{"title":"Nanosilica inhibits development and reproduction by disrupting juvenile hormone biosynthesis and trehalose metabolism in Mythimna separata ","authors":"Yanmei Jia, Chen Jiang, Yi Yan, Huan Zhang, Lei Zhang, Weixiang Lv","doi":"10.1002/ps.71473","DOIUrl":"https://doi.org/10.1002/ps.71473","url":null,"abstract":"BACKGROUND Nanosilica‐induced plant defense responses against herbivorous pests have been extensively documented, the direct effects of nanosilica on insect development and reproduction, together with the underlying mechanisms, remains largely unknown. In this study, we evaluated the effects of mesoporous silica nanoparticles (MSNs) at three concentrations (50, 100, and 200 mg L <jats:sup>−1</jats:sup> ) on the development, reproduction, and offspring fitness in <jats:italic>Mythimna separata</jats:italic> , a highly destructive migratory pest. RESULTS Here, we found that exposure to all three MSN concentrations significantly reduced larval survival and impaired both larval development and adult reproduction relative to the control. Transgenerational impairment of offspring development and reproduction was also observed, particularly in the 100 and 200 mg L <jats:sup>−1</jats:sup> treatment groups. Transcriptomic analysis and biochemical assays revealed that nanosilica disrupted juvenile hormone (JH) synthesis and trehalose metabolism, leading to lower JH titers, decreased trehalose, glycogen, and triacylglyceride (TAG) contents, smaller lipid droplets, and reduced messenger RNA expression of vitellogenin ( <jats:italic>Vg</jats:italic> ), accompanied by impaired oviposition, including a prolonged preoviposition period, reduced egg production, and a shortened oviposition period. Furthermore, RNA interference‐mediated knockdown of allatotropin ( <jats:italic>AT</jats:italic> ), a key JH biosynthetic gene, significantly decreased JH titers, the levels of trehalose, glycogen, and TAG, and reproductive output through down‐regulating expression of <jats:italic>AT</jats:italic> , <jats:italic>Vg</jats:italic> , and trehalose metabolism genes (including <jats:italic>trehalose</jats:italic> , <jats:italic>glycogenin</jats:italic> ( <jats:italic>GLY</jats:italic> ), <jats:italic>glycogen synthase</jats:italic> ( <jats:italic>GS</jats:italic> ), and <jats:italic>glycogen synthase kinase 3</jats:italic> ( <jats:italic>GSK3</jats:italic> )), suggesting that JH coordinately regulated trehalose metabolism and reproduction in female <jats:italic>M. separata</jats:italic> . <jats:italic>Trehalose</jats:italic> silencing further demonstrated trehalose metabolism directly modulated female reproduction under the condition of nanosilica exposure. CONCLUSIONS Our findings indicate that the JH signaling pathway orchestrates reproductive plasticity in female <jats:italic>M. separata</jats:italic> via trehalose metabolism in response to nanosilica exposure. This advances our understanding of nanosilica‐induced reproductive responses in insects and offer theoretical support for the application of nanosilica in sustainable pest management. © 2026 Society of Chemical Industry.","PeriodicalId":218,"journal":{"name":"Pest Management Science","volume":"501 1","pages":""},"PeriodicalIF":4.1,"publicationDate":"2026-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149374222","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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