Interactive effects of chlorothalonil and Varroa destructor on Apis mellifera during adult stage

IF 4.2 1区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pesticide Biochemistry and Physiology Pub Date : 2024-09-01 DOI:10.1016/j.pestbp.2024.106107
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Abstract

The interaction between environmental factors affecting honey bees is of growing concern due to their potential synergistic effects on bee health. Our study investigated the interactive impact of Varroa destructor and chlorothalonil on workers' survival, fat body morphology, and the expression of gene associated with detoxification, immunity, and nutrition metabolism during their adult stage. We found that both chlorothalonil and V. destructor significantly decreased workers' survival rates, with a synergistic effect observed when bees were exposed to both stressors simultaneously. Morphological analysis of fat body revealed significant alterations in trophocytes, particularly a reduction in vacuoles and granules after Day 12, coinciding with the transition of the bees from nursing to other in-hive work tasks. Gene expression analysis showed significant changes in detoxification, immunity, and nutrition metabolism over time. Detoxification genes, such as CYP9Q2, CYP9Q3, and GST-D1, were downregulated in response to stressor exposure, indicating a potential impairment in detoxification processes. Immune-related genes, including defensin-1, Dorsal-1, and Kayak, exhibited an initially upregulation followed by varied expression patterns, suggesting a complex immune response to stressors. Nutrition metabolism genes, such as hex 70a, AmIlp2, VGMC, AmFABP, and AmPTL, displayed dynamic expression changes, reflecting alterations in nutrient utilization and energy metabolism in response to stressors. Overall, these findings highlight the interactive and dynamic effects of environmental stressor on honey bees, providing insights into the mechanisms underlying honey bee decline. These results emphasize the need to consider the interactions between multiple stressors in honey bee research and to develop management strategies to mitigate their adverse effects on bee populations.

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百菌清和瓦罗虫对成虫阶段的蜜蜂的交互影响
由于环境因素对蜜蜂健康的潜在协同效应,影响蜜蜂的环境因素之间的相互作用日益受到关注。我们的研究调查了百菌清和Varroa destructor对工蜂成虫期存活率、脂肪体形态以及解毒、免疫和营养代谢相关基因表达的交互影响。我们发现,百菌清和V. destructor都会显著降低工蜂的存活率,当蜜蜂同时受到这两种胁迫时,会产生协同效应。脂肪体的形态学分析表明滋养细胞发生了显著变化,特别是第12天后空泡和颗粒减少,这与蜜蜂从哺乳过渡到其他巢内工作任务的时间相吻合。基因表达分析表明,随着时间的推移,解毒、免疫和营养代谢发生了显著变化。CYP9Q2、CYP9Q3和GST-D1等解毒基因在暴露于应激源后出现下调,表明解毒过程可能受到损害。免疫相关基因,包括防御素-1、Dorsal-1 和 Kayak,最初表现出上调,随后表现出不同的表达模式,表明对应激源有复杂的免疫反应。营养代谢基因,如 hex 70a、AmIlp2、VGMC、AmFABP 和 AmPTL,表现出动态的表达变化,反映了营养物质利用和能量代谢在应激反应中的变化。总之,这些发现凸显了环境胁迫对蜜蜂的交互和动态影响,为蜜蜂衰退的内在机制提供了启示。这些结果表明,在蜜蜂研究中需要考虑多种应激源之间的相互作用,并制定管理策略以减轻它们对蜜蜂种群的不利影响。
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来源期刊
CiteScore
7.00
自引率
8.50%
发文量
238
审稿时长
4.2 months
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.
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