在夏威夷发现的班达伯格蜜蜂病毒4号基因组的特征

J. Doherty, V. Khadka, Beatrice Kondo, J. Panee
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引用次数: 0

摘要

为了鉴定甜叶菊不同品种的遗传标记,对23种遗传独特的甜叶菊植物的叶片样本进行了RNA测序。出乎意料的是,转录组注释揭示了一个“病毒多蛋白”重叠群,该重叠群被鉴定为Bundaberg Bee Virus 4(BBV4),这是一种以前从未在夏威夷发现过的病毒。在12个样本中发现了BBV4的表达,其表达水平为0.08-339.18个转录本/百万(TPM)。“BBV4 Hawaii”共有序列由227427个读数产生,与来自澳大利亚的BBV4参考样本具有99.7%的同一性。使用三个病毒结构域构建的系统发育树估计将BBV4与伊夫拉维里科的其他成员放在一个单系分支中,支持伊夫拉维里科的分类。发现BBV4基因间区(IGR)在一个预测包含程序性核糖体移位(PRS)所需独特结构的区域内包含一个“滑序列”。BBV4 IGR与另外两种利用替代翻译的小核糖核酸病毒的同源性比较揭示了类似区域的重叠区域。这些结果表明,BBV4可能使用替代翻译,并且其IGR参与了这一过程。这项研究还证明了重新利用具有足够深度覆盖的大型下一代序列(NGS)数据集进行病毒基因组鉴定、量化和表征的实用性。本文的结果代表了BBV4基因组序列的首次完全捕获和世界范围内第二次报告的病毒观察。
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Characterization of Bundaberg Bee Virus 4 Genome Identified in Hawaii
To identify genetic markers of different cultivars of Stevia rebaudiana (stevia), leaf samples from twenty-three genetically unique stevia plants were subjected to RNA sequencing. Unexpectedly, transcriptome annotation revealed a ‘viral polyprotein’ contig, which was identified as the Bundaberg Bee Virus 4 (BBV4), a virus that has not been found in Hawaii before. BBV4 expression was found in twelve samples, and the expression levels ranged from 0.08-339.18 transcripts per million (TPM). A ‘BBV4-Hawaii’ consensus sequence was generated from 227,427 reads and shares 99.7% identity with the BBV4 reference sample from Australia. A phylogenetic tree estimation constructed using three viral domains placed BBV4 in a monophyletic clade with other members of Iflaviridae, supporting an Iflaviridae classification. A BBV4 intergenic region (IGR) was found to contain a ‘slippery sequence’ within a region that is predicted to contain the unique structure required for Programmed Ribosomal Shifting (PRS). A homological comparison of the BBV4 IGR to two other Picornavirales that utilize alternative translation revealed an area of overlap in the analogous regions. These results suggest that BBV4 may utilize alternative translation and that its IGR is involved in the process. This study also demonstrates the utility of repurposing large Next Generation Sequence (NGS) datasets with sufficiently deep coverage for viral genome identification, quantification, and characterization. The results herein represent the first full capture of the BBV4 genomic sequence and the second reported observation of the virus worldwide.
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