首页> 外文期刊>Crop Protection >Sensitivity of Sclerotinia sclerotiorum to fludioxonil: in vitro determination of baseline sensitivity and resistance risk.
【24h】

Sensitivity of Sclerotinia sclerotiorum to fludioxonil: in vitro determination of baseline sensitivity and resistance risk.

机译:菌核菌对氟狄克尼的敏感性:体外测定基线敏感性和耐药风险。

获取原文
获取原文并翻译 | 示例
       

摘要

This work determined the sensitivity of field populations of Sclerotinia sclerotiorum (Lib.) de Bary before exposure to the fungicide fludioxonil (=baseline sensitivity) and assessed the risk of fludioxonil resistance. The mean EC50 (Effective Concentration) and Minimum inhibitory concentration (MIC) values for fludioxonil based on inhibition of mycelial growth of 120 wild-type isolates were 0.015+or-0.005 micro g/ml and <0.05 micro g/ml, respectively. Positive cross-resistance was not detected between fludioxonil and benzimidazole fungicides but was detected between fludioxonil and dicarboximide fungicides which are considered as high resistance risk fungicides by FRAC, even though these fungicides have different molecular structures. By growing wild-type isolates on potato dextrose agar (PDA) containing sublethal concentrations of the fungicide, we obtained four fludioxonil-resistant mutants with resistance factors (EC50 resistant/EC50 sensitive phenotypes) >2000. The laboratory fludioxonil mutants were less fitter than their parental isolates in terms of mycelial radial growth, pathogenicity and sclerotial production. Moreover, on PDA amended with NaCl, the laboratory fludioxonil mutants grew more slowly than their fludioxonil-sensitive parents, especially at lower concentrations of NaCl. According to the fitness of mutants and the cross-resistance between fludioxonil and dicarboximide fungicides, phenylpyrroles can be considered to pose a moderate resistance risk. In a field trial, fludioxonil provided greater control (over 90% disease control) of S. sclerotiorum than iprodione.
机译:这项工作确定了暴露于杀菌剂氟地西尼前的巴氏核盘菌(Slerotinia sclerotiorum)(ib。)de Bary田间种群的敏感性(基线敏感性),并评估了氟地西尼耐药的风险。基于对120种野生型分离物的菌丝体生长的抑制作用,氟地西尼的EC 50 平均有效浓度和最小抑菌浓度(MIC)值为0.015+或-0.005 micro g / ml,<0.05微克/毫升。在氟地莫尼和苯并咪唑类杀真菌剂之间未检测到正交叉耐药性,但在氟地莫尼和二甲酰亚胺类杀真菌剂之间检测到正交叉耐药性,即使这些杀真菌剂具有不同的分子结构,它们也被FRAC视为具有高耐药风险的杀真菌剂。通过在含有亚致死浓度杀真菌剂的马铃薯葡萄糖琼脂(PDA)上培养野生型分离株,我们获得了具有耐药因子(EC 50 耐药/ EC 50 敏感表型)> 2000。就菌丝的径向生长,致病性和菌核产生而言,实验室氟尿酮突变体比其父母分离株更不适合。此外,在用NaCl修饰的PDA上,实验室氟硝酮突变体的生长速度比氟喹酮敏感性母体慢,尤其是在NaCl浓度较低的情况下。根据突变体的适用性和氟地西尼与二羧酰亚胺杀真菌剂之间的交叉耐药性,可以认为苯基吡咯具有中等耐药性风险。在田间试验中,氟狄索尼可更好地控制(超过90%的疾病控制)S。硬化菌素比异丙洛酮。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号