory-induced fungicide adaptation of nine wild-type isolates generated seven C. cassiicola mutants exhibiting high level of resistance to florylpicoxamid, all originating from a single parental isolate. The mutants maintained their resistance even after undergoing ten successive cultivations on a medium devoid of fungicides. No cross-resistance was detected between florylpicoxamid and pyraclostrobin, fluopyram, prochloraz, or propineb. Five of the resistant mutants showed an improved compound fitness index (CFI) relative to their parental isolate, whereas the remainder displayed either a reduced or comparable CFI. All seven of the resistant mutants displayed an A37V substitution within the CcCytb protein, which was responsible for the resistance to florylpicoxamid, as validated through molecular docking analysis. Furthermore, an allele-specific PCR (AS-PCR) method for detecting the CcCytbA37V mutation was successfully established. In summarize, the findings of this study indicate a moderate risk of C. cassiicola developing resistance to florylpicoxamid, with the A37V substitution in CcCytb playing a key role in this resistance, detectable through the use of specific AS-PCR primers.
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页数:8
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