{"title":"Dietary lipids shape honey bee (Apis mellifera) feeding and resilience to pesticide stress","authors":"Jaya Sravanthi Mokkapati, Christina M. Grozinger","doi":"10.1016/j.jinsphys.2026.105021","DOIUrl":null,"url":null,"abstract":"<div><div>Pesticides are important for crop production but can have negative impacts on beneficial insects such as pollinators. In insects, physiological lipid stores may serve to sequester pesticides, while pesticide metabolism and detoxification often involve fatty acid pathways. Previous studies in <em>Apis mellifera</em> found that honey bees fed pollen with a specific protein-to-lipid ratio had improved survival when exposed to an insecticide. Here, we comprehensively investigate whether and how the type of dietary fat influences survival, energy reserves, and enzymatic biomarkers, following exposure to an organophosphate insecticide, chlorpyrifos. Newly emerged bees were fed protein-based diets enriched with either saturated (SFA), monounsaturated (MUFA), or polyunsaturated fatty acids (PUFA) for 5 days and then exposed orally to chlorpyrifos (at LC₅₀). Bees fed MUFA and PUFA diets consumed significantly more food than those fed SFA-supplemented diet, indicating a clear preference for unsaturated fats. However, under chlorpyrifos exposure, only PUFA-fed bees exhibited significantly higher survival rates, and also maintained greater lipid reserves and acetylcholine esterase activity compared to SFA- and MUFA-fed groups. These results suggest that PUFA-enriched diets may mitigate pesticide toxicity by preserving neural enzyme function and energy homeostasis. No significant changes in glutathione-S-transferase activity were observed across treatments, suggesting limited dietary modulation of this detoxification pathway. Collectively, our findings demonstrate that dietary fatty acid composition influences honey bee physiological resilience to chlorpyrifos and highlight the potential for PUFA-based nutritional interventions or the design of pollinator habitats, to improve resilience to pesticides.</div></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"172 ","pages":"Article 105021"},"PeriodicalIF":2.6000,"publicationDate":"2026-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of insect physiology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022191026000946","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/6/26 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Pesticides are important for crop production but can have negative impacts on beneficial insects such as pollinators. In insects, physiological lipid stores may serve to sequester pesticides, while pesticide metabolism and detoxification often involve fatty acid pathways. Previous studies in Apis mellifera found that honey bees fed pollen with a specific protein-to-lipid ratio had improved survival when exposed to an insecticide. Here, we comprehensively investigate whether and how the type of dietary fat influences survival, energy reserves, and enzymatic biomarkers, following exposure to an organophosphate insecticide, chlorpyrifos. Newly emerged bees were fed protein-based diets enriched with either saturated (SFA), monounsaturated (MUFA), or polyunsaturated fatty acids (PUFA) for 5 days and then exposed orally to chlorpyrifos (at LC₅₀). Bees fed MUFA and PUFA diets consumed significantly more food than those fed SFA-supplemented diet, indicating a clear preference for unsaturated fats. However, under chlorpyrifos exposure, only PUFA-fed bees exhibited significantly higher survival rates, and also maintained greater lipid reserves and acetylcholine esterase activity compared to SFA- and MUFA-fed groups. These results suggest that PUFA-enriched diets may mitigate pesticide toxicity by preserving neural enzyme function and energy homeostasis. No significant changes in glutathione-S-transferase activity were observed across treatments, suggesting limited dietary modulation of this detoxification pathway. Collectively, our findings demonstrate that dietary fatty acid composition influences honey bee physiological resilience to chlorpyrifos and highlight the potential for PUFA-based nutritional interventions or the design of pollinator habitats, to improve resilience to pesticides.
农药对作物生产很重要,但也会对传粉昆虫等有益昆虫产生负面影响。在昆虫体内,生理脂质储存可能起到隔离农药的作用,而农药的代谢和解毒往往涉及脂肪酸途径。先前对蜜蜂的研究发现,当蜜蜂接触杀虫剂时,喂食具有特定蛋白质与脂肪比例的花粉可以提高蜜蜂的存活率。在这里,我们全面研究了暴露于有机磷杀虫剂毒死蜱后,饮食脂肪类型是否以及如何影响生存、能量储备和酶生物标志物。新出现的蜜蜂被喂食富含饱和(SFA),单不饱和(MUFA)或多不饱和脂肪酸(PUFA)的蛋白质饮食5 天,然后口服毒死蜱(在LC₅0)。喂食MUFA和PUFA饮食的蜜蜂比喂食sfa补充饮食的蜜蜂消耗的食物明显更多,这表明蜜蜂对不饱和脂肪有明显的偏好。然而,在毒死蜱暴露下,与SFA和mufa相比,只有pufa喂养的蜜蜂表现出更高的存活率,并且保持了更高的脂质储备和乙酰胆碱酯酶活性。这些结果表明,富含pufa的饲料可能通过保持神经酶功能和能量稳态来减轻农药毒性。不同处理的谷胱甘肽- s -转移酶活性没有显著变化,表明饮食对这一解毒途径的调节有限。总的来说,我们的研究结果表明,膳食脂肪酸组成影响蜜蜂对毒死蜱的生理适应能力,并强调了基于pufa的营养干预或传粉媒介栖息地设计的潜力,以提高对农药的适应能力。
期刊介绍:
All aspects of insect physiology are published in this journal which will also accept papers on the physiology of other arthropods, if the referees consider the work to be of general interest. The coverage includes endocrinology (in relation to moulting, reproduction and metabolism), pheromones, neurobiology (cellular, integrative and developmental), physiological pharmacology, nutrition (food selection, digestion and absorption), homeostasis, excretion, reproduction and behaviour. Papers covering functional genomics and molecular approaches to physiological problems will also be included. Communications on structure and applied entomology can be published if the subject matter has an explicit bearing on the physiology of arthropods. Review articles and novel method papers are also welcomed.