实时荧光定量PCR检测杀虫剂对棉粉棉铃虫Ace1的诊断性表达

H. Diab
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引用次数: 0

摘要

粉棉铃虫(Pectinophora gossypiella)是埃及棉田的一种破坏性害虫。由于其藏于棉铃内的生物学特性和很少接触杀虫剂的特性,可能会发生防虫失败。因此,在沙尔奇亚省和本尼苏韦夫省的田地里收集的大量虫卵侵染了棉铃。此外,暴露于亚致死浓度的py, Op在实验室生物测定。完成LC50、LC90、斜率、RR的毒性特征。而OP和拟除虫菊酯的共同靶点是乙酰胆碱酯酶。因此,我们采用实时荧光定量PCR的分子标记技术,对编码AChE相对表达的Ace1基因进行了研究,数据生成步骤为RNA分离鉴定、cDNA合成、生成归一化因子,并采用2-ΔΔCT方法对Ct数据进行分析,定量定量杀虫剂处理后提取的幼虫组织的基因表达。数据显示,与对照相比,氯氰菊酯的表达率最高,其次是溴氰菊酯,马拉硫磷和毒死蜱的表达率最低,因此,从ct值来看,杀虫剂的效果以马拉硫磷最高,氯氰菊酯最低。完成了以各种聚类系统和算法为距离测度,结合热图和主成分分析的分层聚类。结果表明,溴氰菊酯和氯氰菊酯处理的基因平均权重较低,是转录稳定的理想内参基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostic expression of the cotton pink bollworm Pectinophora gossypiella (Saunders) Ace1 exposed to some insecticide by the real-time PCR
The Pink Bollworm Pectinophora gossypiella (Saunders) is a devastating pest in Egyptian cotton field. Insecticide control failure may be happen due to its biological features of hide inside bolls and rarely exposed to insecticide application. Thus, a bulk of bolls infested with larvae collected from fields of Sharkia and Benysuef governorate. Moreover, exposed to py, Op sub lethal concentrations in laboratory bioassay. Toxicity features as LC50, LC90 and the slope, and RR was completed. Whereas the common target site of OP and pyrethroid is the acetylcholinesterase enzyme. Thus, the gene Ace1 encoding AChE relative expression was investigated using molecular marker of real-time PCR procedures via the steps of generating data was RNA isolation and characterization, cDNA synthesis, then generating normalization factors, and Ct data attained and analyzed using 2-ΔΔCT method to quantify the gene expression quantitatively of insecticide treated larvae tissue extracted. Data showed the most expressed ratio of samples was cypermethrin followed by deltamethrin compared with the control and the least was malathion and chlorpyrifos, thus, the most effective insecticide was malathion and the least were cypermethrin according to ct values. Hierarchical clustering combined with Heat map and principle component analysis based on various clustering systems and algorithm as distance measures were completed. Validation of reference gene in addition to gene expression stability analyzed by the three optimal gene finders and showed that deltamethrin and cypermethrin treated genes having lower mean weights and considered transcriptionally stable and ideal reference genes.
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