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变形翅膀病毒在西方蜜蜂中进化起源的多样性。

Evolutionarily diverse origins of deformed wing viruses in western honey bees.

机构信息

Okinawa Institute of Science and Technology, Okinawa 904-0495, Japan.

Department of Entomology, Texas A&M University, College Station, TX 77483.

出版信息

Proc Natl Acad Sci U S A. 2023 Jun 27;120(26):e2301258120. doi: 10.1073/pnas.2301258120. Epub 2023 Jun 20.

DOI:10.1073/pnas.2301258120
PMID:37339224
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10293827/
Abstract

Novel transmission routes can allow infectious diseases to spread, often with devastating consequences. Ectoparasitic varroa mites vector a diversity of RNA viruses, having switched hosts from the eastern to western honey bees ( to ). They provide an opportunity to explore how novel transmission routes shape disease epidemiology. As the principal driver of the spread of deformed wing viruses (mainly DWV-A and DWV-B), varroa infestation has also driven global honey bee health declines. The more virulent DWV-B strain has been replacing the original DWV-A strain in many regions over the past two decades. Yet, how these viruses originated and spread remains poorly understood. Here, we use a phylogeographic analysis based on whole-genome data to reconstruct the origins and demography of DWV spread. We found that, rather than reemerging in western honey bees after varroa switched hosts, as suggested by previous work, DWV-A most likely originated in East Asia and spread in the mid-20th century. It also showed a massive population size expansion following the varroa host switch. By contrast, DWV-B was most likely acquired more recently from a source outside East Asia and appears absent from the original varroa host. These results highlight the dynamic nature of viral adaptation, whereby a vector's host switch can give rise to competing and increasingly virulent disease pandemics. The evolutionary novelty and rapid global spread of these host-virus interactions, together with observed spillover into other species, illustrate how increasing globalization poses urgent threats to biodiversity and food security.

摘要

新型传播途径可使传染病扩散,常带来灾难性后果。寄生性外寄生虫瓦螨传播多种 RNA 病毒,其宿主从东方蜜蜂转换至西方蜜蜂(to)。这为探索新型传播途径如何影响疾病流行病学提供了机会。作为变形翅膀病毒(主要为 DWV-A 和 DWV-B)传播的主要驱动因素,瓦螨感染也推动了全球蜜蜂健康状况的下降。在过去二十年中,毒性更强的 DWV-B 株已在许多地区取代了原始的 DWV-A 株。然而,这些病毒的起源和传播方式仍知之甚少。在这里,我们使用基于全基因组数据的系统地理学分析来重建 DWV 传播的起源和动态。我们发现,与之前的研究表明的相反,DWV-A 最有可能起源于东亚,并在 20 世纪中叶传播。它还显示出在瓦螨宿主转换后大规模种群扩张。相比之下,DWV-B 很可能是最近从东亚以外的来源获得的,并且似乎不存在于原始的瓦螨宿主中。这些结果突出了病毒适应的动态性质,即载体的宿主转换会导致竞争性和日益致命的疾病大流行。这些宿主-病毒相互作用的进化新颖性和快速的全球传播,以及观察到的溢出到其他物种的情况,说明了全球化的加剧如何对生物多样性和粮食安全构成紧迫威胁。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ead/10293827/5c0a0baf2267/pnas.2301258120fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ead/10293827/36bb4aa63e5b/pnas.2301258120fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ead/10293827/5c0a0baf2267/pnas.2301258120fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ead/10293827/36bb4aa63e5b/pnas.2301258120fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ead/10293827/5c0a0baf2267/pnas.2301258120fig02.jpg

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