Guerrero Felix D, Pruett John H, Li Andrew Y
USDA-ARS, Knipling-Bushland US Livestock Insects Research Laboratory, 2700 Fredericksburg Rd., Kerrville, TX 78028, USA.
Exp Appl Acarol. 2002;28(1-4):257-64. doi: 10.1023/a:1025319104529.
We examined pyrethroid resistant Mexican strains of Boophilus microplus using biochemical and molecular tests to determine the mechanisms conferring resistance. Permethrin hydrolysis assays and esterase activity gels indicated enhanced esterase-mediated metabolic detoxification in the Cz strain, while one other pyrethroid resistant strain, SF, and two pyrethroid susceptible strains had lower levels of permethrin hydrolysis. Results from assays using a PCR-based test to detect a pyrethroid target site resistance-associated mutation in the tick sodium channel gene found only low levels of mutations in the Cz strain, while the SF strain had a high level of the mutated sodium channel alleles. A specific esterase, designated CzEst9, believed to be responsible for the esterase-mediated pyrethroid resistance in the Cz strain was purified, and the gene encoding CzEst9 cloned.
我们使用生化和分子检测方法对墨西哥的抗拟除虫菊酯微小牛蜱菌株进行了研究,以确定其抗药机制。氯菊酯水解试验和酯酶活性凝胶显示,Cz菌株中酯酶介导的代谢解毒作用增强,而另一个抗拟除虫菊酯菌株SF以及两个拟除虫菊酯敏感菌株的氯菊酯水解水平较低。使用基于PCR的检测方法来检测蜱虫钠通道基因中与拟除虫菊酯靶位点抗性相关的突变,结果发现Cz菌株中的突变水平较低,而SF菌株中突变的钠通道等位基因水平较高。一种名为CzEst9的特定酯酶被认为是Cz菌株中酯酶介导的拟除虫菊酯抗性的原因,该酯酶被纯化,并克隆了编码CzEst9的基因。