Délye C, Laigret F, Corio-Costet M F
Unité de Recherches Intégrées sur la Vigne, Institut National de la Recherche Agronomique, Villenave d'Ornon, France.
Appl Environ Microbiol. 1997 Aug;63(8):2966-70. doi: 10.1128/aem.63.8.2966-2970.1997.
We investigated the molecular basis of resistance of the obligate biotrophic grape powdery mildew fungus Uncinula necator to sterol demethylation-inhibiting fungicides (DMIs). The sensitivity of 91 single-spore field isolates of U. necator to triadimenol was assessed by using a leaf disc assay. Resistance factors (RF) ranged from 1.8 to 26.0. The gene encoding the target of DMIs (eburicol 14 alpha-demethylase) from five sensitive and seven resistant isolates was cloned and sequenced. A single mutation, leading to the substitution of a phenylalanine residue for a tyrosine residue at position 136, was found in all isolates exhibiting an RF higher than 5. No mutation was found in sensitive or weakly resistant (RF, < 5) isolates. An allele-specific PCR assay was developed to detect the mutation. Among the 91 isolates tested, only isolates with RF higher than 5 carried the mutation. Three of the 19 resistant isolates and all sensitive and weakly resistant isolates did not possess the mutation. The mutation at codon 136 is thus clearly associated with high levels of resistance to triadimenol.
我们研究了专性活体营养型葡萄白粉病菌(葡萄钩丝壳菌)对甾醇去甲基化抑制剂类杀菌剂(DMIs)产生抗性的分子基础。通过叶盘试验评估了91个葡萄钩丝壳菌单孢田间分离株对三唑醇的敏感性。抗性因子(RF)范围为1.8至26.0。从5个敏感分离株和7个抗性分离株中克隆并测序了编码DMIs作用靶标的基因(依布瑞醇14α-去甲基酶)。在所有抗性因子高于5的分离株中均发现了一个单一突变,该突变导致第136位的酪氨酸残基被苯丙氨酸残基取代。在敏感或弱抗性(RF < 5)分离株中未发现突变。开发了一种等位基因特异性PCR检测方法来检测该突变。在测试的91个分离株中,只有抗性因子高于5的分离株携带该突变。19个抗性分离株中的3个以及所有敏感和弱抗性分离株均不具有该突变。因此,第136位密码子的突变显然与对三唑醇的高抗性水平相关。