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细胞色素 P450 和 UDP-糖基转移酶的过度表达与马铃薯甲虫(Leptinotarsa decemlineata)对吡虫啉的抗性有关。

Overexpression of a cytochrome P450 and a UDP-glycosyltransferase is associated with imidacloprid resistance in the Colorado potato beetle, Leptinotarsa decemlineata.

机构信息

Department of Biology, The University of Western Ontario, London, ON, N6A 3K7, Canada.

London Research and Development Centre, Agriculture and Agri-Food Canada, London, ON, N5V 4T3, Canada.

出版信息

Sci Rep. 2017 May 11;7(1):1762. doi: 10.1038/s41598-017-01961-4.

Abstract

Current control of insect pests relies on chemical insecticides, however, insecticide resistance development by pests is a growing concern in pest management. The main mechanisms for insecticide resistance typically involve elevated activity of detoxifying enzymes and xenobiotic transporters that break-down and excrete insecticide molecules. In this study, we investigated the molecular mechanisms of imidacloprid resistance in the Colorado potato beetle, Leptinotarsa decemlineata (Say) (Coleoptera: Chrysomelidae), an insect pest notorious for its capacity to develop insecticide resistance rapidly. We compared the transcriptome profiles of imidacloprid-resistant and sensitive beetle strains and identified 102 differentially expressed transcripts encoding detoxifying enzymes and xenobiotic transporters. Of these, 74 were up-regulated and 28 were down-regulated in the resistant strain. We then used RNA interference to knock down the transcript levels of seven up-regulated genes in the resistant beetles. Ingestion of double-stranded RNA successfully knocked down the expression of the genes for three cytochrome P450s (CYP6BQ15, CYP4Q3 and CYP4Q7), one ATP binding cassette (ABC) transporter (ABC-G), one esterase (EST1), and two UDP-glycosyltransferases (UGT1 and UGT2). Further, we demonstrated that silencing of CYP4Q3 and UGT2 significantly increased susceptibility of resistant beetles to imidacloprid, indicating that overexpression of these two genes contributes to imidacloprid resistance in this resistant strain.

摘要

目前,害虫防治主要依赖于化学杀虫剂,但害虫对杀虫剂的抗药性发展是害虫管理中一个日益严重的问题。杀虫剂抗性的主要机制通常涉及解毒酶和外源性转运蛋白活性的升高,这些酶和蛋白可以分解和排泄杀虫剂分子。在这项研究中,我们研究了抗吡虫啉的马铃薯甲虫(Leptinotarsa decemlineata(Say))(鞘翅目:叶甲科)的分子机制,这种昆虫以快速产生杀虫剂抗性而闻名。我们比较了抗吡虫啉和敏感品系马铃薯甲虫的转录组图谱,鉴定出 102 个编码解毒酶和外源性转运蛋白的差异表达转录本。其中,74 个在抗性品系中上调,28 个下调。然后,我们使用 RNA 干扰敲低了抗性甲虫中 7 个上调基因的转录水平。双链 RNA 的摄入成功敲低了三个细胞色素 P450(CYP6BQ15、CYP4Q3 和 CYP4Q7)、一个 ATP 结合盒(ABC)转运蛋白(ABC-G)、一个酯酶(EST1)和两个 UDP-糖基转移酶(UGT1 和 UGT2)的基因表达。此外,我们证明 CYP4Q3 和 UGT2 的沉默显著增加了抗性甲虫对吡虫啉的敏感性,表明这两个基因的过表达有助于该抗性品系对吡虫啉的抗性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a317/5431904/22fe565e87d6/41598_2017_1961_Fig1_HTML.jpg

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