Yan Bai, Fengting Kong, Xiaoyu Song, Yafei Han, Yinzhou Jiang, Jiangchun Hu, Huaqi Pan
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{"title":"内生青霉菌brefeldium F4a的吲哚二萜及其对果夜蛾的拒食和杀虫活性","authors":"Yan Bai, Fengting Kong, Xiaoyu Song, Yafei Han, Yinzhou Jiang, Jiangchun Hu, Huaqi Pan","doi":"10.1002/ps.8842","DOIUrl":null,"url":null,"abstract":"BACKGROUND<jats:italic>Spodoptera frugiperda</jats:italic> (Lepidoptera: Noctuidae) is one of the world's major agriculture pests, causing significant crop damage and serious economic losses. As <jats:italic>S. frugiperda</jats:italic> has developed widespread resistance, environmentally friendly insecticides are urgently needed. Therefore, searching for natural antifeedant or insecticidal lead compounds has become imperative.RESULTSThree new indole diterpenoids, paspamine A (1), paspamine B (2), and paspalitrem D (3), along with nine known ones (compounds 4–12), were isolated from an endophytic <jats:italic>Penicillium brefeldianum</jats:italic> F4a. Their structures were identified through comprehensive spectroscopic data analysis [one‐dimensional (1D) and two‐dimensional (2D) nuclear magnetic resonance (NMR), high‐resolution electrospray ionization mass spectrometry (HR‐ESI‐MS), ultraviolet (UV), infrared (IR)], and electronic circular dichroism (ECD) calculations. Furthermore, plausible biosynthetic pathways of these compounds were deduced. The bioassay results indicated that compound 8 displayed more significant antifeedant activity against <jats:italic>S. frugiperda</jats:italic> larvae than azadirachtin and compounds 5–7 demonstrated superior insecticidal activities compared to abamectin. Moreover, comparative transcriptome analysis revealed that compound 6 exerted a distinct insecticidal mechanism. In the early stages, it regulated the expression of genes associated with peptidases and chitinases. Subsequently, this regulation influenced the expression of genes related to cuticle proteins and other relevant genes, ultimately resulting in <jats:italic>S</jats:italic>. <jats:italic>frugiperda</jats:italic> larval death. These results were further confirmed by real‐time quantitative polymerase chain reaction (RT‐qPCR) experiments.CONCLUSIONThis research will provide valuable information for the development of indole diterpenoids as novel microbial insecticides for the management of <jats:italic>S. frugiperda</jats:italic>. © 2025 Society of Chemical Industry.","PeriodicalId":218,"journal":{"name":"Pest Management Science","volume":"17 1","pages":""},"PeriodicalIF":3.8000,"publicationDate":"2025-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Indole‐diterpenoids from an endophytic Penicillium brefeldianum F4a and their antifeedant and insecticidal activities against Spodoptera frugiperda\",\"authors\":\"Yan Bai, Fengting Kong, Xiaoyu Song, Yafei Han, Yinzhou Jiang, Jiangchun Hu, Huaqi Pan\",\"doi\":\"10.1002/ps.8842\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"BACKGROUND<jats:italic>Spodoptera frugiperda</jats:italic> (Lepidoptera: Noctuidae) is one of the world's major agriculture pests, causing significant crop damage and serious economic losses. As <jats:italic>S. frugiperda</jats:italic> has developed widespread resistance, environmentally friendly insecticides are urgently needed. Therefore, searching for natural antifeedant or insecticidal lead compounds has become imperative.RESULTSThree new indole diterpenoids, paspamine A (1), paspamine B (2), and paspalitrem D (3), along with nine known ones (compounds 4–12), were isolated from an endophytic <jats:italic>Penicillium brefeldianum</jats:italic> F4a. Their structures were identified through comprehensive spectroscopic data analysis [one‐dimensional (1D) and two‐dimensional (2D) nuclear magnetic resonance (NMR), high‐resolution electrospray ionization mass spectrometry (HR‐ESI‐MS), ultraviolet (UV), infrared (IR)], and electronic circular dichroism (ECD) calculations. Furthermore, plausible biosynthetic pathways of these compounds were deduced. The bioassay results indicated that compound 8 displayed more significant antifeedant activity against <jats:italic>S. frugiperda</jats:italic> larvae than azadirachtin and compounds 5–7 demonstrated superior insecticidal activities compared to abamectin. Moreover, comparative transcriptome analysis revealed that compound 6 exerted a distinct insecticidal mechanism. In the early stages, it regulated the expression of genes associated with peptidases and chitinases. Subsequently, this regulation influenced the expression of genes related to cuticle proteins and other relevant genes, ultimately resulting in <jats:italic>S</jats:italic>. <jats:italic>frugiperda</jats:italic> larval death. These results were further confirmed by real‐time quantitative polymerase chain reaction (RT‐qPCR) experiments.CONCLUSIONThis research will provide valuable information for the development of indole diterpenoids as novel microbial insecticides for the management of <jats:italic>S. frugiperda</jats:italic>. © 2025 Society of Chemical Industry.\",\"PeriodicalId\":218,\"journal\":{\"name\":\"Pest Management Science\",\"volume\":\"17 1\",\"pages\":\"\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-04-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pest Management Science\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1002/ps.8842\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"AGRONOMY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pest Management Science","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1002/ps.8842","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRONOMY","Score":null,"Total":0}
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Indole‐diterpenoids from an endophytic Penicillium brefeldianum F4a and their antifeedant and insecticidal activities against Spodoptera frugiperda
BACKGROUNDSpodoptera frugiperda (Lepidoptera: Noctuidae) is one of the world's major agriculture pests, causing significant crop damage and serious economic losses. As S. frugiperda has developed widespread resistance, environmentally friendly insecticides are urgently needed. Therefore, searching for natural antifeedant or insecticidal lead compounds has become imperative.RESULTSThree new indole diterpenoids, paspamine A (1), paspamine B (2), and paspalitrem D (3), along with nine known ones (compounds 4–12), were isolated from an endophytic Penicillium brefeldianum F4a. Their structures were identified through comprehensive spectroscopic data analysis [one‐dimensional (1D) and two‐dimensional (2D) nuclear magnetic resonance (NMR), high‐resolution electrospray ionization mass spectrometry (HR‐ESI‐MS), ultraviolet (UV), infrared (IR)], and electronic circular dichroism (ECD) calculations. Furthermore, plausible biosynthetic pathways of these compounds were deduced. The bioassay results indicated that compound 8 displayed more significant antifeedant activity against S. frugiperda larvae than azadirachtin and compounds 5–7 demonstrated superior insecticidal activities compared to abamectin. Moreover, comparative transcriptome analysis revealed that compound 6 exerted a distinct insecticidal mechanism. In the early stages, it regulated the expression of genes associated with peptidases and chitinases. Subsequently, this regulation influenced the expression of genes related to cuticle proteins and other relevant genes, ultimately resulting in S . frugiperda larval death. These results were further confirmed by real‐time quantitative polymerase chain reaction (RT‐qPCR) experiments.CONCLUSIONThis research will provide valuable information for the development of indole diterpenoids as novel microbial insecticides for the management of S. frugiperda . © 2025 Society of Chemical Industry.