Imidacloprid and amitraz differentially alter antioxidant enzymes in honeybee (Apis mellifera) hemocytes when exposed to microbial pathogen-associated molecular patterns

IF 8 1区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Science of the Total Environment Pub Date : 2025-03-15 Epub Date: 2025-02-24 DOI:10.1016/j.scitotenv.2025.178868
Dani Sukkar , Lea Wagner , Antoine Bonnefoy , Jairo Falla-Angel , Philippe Laval-Gilly
{"title":"Imidacloprid and amitraz differentially alter antioxidant enzymes in honeybee (Apis mellifera) hemocytes when exposed to microbial pathogen-associated molecular patterns","authors":"Dani Sukkar ,&nbsp;Lea Wagner ,&nbsp;Antoine Bonnefoy ,&nbsp;Jairo Falla-Angel ,&nbsp;Philippe Laval-Gilly","doi":"10.1016/j.scitotenv.2025.178868","DOIUrl":null,"url":null,"abstract":"<div><div>Honeybees (<em>Apis mellifera</em>) are increasingly exposed to pesticides and microbial stressors, yet their combined effects on immune defenses remain unclear. Exposure to the neonicotinoid imidacloprid and the acaricide amitraz, alone and in combination, alters antioxidant enzyme activity in hemocytes when challenged with bacterial components such as lipopolysaccharide and peptidoglycan or the fungal-derived molecule zymosan A. The combination of pesticides with zymosan A synergistically suppresses superoxide dismutase and glutathione-S-transferase activity, while catalase activity remains unchanged. In contrast, lipopolysaccharide counteracts pesticide-induced oxidative stress, suggesting immune-pathway-specific modulation. The heightened vulnerability of honeybees to fungal-associated immune challenges in pesticide-contaminated environments compromises their ability to detoxify harmful substances and respond to infections. Such approaches that include comparison of different microbial interactions, pesticide cocktails, and immunity are needed. Understanding these interactions is essential for improving pesticide regulations and pollinator conservation efforts in the face of increasing environmental stressors.</div></div>","PeriodicalId":422,"journal":{"name":"Science of the Total Environment","volume":"969 ","pages":"Article 178868"},"PeriodicalIF":8.0000,"publicationDate":"2025-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science of the Total Environment","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0048969725005030","RegionNum":1,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/24 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Honeybees (Apis mellifera) are increasingly exposed to pesticides and microbial stressors, yet their combined effects on immune defenses remain unclear. Exposure to the neonicotinoid imidacloprid and the acaricide amitraz, alone and in combination, alters antioxidant enzyme activity in hemocytes when challenged with bacterial components such as lipopolysaccharide and peptidoglycan or the fungal-derived molecule zymosan A. The combination of pesticides with zymosan A synergistically suppresses superoxide dismutase and glutathione-S-transferase activity, while catalase activity remains unchanged. In contrast, lipopolysaccharide counteracts pesticide-induced oxidative stress, suggesting immune-pathway-specific modulation. The heightened vulnerability of honeybees to fungal-associated immune challenges in pesticide-contaminated environments compromises their ability to detoxify harmful substances and respond to infections. Such approaches that include comparison of different microbial interactions, pesticide cocktails, and immunity are needed. Understanding these interactions is essential for improving pesticide regulations and pollinator conservation efforts in the face of increasing environmental stressors.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
当暴露于微生物病原体相关分子模式时,吡虫啉和阿米特嗪会不同地改变蜜蜂血细胞中的抗氧化酶
蜜蜂(Apis mellifera)越来越多地暴露于农药和微生物压力源,但它们对免疫防御的综合影响尚不清楚。暴露于新烟碱类吡虫啉和杀螨剂氨咪唑,单独或联合,当受到细菌成分(如脂多糖、肽聚糖或真菌衍生的分子酶A)的攻击时,改变血细胞中抗氧化酶的活性。农药与酶A的组合协同抑制超氧化物歧化酶和谷胱甘肽- s -转移酶的活性,而过氧化氢酶的活性保持不变。相反,脂多糖抵消农药诱导的氧化应激,提示免疫途径特异性调节。在农药污染的环境中,蜜蜂对真菌相关免疫挑战的脆弱性增加,损害了它们对有害物质解毒和对感染作出反应的能力。这些方法包括比较不同微生物的相互作用、混合杀虫剂和免疫力。了解这些相互作用对于改善农药法规和面对日益增加的环境压力的传粉媒介保护工作至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Science of the Total Environment
Science of the Total Environment 环境科学-环境科学
CiteScore
17.60
自引率
10.20%
发文量
8726
审稿时长
2.4 months
期刊介绍: The Science of the Total Environment is an international journal dedicated to scientific research on the environment and its interaction with humanity. It covers a wide range of disciplines and seeks to publish innovative, hypothesis-driven, and impactful research that explores the entire environment, including the atmosphere, lithosphere, hydrosphere, biosphere, and anthroposphere. The journal's updated Aims & Scope emphasizes the importance of interdisciplinary environmental research with broad impact. Priority is given to studies that advance fundamental understanding and explore the interconnectedness of multiple environmental spheres. Field studies are preferred, while laboratory experiments must demonstrate significant methodological advancements or mechanistic insights with direct relevance to the environment.
期刊最新文献
Impacts of inhaled exposures on the upper respiratory tract microbiome: a systematic review Harnessing fungi and bacteria to speed up the biodegradation of plastic mulch films Continuum of denitrification to end-member controls on nitrate isotopic ratios: evidence from meta-analyses and a six-year record of seasonality from Kentucky, USA Biochemical responses and ingestion of microplastics by native fishes in the Atlantic Forest, southern Brazil Land management controls on snow accumulation in a cold-region agricultural watershed
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1