Tingting Cao , Rongrong Qiu , Jing Chen , Mi Kuang , Keming Wu , Yuxian Xia , Guoxiong Peng
{"title":"苯甲酸埃维菌素和金龟子绿僵菌通过促进真菌致病性来协同增强对后期夜蛾的拮抗作用","authors":"Tingting Cao , Rongrong Qiu , Jing Chen , Mi Kuang , Keming Wu , Yuxian Xia , Guoxiong Peng","doi":"10.1016/j.pestbp.2025.106642","DOIUrl":null,"url":null,"abstract":"<div><div><em>Spodoptera frugiperda</em>, a globally invasive pest, has developed severe resistance to chemical insecticides, necessitating sustainable control strategies. This study investigated the synergistic interaction between emamectin benzoate (EB) and the entomopathogenic fungus <em>Metarhizium anisopliae</em> CQMa421 against fourth-instar larvae. Bioassays revealed a synergistic ratio (SR) of 4.19 when EB was combined with CQMa421 spores (2 × 10<sup>7</sup> spores/mL), reducing EB usage by 76.1 %. CQMa421 did not cause significant effects on <em>S. frugiperda,</em> whereas emamectin benzoate (EB) significantly disrupted feeding, development, and molting, particularly delaying fourth-instar molting by 4.65 days. Compared to EB alone, the combined treatment delayed larval molting by 1.2 days, suppressed feeding (18.3 % reduction in frass weight and 11.1 % weight loss), reduced adult emergence by 12.3 %, shortened oviposition duration by 1.5 days, and decreased total fecundity by 42.5 %. Additionally, the combined treatment increased pupal deformity by 4.4 %, collectively inhibiting population recovery. Mechanistic studies demonstrated that EB accelerated fungal spore germination (GT₅₀ reduced by 3.4 h), appressorium formation (AT₂₅ advanced by 4.5 h), and penetration of the cuticle of <em>Spodoptera frugiperda</em>. Furthermore, the combined treatment significantly downregulated immune-related genes (<em>Attacin</em>: 86.6 %; <em>Cecropin</em>: 61.2 %; <em>MyD88</em>: 50.5 %). This indicates that EB enhances the pathogenicity of the <em>M. anisopliae</em> synergistically by disrupting the host's immune barrier and delaying larval molting. This research provides a strategy and theoretical basis for controlling the resistance of <em>Spodoptera frugiperda</em> through reduced pesticide use and increased effectiveness.</div></div>","PeriodicalId":19828,"journal":{"name":"Pesticide Biochemistry and Physiology","volume":"215 ","pages":"Article 106642"},"PeriodicalIF":4.0000,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synergistic enhancement of emamectin benzoate and Metarhizium anisopliae against late-instar Spodoptera frugiperda by promoting fungal pathogenicity\",\"authors\":\"Tingting Cao , Rongrong Qiu , Jing Chen , Mi Kuang , Keming Wu , Yuxian Xia , Guoxiong Peng\",\"doi\":\"10.1016/j.pestbp.2025.106642\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div><em>Spodoptera frugiperda</em>, a globally invasive pest, has developed severe resistance to chemical insecticides, necessitating sustainable control strategies. This study investigated the synergistic interaction between emamectin benzoate (EB) and the entomopathogenic fungus <em>Metarhizium anisopliae</em> CQMa421 against fourth-instar larvae. Bioassays revealed a synergistic ratio (SR) of 4.19 when EB was combined with CQMa421 spores (2 × 10<sup>7</sup> spores/mL), reducing EB usage by 76.1 %. CQMa421 did not cause significant effects on <em>S. frugiperda,</em> whereas emamectin benzoate (EB) significantly disrupted feeding, development, and molting, particularly delaying fourth-instar molting by 4.65 days. Compared to EB alone, the combined treatment delayed larval molting by 1.2 days, suppressed feeding (18.3 % reduction in frass weight and 11.1 % weight loss), reduced adult emergence by 12.3 %, shortened oviposition duration by 1.5 days, and decreased total fecundity by 42.5 %. Additionally, the combined treatment increased pupal deformity by 4.4 %, collectively inhibiting population recovery. Mechanistic studies demonstrated that EB accelerated fungal spore germination (GT₅₀ reduced by 3.4 h), appressorium formation (AT₂₅ advanced by 4.5 h), and penetration of the cuticle of <em>Spodoptera frugiperda</em>. Furthermore, the combined treatment significantly downregulated immune-related genes (<em>Attacin</em>: 86.6 %; <em>Cecropin</em>: 61.2 %; <em>MyD88</em>: 50.5 %). This indicates that EB enhances the pathogenicity of the <em>M. anisopliae</em> synergistically by disrupting the host's immune barrier and delaying larval molting. This research provides a strategy and theoretical basis for controlling the resistance of <em>Spodoptera frugiperda</em> through reduced pesticide use and increased effectiveness.</div></div>\",\"PeriodicalId\":19828,\"journal\":{\"name\":\"Pesticide Biochemistry and Physiology\",\"volume\":\"215 \",\"pages\":\"Article 106642\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2025-08-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pesticide Biochemistry and Physiology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0048357525003554\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pesticide Biochemistry and Physiology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0048357525003554","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Synergistic enhancement of emamectin benzoate and Metarhizium anisopliae against late-instar Spodoptera frugiperda by promoting fungal pathogenicity
Spodoptera frugiperda, a globally invasive pest, has developed severe resistance to chemical insecticides, necessitating sustainable control strategies. This study investigated the synergistic interaction between emamectin benzoate (EB) and the entomopathogenic fungus Metarhizium anisopliae CQMa421 against fourth-instar larvae. Bioassays revealed a synergistic ratio (SR) of 4.19 when EB was combined with CQMa421 spores (2 × 107 spores/mL), reducing EB usage by 76.1 %. CQMa421 did not cause significant effects on S. frugiperda, whereas emamectin benzoate (EB) significantly disrupted feeding, development, and molting, particularly delaying fourth-instar molting by 4.65 days. Compared to EB alone, the combined treatment delayed larval molting by 1.2 days, suppressed feeding (18.3 % reduction in frass weight and 11.1 % weight loss), reduced adult emergence by 12.3 %, shortened oviposition duration by 1.5 days, and decreased total fecundity by 42.5 %. Additionally, the combined treatment increased pupal deformity by 4.4 %, collectively inhibiting population recovery. Mechanistic studies demonstrated that EB accelerated fungal spore germination (GT₅₀ reduced by 3.4 h), appressorium formation (AT₂₅ advanced by 4.5 h), and penetration of the cuticle of Spodoptera frugiperda. Furthermore, the combined treatment significantly downregulated immune-related genes (Attacin: 86.6 %; Cecropin: 61.2 %; MyD88: 50.5 %). This indicates that EB enhances the pathogenicity of the M. anisopliae synergistically by disrupting the host's immune barrier and delaying larval molting. This research provides a strategy and theoretical basis for controlling the resistance of Spodoptera frugiperda through reduced pesticide use and increased effectiveness.
期刊介绍:
Pesticide Biochemistry and Physiology publishes original scientific articles pertaining to the mode of action of plant protection agents such as insecticides, fungicides, herbicides, and similar compounds, including nonlethal pest control agents, biosynthesis of pheromones, hormones, and plant resistance agents. Manuscripts may include a biochemical, physiological, or molecular study for an understanding of comparative toxicology or selective toxicity of both target and nontarget organisms. Particular interest will be given to studies on the molecular biology of pest control, toxicology, and pesticide resistance.
Research Areas Emphasized Include the Biochemistry and Physiology of:
• Comparative toxicity
• Mode of action
• Pathophysiology
• Plant growth regulators
• Resistance
• Other effects of pesticides on both parasites and hosts.