Li Ji Lian, Cornman R Scott, Evans Jay D, Pettis Jeffery S, Zhao Yan, Murphy Charles, Peng Wen Jun, Wu Jie, Hamilton Michele, Boncristiani Humberto F, Zhou Liang, Hammond John, Chen Yan Ping
mBio. 2014 Jan 21;5(1):e00898-13. doi: 10.1128/mBio.00898-13.
Emerging and reemerging diseases that result from pathogen host shifts are a threat to the health of humans and their domesticates. RNA viruses have extremely high mutation rates and thus represent a significant source of these infectious diseases. In the present study, we showed that a plant-pathogenic RNA virus, tobacco ringspot virus (TRSV), could replicate and produce virions in honeybees, Apis mellifera, resulting in infections that were found throughout the entire body. Additionally, we showed that TRSV-infected individuals were continually present in some monitored colonies. While intracellular life cycle, species-level genetic variation, and pathogenesis of the virus in honeybee hosts remain to be determined, the increasing prevalence of TRSV in conjunction with other bee viruses from spring toward winter in infected colonies was associated with gradual decline of host populations and winter colony collapse, suggesting the negative impact of the virus on colony survival. Furthermore, we showed that TRSV was also found in ectoparasitic Varroa mites that feed on bee hemolymph, but in those instances the virus was restricted to the gastric cecum of Varroa mites, suggesting that Varroa mites may facilitate the spread of TRSV in bees but do not experience systemic invasion. Finally, our phylogenetic analysis revealed that TRSV isolates from bees, bee pollen, and Varroa mites clustered together, forming a monophyletic clade. The tree topology indicated that the TRSVs from arthropod hosts shared a common ancestor with those from plant hosts and subsequently evolved as a distinct lineage after transkingdom host alteration. This study represents a unique example of viruses with host ranges spanning both the plant and animal kingdoms.
Pathogen host shifts represent a major source of new infectious diseases. Here we provide evidence that a pollen-borne plant virus, tobacco ringspot virus (TRSV), also replicates in honeybees and that the virus systemically invades and replicates in different body parts. In addition, the virus was detected inside the body of parasitic Varroa mites, which consume bee hemolymph, suggesting that Varroa mites may play a role in facilitating the spread of the virus in bee colonies. This study represents the first evidence that honeybees exposed to virus-contaminated pollen could also be infected and raises awareness of potential risks of new viral disease emergence due to host shift events. About 5% of known plant viruses are pollen transmitted, and these are potential sources of future host-jumping viruses. The findings from this study showcase the need for increased surveillance for potential host-jumping events as an integrated part of insect pollinator management programs.
由病原体宿主转移导致的新出现和重新出现的疾病对人类及其家养动物的健康构成威胁。RNA病毒具有极高的突变率,因此是这些传染病的重要来源。在本研究中,我们表明一种植物致病性RNA病毒,烟草环斑病毒(TRSV),能够在蜜蜂(西方蜜蜂)中复制并产生病毒粒子,导致全身感染。此外,我们表明在一些监测的蜂群中持续存在感染TRSV的个体。虽然病毒在蜜蜂宿主中的细胞内生命周期、物种水平的遗传变异和发病机制仍有待确定,但在受感染蜂群中,从春季到冬季TRSV与其他蜜蜂病毒的流行率增加与宿主种群的逐渐减少和冬季蜂群崩溃有关,这表明该病毒对蜂群生存有负面影响。此外,我们表明在以蜜蜂血淋巴为食的体外寄生瓦螨体内也发现了TRSV,但在这些情况下,病毒仅限于瓦螨的胃盲囊,这表明瓦螨可能促进TRSV在蜜蜂中的传播,但不会经历全身感染。最后,我们的系统发育分析表明,来自蜜蜂、蜂花粉和瓦螨的TRSV分离株聚集在一起,形成一个单系分支。树形拓扑结构表明,来自节肢动物宿主的TRSV与来自植物宿主的TRSV有共同的祖先,并且在跨界宿主改变后作为一个独特的谱系进化。这项研究代表了宿主范围跨越植物和动物界的病毒的一个独特例子。
病原体宿主转移是新传染病的主要来源。在这里,我们提供证据表明,一种通过花粉传播的植物病毒,烟草环斑病毒(TRSV),也能在蜜蜂中复制,并且该病毒会全身侵入并在不同身体部位复制。此外,在以蜜蜂血淋巴为食的寄生瓦螨体内检测到了该病毒,这表明瓦螨可能在促进病毒在蜂群中的传播中起作用。这项研究首次证明接触受病毒污染花粉的蜜蜂也可能被感染,并提高了对由于宿主转移事件而出现新病毒疾病的潜在风险的认识。大约5%的已知植物病毒是通过花粉传播的,这些都是未来可能发生宿主跳跃的病毒的潜在来源。这项研究的结果表明,需要加强对潜在宿主跳跃事件的监测,作为昆虫传粉者管理计划的一个组成部分。