Benjamin J. Hunt , Kumar Saurabh Singh , Bartlomiej J. Troczka , Joanna Mackisack , Emma Randall , Mark Mallott , Tobias Baril , James Galbraith , Bram Kuijper , Ralf Nauen , Alex Hayward , Chris Bass
{"title":"亚致死杀虫剂胁迫改变了害虫桃蚜(Myzus persicae)的灭绝率,但没有改变其基因突变率。","authors":"Benjamin J. Hunt , Kumar Saurabh Singh , Bartlomiej J. Troczka , Joanna Mackisack , Emma Randall , Mark Mallott , Tobias Baril , James Galbraith , Bram Kuijper , Ralf Nauen , Alex Hayward , Chris Bass","doi":"10.1016/j.ibmb.2025.104403","DOIUrl":null,"url":null,"abstract":"<div><div>Insect pests evolve heritable resistance to insecticides through selection acting on genetic variation generated by mutation. It has been hypothesised that exposure to low doses of pesticides may increase mutation rate in pest genomes and accelerate resistance evolution. However, the impact of pesticide-induced stress on the mutation rate of insects has never been empirically tested. Here we leverage new, high-quality genomic resources for the aphid pest <em>Myzus persicae</em> in conjunction with long-term mutation accumulation experiments to interrogate spontaneous genetic and epigenetic mutation rates in insecticide-exposed and unexposed aphid lines. Our data reveal that multigenerational exposure of <em>Myzus persicae</em> to sublethal concentrations of the neonicotinoid insecticide imidacloprid does not increase genetic mutation rate. Rather we show that imidacloprid exposure results in a significantly lower epimutation rate. These findings reveal the rate of origin and composition of (epi)mutations arising in a pest insect and challenge the proposed link between pesticide exposure and the rate of mutation.</div></div>","PeriodicalId":330,"journal":{"name":"Insect Biochemistry and Molecular Biology","volume":"184 ","pages":"Article 104403"},"PeriodicalIF":3.7000,"publicationDate":"2025-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sub-lethal insecticide stress alters epimutation rate but not genetic mutation rate in the pest insect Myzus persicae\",\"authors\":\"Benjamin J. Hunt , Kumar Saurabh Singh , Bartlomiej J. Troczka , Joanna Mackisack , Emma Randall , Mark Mallott , Tobias Baril , James Galbraith , Bram Kuijper , Ralf Nauen , Alex Hayward , Chris Bass\",\"doi\":\"10.1016/j.ibmb.2025.104403\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Insect pests evolve heritable resistance to insecticides through selection acting on genetic variation generated by mutation. It has been hypothesised that exposure to low doses of pesticides may increase mutation rate in pest genomes and accelerate resistance evolution. However, the impact of pesticide-induced stress on the mutation rate of insects has never been empirically tested. Here we leverage new, high-quality genomic resources for the aphid pest <em>Myzus persicae</em> in conjunction with long-term mutation accumulation experiments to interrogate spontaneous genetic and epigenetic mutation rates in insecticide-exposed and unexposed aphid lines. Our data reveal that multigenerational exposure of <em>Myzus persicae</em> to sublethal concentrations of the neonicotinoid insecticide imidacloprid does not increase genetic mutation rate. Rather we show that imidacloprid exposure results in a significantly lower epimutation rate. These findings reveal the rate of origin and composition of (epi)mutations arising in a pest insect and challenge the proposed link between pesticide exposure and the rate of mutation.</div></div>\",\"PeriodicalId\":330,\"journal\":{\"name\":\"Insect Biochemistry and Molecular Biology\",\"volume\":\"184 \",\"pages\":\"Article 104403\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-09-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Insect Biochemistry and Molecular Biology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S096517482500147X\",\"RegionNum\":2,\"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":"Insect Biochemistry and Molecular Biology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S096517482500147X","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Sub-lethal insecticide stress alters epimutation rate but not genetic mutation rate in the pest insect Myzus persicae
Insect pests evolve heritable resistance to insecticides through selection acting on genetic variation generated by mutation. It has been hypothesised that exposure to low doses of pesticides may increase mutation rate in pest genomes and accelerate resistance evolution. However, the impact of pesticide-induced stress on the mutation rate of insects has never been empirically tested. Here we leverage new, high-quality genomic resources for the aphid pest Myzus persicae in conjunction with long-term mutation accumulation experiments to interrogate spontaneous genetic and epigenetic mutation rates in insecticide-exposed and unexposed aphid lines. Our data reveal that multigenerational exposure of Myzus persicae to sublethal concentrations of the neonicotinoid insecticide imidacloprid does not increase genetic mutation rate. Rather we show that imidacloprid exposure results in a significantly lower epimutation rate. These findings reveal the rate of origin and composition of (epi)mutations arising in a pest insect and challenge the proposed link between pesticide exposure and the rate of mutation.
期刊介绍:
This international journal publishes original contributions and mini-reviews in the fields of insect biochemistry and insect molecular biology. Main areas of interest are neurochemistry, hormone and pheromone biochemistry, enzymes and metabolism, hormone action and gene regulation, gene characterization and structure, pharmacology, immunology and cell and tissue culture. Papers on the biochemistry and molecular biology of other groups of arthropods are published if of general interest to the readership. Technique papers will be considered for publication if they significantly advance the field of insect biochemistry and molecular biology in the opinion of the Editors and Editorial Board.