Bumble Bees and Honey Bees on Islands Harbour Reduced Viral Species Richness, Yet Honey Bee Populations Are Dominated by a Deformed Wing Virus Recombinant.

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jana Dobelmann, Lena Wilfert
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引用次数: 0

Abstract

Pollinators harbour diverse RNA viromes that play a vital role in their health. Yet, factors that shape viral communities are often unclear. The European honey bee (Apis mellifera) is experiencing a viral epidemic since the emergence of the parasitic mite Varroa destructor (varroa) introduced vector-borne transmission, which has also been linked to increased viral spillover into wild pollinator communities. Varroa-free island populations provide natural laboratories to study the effect of varroa, while also allowing us to ask how islands affect viral communities. Barriers that restrict the dispersal of wild pollinators and their pathogens to islands may be overcome by human-mediated transport in managed honey bees. Here we used islands with and without varroa and matched mainland populations of honey bees (A. mellifera) and bumble bees (Bombus terrestris) from 2015 and 2021 to explore how varroa presence and island location affect the virome of managed and wild bees. We find lower viral richness on islands in both species. Bumble bees harbour a distinct viral community that was not affected by varroa but geographically structured. In honey bees, however, varroa-present populations contained more viral reads driven by a high abundance of deformed wing virus (DWV). Within the 6 years between the sampling events, DWV underwent a shift from mostly DWV-B towards a mix of DWV-B and recombinant strains. Surprisingly, these shifts appeared independent of varroa. Viewing pollinator virome composition within an ecological framework provides valuable insights into the barriers to virus spread and could help to predict drivers of disease emergence.

岛屿上的大黄蜂和蜜蜂减少了病毒物种的丰富度,但蜜蜂种群却被一种变形翼病毒重组物所统治。
传粉媒介携带多种RNA病毒,这些病毒对它们的健康起着至关重要的作用。然而,形成病毒群落的因素往往不清楚。欧洲蜜蜂(Apis mellifera)正在经历一场病毒流行,因为寄生性螨虫瓦螨(Varroa destructor,瓦螨)的出现引入了媒介传播,这也与病毒越来越多地外溢到野生传粉昆虫群落有关。没有瓦罗亚的岛屿种群为研究瓦罗亚的影响提供了天然实验室,同时也允许我们询问岛屿如何影响病毒群落。限制野生传粉媒介及其病原体向岛屿传播的障碍可以通过人工介导的管理蜜蜂运输来克服。在这里,我们使用了有和没有瓦罗亚的岛屿,并匹配了2015年和2021年的大陆蜜蜂(A. mellifera)和大黄蜂(Bombus terrestris)种群,以探索瓦罗亚的存在和岛屿位置如何影响管理蜜蜂和野生蜜蜂的病毒群。我们发现两个物种在岛屿上的病毒丰富度较低。大黄蜂拥有一个独特的病毒群落,不受瓦罗亚的影响,但在地理上是有结构的。然而,在蜜蜂中,由高丰度的变形翼病毒(DWV)驱动的varroa-present种群含有更多的病毒读取。在采样事件之间的6年内,DWV经历了从大多数DWV- b向DWV- b和重组菌株的混合转变。令人惊讶的是,这些变化似乎与瓦罗亚无关。在生态框架内观察传粉媒介病毒组组成提供了对病毒传播障碍的宝贵见解,并有助于预测疾病出现的驱动因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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