利用RAPD-PCR标记对不同杀虫剂作用下棉蚜果胶蚧田间种群的研究

Hanan Salah El-Din Taha
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引用次数: 0

摘要

在埃及田间种植的棉花季节性地遭受棉铃虫Pectinophora gossypiella (Saunders)(鳞翅目:绵虱科)对果实和芽的侵害。杀虫剂的应用报告了大多数推荐的常规类别的控制失败。监测亚致死暴露后害虫DNA的变化成为研究害虫的新技术。利用4条随机扩增多态性脱氧核糖核酸分析(RAPD-PCR)引物按条带可重复性划分,采用分子标记聚合酶链反应(PCR)检测筛选4种杀虫剂处理。spinoteram、novaluron、metaflumezone和dimeuron的LC50分别为0.55、61.1、69.3和0.23。凝胶处理条带检测到47个位点,多态性范围为87% ~ 63%。同一处理样品的引物效率值PIC分别为0.361、0.34、0.34、0.355、0.262,RP为5.30,H分别为0.473、0.434、0.434、0.462、0.31,MI分别为0.10、0.1386、0.138、0.167、0.0582。采用UPMGA方法,根据Nei′s和遗传不相似度量化距离和相似度,构建系统发育树,将整个基因型分为2大聚类和6个亚聚类。RAPD引物显示等位基因数量(Na = 0.324、0.318、0.318、0.326、0.328)和有效等位基因数量(Ne = 0.571、0.569、0.558、0.574、0.5784)。固定指数(Fst)分析表明,4个处理样品的遗传多样性较高,Fst分别为0.626、0.684、0.684、0.2和0.695。4个基因型的基因流水平分别为(Nm = 0.239、0.230、0.230、0.233和0.2187)。结果表明,RAPD-PCR技术适用于不同杀虫剂处理间的区分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular Investigation Using RAPD-PCR Marker Field Populations of Pectinophora gossypiella Saunders (Lepidoptera: Gelechiidae) Exposed to Some Insecticide
Seasonally the cotton plant cultivated in Egyptian fields is suffering from the cotton Pink Bollworm Pectinophora gossypiella (Saunders) (Lepidoptera: Gelechiidae) attacking fruits and buds. Insecticide applications reported control failure by the most recommended conventional classes. Monitoring pest DNA changes after sublethal exposure become the new technique to investigate. Then four insecticide treatments were screened by using the molecular marker polymerase chain reaction (PCR) inspection, using four Random amplified polymorphic deoxyribonucleic acid analysis (RAPD-PCR) primers partitioned based on band reproducibility. Result of LC50 was 0.55, 61.1, 69.3, and 0.23 for spinoteram, novaluron, metaflumezone, and dimeuron respectively. The insecticide treatments band of gel produced detected 47 loci ranging from 87 to 63 % polymorphism. The primer efficiency value of PIC =0.361, 0.34, 0.34, 0.355, and 0.262, RP = 5.30, H = 0.473, 0.434, 0.434, 0.462 and 0.31, and MI = 0.10, 0.1386, 0.138, 0.167 and 0.0582 for the same treated samples respectively. Distance and similarity were quantified based on Nei’s and genetic dissimilarity by the UPMGA method then a phylogenetic tree was constructed and grouped the entire genotypes into 2 major clusters and 6 subclusters. The RAPD primers revealed the number of alleles (Na = 0.324, 0.318, 0.318, 0.326, and 0.328), and the effective number of alleles (Ne = 0.571, 0.569, 0.558, 0.574, and 0.5784). The fixation-index (Fst) analysis narrated a very great genetic diversity (Fst = 0.626, 0.684, 0.684, 0.2, and 0.695) exists within the four treated samples respectively. The level of gene flow was (Nm = 0.239, 0.230, 0.230, 0.233, and 0.2187) respectively across the four genotypes studied. Results proved that the RAPD-PCR technique was suitable for distinguishing between insecticide treatments.
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