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除虫菊酯类农药吡丙醚通过抑制昆虫几丁质合成酶 1 表达,延缓了捕食性天敌昆虫八斑球腹蛛的蜕皮。

Buprofezin delayed the molting of Pardosa pseudoannulata, a predatory enemy for insect pests, by suppressing chitin synthase 1 expression.

机构信息

Key Laboratory of Integrated Management of Crop Diseases and Pests (Ministry of Education), College of Plant Protection, Nanjing Agricultural University, Weigang 1, Nanjing 210095, China.

Key Laboratory of Integrated Management of Crop Diseases and Pests (Ministry of Education), College of Plant Protection, Nanjing Agricultural University, Weigang 1, Nanjing 210095, China.

出版信息

Pestic Biochem Physiol. 2024 Feb;199:105798. doi: 10.1016/j.pestbp.2024.105798. Epub 2024 Jan 18.

Abstract

Spiders, the major predatory enemies of insect pests in fields, are vulnerable to insecticides. In this study, we observed that the recommended dose of buprofezin delayed the molting of the pond wolf spider Pardosa pseudoannulata, although it had no lethal effect on the spiders. Since buprofezin is an insect chitin biosynthesis inhibitor, we identified two chitin synthase genes (PpCHS1 and PpCHS2) in P. pseudoannulata. Tissue-specific expression profiling showed that PpCHS1 was most highly expressed in cuticle. In contrast, PpCHS2 showed highest mRNA levels in the midgut and fat body. RNAi knockdown of PpCHS1 significantly delayed the molting of 12-days old spiderlings, whereas no significant effect on the molting was observed in the PpCHS2-silencing spiderlings. The expression of PpCHS1 was significantly suppressed in the spiderlings treated with buprofezin, but rescued by exogenous ecdysteroid ponasterone A (PA). Consistent with this result, the molting delay caused by buprofezin was also rescued by PA. The results revealed that buprofezin delayed the molting of spiders by suppressing PpCHS1 expression, which will benefit the protection of P. pseudoannulate and related spider species.

摘要

蜘蛛是农田中主要的害虫捕食性天敌,对杀虫剂很敏感。在这项研究中,我们观察到,尽管吡丙醚对狼蛛没有致死作用,但推荐剂量的吡丙醚会延迟池塘狼蛛 Pardosa pseudoannulata 的蜕皮。由于吡丙醚是一种昆虫几丁质生物合成抑制剂,我们在 P. pseudoannulata 中鉴定了两个几丁质合酶基因(PpCHS1 和 PpCHS2)。组织特异性表达谱分析表明,PpCHS1 在表皮中表达量最高。相比之下,PpCHS2 在中肠和脂肪体中具有最高的 mRNA 水平。PpCHS1 的 RNAi 敲低显著延迟了 12 天大的幼蛛蜕皮,而 PpCHS2 沉默的幼蛛蜕皮则没有明显影响。吡丙醚处理的幼蛛中 PpCHS1 的表达明显受到抑制,但外源蜕皮甾酮 A (PA) 可以挽救。与这一结果一致,吡丙醚引起的蜕皮延迟也被 PA 挽救。结果表明,吡丙醚通过抑制 PpCHS1 的表达来延迟蜘蛛蜕皮,这将有利于保护 P. pseudoannulate 和相关的蜘蛛物种。

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