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亚致死剂量氟啶虫胺腈对灰飞虱细胞色素P450的影响
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引用本文:徐鹿,赵春青,徐德进,徐广春,许小龙,顾中言.亚致死剂量氟啶虫胺腈对灰飞虱细胞色素P450的影响.植物保护学报,2017,44(4):679-686
DOI:10.13802/j.cnki.zwbhxb.2017.2016032
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作者单位E-mail
徐鹿 江苏省农业科学院植物保护研究所, 南京 210014  
赵春青 南京农业大学植物保护学院, 南京 210095  
徐德进 江苏省农业科学院植物保护研究所, 南京 210014  
徐广春 江苏省农业科学院植物保护研究所, 南京 210014  
许小龙 江苏省农业科学院植物保护研究所, 南京 210014  
顾中言 江苏省农业科学院植物保护研究所, 南京 210014 zhongyangu@yeah.net 
中文摘要:为明确氟啶虫胺腈对灰飞虱Laodelphax striatellus细胞色素P450的影响,评估其抗药性风险,采用点滴法、酶活力分析法和实时荧光定量PCR法分别测定了氟啶虫胺腈对灰飞虱的毒性及对其细胞色素P450酶活力和P450基因表达量的影响。结果表明,氟啶虫胺腈对灰飞虱的致死中量LD50随着虫龄的增加而升高,1~5龄若虫的LD50为0.10~0.94 ng/头,雌、雄成虫的LD50分别为1.09 ng/头和1.07 ng/头。氟啶虫胺腈对4龄若虫的亚致死剂量LD10、LD30和LD50分别为0.17、0.41、0.76 ng/头,处理灰飞虱4龄若虫后可将其体内P450酶活力分别显著提高1.60、1.97和1.22倍;而各处理响应的P450基因的种类和数量不同,但相对表达量均受到诱导;CYP4DE1CYP426A1CYP303A1CYP4CCYP6FK1CYP6FK171v2的相对表达量表现出时间效应,表达量高峰在处理后24 h或48 h。表明不同亚致死剂量的氟啶虫胺腈在特定时间点可提高相应的细胞色素P450基因表达量,从而使酶蛋白量增加,可能导致灰飞虱体内细胞色素P450酶活力上升。
中文关键词:灰飞虱  氟啶虫胺腈  亚致死剂量  细胞色素P450  基因表达
 
Effects of sublethal sulfoxaflor on cytochrome P450 of the small brown planthopper, Laodelphax striatellus
Author NameAffiliationE-mail
Xu Lu Institute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, Jiangsu Province, China  
Zhao Chunqing College of Plant Protection, Nanjing Agricultural University, Nanjing 210095, Jiangsu Province, China  
Xu Dejin Institute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, Jiangsu Province, China  
Xu Guangchun Institute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, Jiangsu Province, China  
Xu Xiaolong Institute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, Jiangsu Province, China  
Gu Zhongyan Institute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, Jiangsu Province, China zhongyangu@yeah.net 
Abstract:To determine the sublethal effects of sulfoxaflor on cytochrome P450 in small brown planthopper, Laodelphax striatellus, and assess its resistance risk, the topical bioassay was performed to test the acute toxicity of sulfoxaflor on L. striatellus, and enzyme activity assay and real-time PCR assay were adopted to study cytochrome P450 enzyme activity and gene expression changes. Lethal medial dose(LD50)of sulfoxaflor on L. striatellus increased with growth, which was 0.10-0.94 ng per pest on first to fifth instar nymphs, and 1.09 ng per pest and 1.07 ng per pest on female and male adults. Cytochrome P450 enzyme activities of fourth instar nymphs were significantly enhanced by 1.60, 1.97 and 1.22 folds under LD10 (0.17 ng per pest), LD30 (0.41 ng per pest) and LD50 (0.76 ng per pest), respectively. The relative expression levels of different types and numbers of cytochrome P450 genes were increased in response to sublethal sulfoxaflor. The relative expression levels of CYP4DE1, CYP426A1, CYP303A1, CYP4C, CYP6FK1 and CYP6FK171v2 exhibited inducement effects which showed peak at 24 h or 48 h. Sulfoxaflor could significantly increase cytochrome P450 enzyme activity by enhancing multiple cytochrome P450 gene expressions at a particular time point.
keywords:Laodelphax striatellus  sulfoxaflor  sublethal dose  cytochrome P450  gene expression
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