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噻虫嗪(一种新烟碱类杀虫剂)的代谢及其与慢性蜜蜂麻痹病毒在蜜蜂中的相互作用。

Metabolisation of thiamethoxam (a neonicotinoid pesticide) and interaction with the Chronic bee paralysis virus in honeybees.

机构信息

ANSES Sophia Antipolis, Unit of Honeybee Pathology, 105, Route des Chappes, 06902 Sophia-Antipolis, France; INRA PACA, UR 406 Abeilles et Environnement, Site Agroparc, 84914 Avignon, France.

ANSES Sophia Antipolis, Unit of Honeybee Pathology, 105, Route des Chappes, 06902 Sophia-Antipolis, France.

出版信息

Pestic Biochem Physiol. 2018 Jan;144:10-18. doi: 10.1016/j.pestbp.2017.10.009. Epub 2017 Oct 23.

DOI:10.1016/j.pestbp.2017.10.009
PMID:29463403
Abstract

Pathogens and pesticides are likely to co-occur in honeybee hives, but much remains to be investigated regarding their potential interactions. Here, we first investigated the metabolisation kinetics of thiamethoxam in chronically fed honeybees. We show that thiamethoxam, at a dose of 0.25ng/bee/day, is quickly and effectively metabolised into clothianidin, throughout a 20day exposure period. Using a similar chronic exposure to pesticide, we then studied, in a separate experiment, the impact of thiamethoxam and Chronic bee paralysis virus (CBPV) co-exposure in honeybees. The honeybees were exposed to the virus by contact, mimicking the natural transmission route in the hive. We demonstrate that a high dose of thiamethoxam (5.0ng/bee/day) can cause a synergistic increase in mortality in co-exposed honeybees after 8 to 10days of exposure, with no increase in viral loads. At a lower dose (2.5ng/bee/day), there was no synergistic increase of mortality, but viral loads were significantly higher in naturally dead honeybees, compared with sacrificed honeybees exposed to the same conditions. These results show that the interactions between pathogens and pesticides in honeybees can be complex: increasing pesticide doses may not necessarily be linked to a rise in viral loads, suggesting that honeybee tolerance to the viral infection might change with pesticide exposure.

摘要

病原体和杀虫剂很可能同时存在于蜜蜂蜂箱中,但它们之间的潜在相互作用仍有许多待研究。在这里,我们首先研究了噻虫嗪在慢性喂养的蜜蜂中的代谢动力学。我们表明,噻虫嗪在 20 天的暴露期内,以 0.25ng/蜂/天的剂量,快速而有效地代谢成噻虫胺。使用类似的慢性杀虫剂暴露实验,我们在另一个实验中研究了噻虫嗪和慢性麻痹病毒(CBPV)在蜜蜂中的共同暴露的影响。蜜蜂通过接触暴露于病毒,模拟了蜂箱中病毒的自然传播途径。我们证明,高剂量的噻虫嗪(5.0ng/蜂/天)在暴露 8-10 天后,可协同增加共同暴露的蜜蜂的死亡率,而病毒载量没有增加。在较低剂量(2.5ng/蜂/天)下,死亡率没有协同增加,但与暴露于相同条件下的被牺牲的蜜蜂相比,自然死亡的蜜蜂中的病毒载量显著更高。这些结果表明,蜜蜂中病原体和杀虫剂之间的相互作用可能很复杂:增加杀虫剂剂量不一定与病毒载量的增加相关,这表明蜜蜂对病毒感染的耐受性可能会随着杀虫剂暴露而改变。

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