Shao Ying, Ding Jian-Hao, Miao Wang-Long, Wang Yi-Ren, Pei Miao-Miao, Sheng Sheng, Gui Zhong-Zheng
Jiangsu Key Laboratory of Sericultural and Animal Biotechnology, School of Biotechnology, Jiangsu University of Science and Technology, Zhenjiang 212100, China.
Key Laboratory of Silkworm and Mulberry Genetic Improvement, Ministry of Agriculture and Rural Affairs, The Sericultural Research Institute, Chinese Academy of Agricultural Sciences, Zhenjiang 212100, China.
Insects. 2025 May 12;16(5):515. doi: 10.3390/insects16050515.
We first measured the content of chlorfenapyr and tralopyril in silkworm larvae using HPLC, revealing that chlorfenapyr can be biotransformed into tralopyril in silkworms. Then, a differential transcriptomic database of small RNA was constructed through Illumina RNA-Sequencing. qRT-PCR was conducted to determine the expression levels of Bmo-miR-6497-5p and the target CYP450 gene, and Bmo-miR-6497-5p was significantly upregulated in the L3 silkworm larvae 24, 48, and 72 h after they were treated with chlorfenapyr. Furthermore, the target P450 gene was downregulated at these time points. Dual-luciferase validation revealed that the luciferase activity significantly decreased after Bmo-miR-6497-5p bound to . In addition, miRNA mimics/inhibitor injection and bioassays of chlorfenapyr and tralopyril revealed that the mortality of third silkworm larvae injected with the antagomir of Bmo-miR-6497-5p was significantly increased after exposure to a sublethal concentration of chlorfenapyr. These results imply that Bmo-miR-6497-5p targets , regulating its expression. Also, silkworms increase their tolerance to chlorfenapyr by upregulating Bmo-miR-6497-5p expression, thereby inhibiting the biotransformation of chlorfenapyr to toxic tralopyril catalyzed by . The present study reveals the function of microRNA in silkworm tolerance to chlorfenapyr and improves understanding regarding insecticide resistance in Lepidopteran insects.
我们首先使用高效液相色谱法(HPLC)测量了家蚕幼虫中溴虫腈和氯虫酰胺的含量,结果表明溴虫腈在家蚕体内可生物转化为氯虫酰胺。然后,通过Illumina RNA测序构建了小RNA差异转录组数据库。进行qRT-PCR以确定Bmo-miR-6497-5p和靶标CYP450基因的表达水平,在用溴虫腈处理家蚕L3幼虫24、48和72小时后,Bmo-miR-6497-5p显著上调。此外,在这些时间点靶标P450基因下调。双荧光素酶验证表明,Bmo-miR-6497-5p与之结合后,荧光素酶活性显著降低。此外,miRNA模拟物/抑制剂注射以及溴虫腈和氯虫酰胺的生物测定表明,注射Bmo-miR-6497-5p拮抗剂的三龄家蚕幼虫在暴露于亚致死浓度的溴虫腈后死亡率显著增加。这些结果表明Bmo-miR-6497-5p靶向,调节其表达。此外,家蚕通过上调Bmo-miR-6497-5p的表达来提高对溴虫腈的耐受性,从而抑制溴虫腈向由催化产生的有毒氯虫酰胺的生物转化。本研究揭示了微小RNA在家蚕对溴虫腈耐受性中的作用,并增进了对鳞翅目昆虫抗药性的理解。