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利用病毒富集宏基因组学和宏转录组学对圈养和野生袋獾的粪便病毒多样性进行分析。

Fecal Viral Diversity of Captive and Wild Tasmanian Devils Characterized Using Virion-Enriched Metagenomics and Metatranscriptomics.

机构信息

School of Life and Environmental Sciences, University of Sydney, Sydney, New South Wales, Australia.

Marie Bashir Institute for Infectious Diseases and Biosecurity, Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.

出版信息

J Virol. 2019 May 15;93(11). doi: 10.1128/JVI.00205-19. Print 2019 Jun 1.

Abstract

The Tasmanian devil is an endangered carnivorous marsupial threatened by devil facial tumor disease (DFTD). While research on DFTD has been extensive, little is known about viruses in devils and whether any are of potential conservation relevance for this endangered species. Using both metagenomics based on virion enrichment and sequence-independent amplification (virion-enriched metagenomics) and metatranscriptomics based on bulk RNA sequencing, we characterized and compared the fecal viromes of captive and wild devils. A total of 54 fecal samples collected from two captive and four wild populations were processed for virome characterization using both approaches. In total, 24 novel marsupial-related viruses, comprising a sapelovirus, astroviruses, rotaviruses, picobirnaviruses, parvoviruses, papillomaviruses, polyomaviruses, and a gammaherpesvirus, were identified, as well as known mammalian pathogens such as rabbit hemorrhagic disease virus 2. Captive devils showed significantly lower viral diversity than wild devils. Comparison of the two virus discovery approaches revealed substantial differences in the number and types of viruses detected, with metatranscriptomics better suited for RNA viruses and virion-enriched metagenomics largely identifying more DNA viruses. Thus, the viral communities revealed by virion-enriched metagenomics and metatranscriptomics were not interchangeable and neither approach was able to detect all viruses present. An integrated approach using both virion-enriched metagenomics and metatranscriptomics constitutes a powerful tool for obtaining a complete overview of both the taxonomic and functional profiles of viral communities within a sample. The Tasmanian devil is an iconic Australian marsupial that has suffered an 80% population decline due to a contagious cancer, devil facial tumor disease, along with other threats. Until now, viral discovery in this species has been confined to one gammaherpesvirus (dasyurid herpesvirus 2 [DaHV-2]), for which captivity was identified as a significant risk factor. Our discovery of 24 novel marsupial-associated RNA and DNA viruses, and that viral diversity is lower in captive than in wild devils, has greatly expanded our knowledge of gut-associated viruses in devils and provides important baseline information that will contribute to the conservation and captive management of this endangered species. Our results also revealed that a combination of virion-enriched metagenomics and metatranscriptomics may be a more comprehensive approach for virome characterization than either method alone. Our results thus provide a springboard for continuous improvements in the way we study complex viral communities.

摘要

袋獾是一种濒危的肉食性有袋动物,受到恶魔面部肿瘤病(DFTD)的威胁。尽管对 DFTD 的研究已经很广泛,但对袋獾中的病毒知之甚少,也不知道是否有任何病毒对这种濒危物种具有潜在的保护意义。本研究使用基于病毒富集和无序列依赖性扩增的宏基因组学(病毒富集宏基因组学)和基于批量 RNA 测序的宏转录组学,对圈养和野生袋獾的粪便病毒组进行了特征描述和比较。使用这两种方法对来自两个圈养和四个野生种群的 54 个粪便样本进行了病毒组特征描述处理。总共鉴定出了 24 种新型的有袋动物相关病毒,包括一种 sapelovirus、astroviruses、轮状病毒、微小双核糖核酸病毒、细小病毒、乳头瘤病毒、多瘤病毒和一种 γ-疱疹病毒,以及已知的哺乳动物病原体,如兔出血症病毒 2。圈养袋獾的病毒多样性明显低于野生袋獾。两种病毒发现方法的比较显示,检测到的病毒数量和类型存在显著差异,宏转录组学更适合 RNA 病毒,而病毒富集宏基因组学主要鉴定出更多的 DNA 病毒。因此,病毒富集宏基因组学和宏转录组学揭示的病毒群落不能相互替代,两种方法都无法检测到所有存在的病毒。使用病毒富集宏基因组学和宏转录组学的综合方法是获得样本中病毒群落的分类和功能概况的完整概述的有力工具。袋獾是一种标志性的澳大利亚有袋动物,由于一种传染性癌症——恶魔面部肿瘤病(DFTD)以及其他威胁,其数量减少了 80%。到目前为止,对这种物种的病毒发现仅限于一种γ疱疹病毒(袋貂疱疹病毒 2[DaHV-2]),并且已经确定圈养是一个重要的风险因素。我们发现了 24 种新型的有袋动物相关 RNA 和 DNA 病毒,并且圈养袋獾的病毒多样性低于野生袋獾,这极大地扩展了我们对袋獾肠道相关病毒的认识,并为这种濒危物种的保护和圈养管理提供了重要的基线信息。我们的研究结果还表明,病毒富集宏基因组学和宏转录组学的结合可能是一种比单独使用任何一种方法更全面的病毒组特征描述方法。因此,我们的研究结果为我们研究复杂病毒群落的方式提供了一个持续改进的起点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ebb/6532096/a1b0bdbe62da/JVI.00205-19-f0001.jpg

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