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贝波特:用于传粉者-病毒感染高通量分析的工具。

Beeporter: Tools for high-throughput analyses of pollinator-virus infections.

机构信息

Bee Research Laboratory, USDA-ARS Agricultural Research Service, Beltsville, Maryland, USA.

出版信息

Mol Ecol Resour. 2022 Apr;22(3):978-987. doi: 10.1111/1755-0998.13526. Epub 2021 Oct 20.

Abstract

Pollinators are in decline thanks to the combined stresses of disease, pesticides, habitat loss, and climate. Honey bees face numerous pests and pathogens but arguably none are as devastating as Deformed wing virus (DWV). Understanding host-pathogen interactions and virulence of DWV in honey bees is slowed by the lack of cost-effective high-throughput screening methods for viral infection. Currently, analysis of virus infection in bees and their colonies is tedious, requiring a well-equipped molecular biology laboratory and the use of hazardous chemicals. Here we describe virus clones tagged with green fluorescent protein (GFP) or nanoluciferase (nLuc) that provide high-throughput detection and quantification of virus infections. GFP fluorescence is measured noninvasively in living bees via commonly available long-wave UV light sources and a smartphone camera, or a standard ultraviolet transilluminator gel imaging system. Nonlethal monitoring with GFP allows continuous screening of virus growth and serves as a direct breeding tool for identifying honey bee parents with increased antiviral resistance. Expression using the nLuc reporter strongly correlates with virus infection levels and is especially sensitive. Using multiple reporters, it is also possible to visualize competition, differential virulence, and host tissue targeting by co-occuring pathogens. Finally, it is possible to directly assess the risk of cross-species "spillover" from honey bees to other pollinators and vice versa.

摘要

由于疾病、农药、栖息地丧失和气候变化的综合压力,传粉媒介正在减少。蜜蜂面临着许多害虫和病原体,但没有一种像变形翅膀病毒 (DWV) 那样具有破坏性。由于缺乏经济高效的高通量筛选病毒感染的方法,因此对蜜蜂宿主-病原体相互作用和 DWV 毒力的理解受到了阻碍。目前,对蜜蜂及其群体中病毒感染的分析既繁琐,又需要配备齐全的分子生物学实验室,并使用危险化学品。在这里,我们描述了用绿色荧光蛋白 (GFP) 或纳米荧光素酶 (nLuc) 标记的病毒克隆,这些克隆可提供高通量检测和定量病毒感染。通过常用的长波紫外线光源和智能手机摄像头或标准紫外线透射仪凝胶成像系统,可在活体蜜蜂中进行 GFP 荧光的非侵入性测量。GFP 的非致死性监测允许对病毒生长进行连续筛选,并可作为识别具有抗病毒抗性增强的蜜蜂亲本的直接育种工具。使用 nLuc 报告基因进行表达与病毒感染水平强烈相关,且特别敏感。使用多个报告基因,还可以可视化共存病原体的竞争、差异毒力和宿主组织靶向。最后,还可以直接评估从蜜蜂到其他传粉媒介的跨物种“溢出”的风险,反之亦然。

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