DsRNA sequencing revealed a previously missed terminal sequence of a +ssRNA virus that infects dinoflagellate Heterocapsa circularisquama.

IF 1.9 4区 医学 Q3 GENETICS & HEREDITY Virus Genes Pub Date : 2024-02-01 Epub Date: 2024-01-10 DOI:10.1007/s11262-023-02046-3
Michiko Takahashi, Yuichi Masuda, Yuto Chiba, Syun-Ichi Urayama, Keizo Nagasaki
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Abstract

Heterocapsa circularisquama RNA virus (HcRNAV) is the only dinoflagellate-infecting RNA virus cultured. However, only two strains of HcRNAV have been registered with complete genome sequences (strains 34 and 109 for UA and CY types, respectively). To extend the genomic information of HcRNAV, we performed full-genome sequencing of an unsequenced strain of HcRNAV (strain A8) using the fragmented and primer-ligated double-stranded RNA (dsRNA) sequencing (FLDS) method. The complete genome of HcRNAV A8 with 4457 nucleotides (nt) was successfully determined, and sequence alignment of the major capsid protein gene suggested that A8 was a UA-type strain, consistent with its intraspecific host specificity. The complete sequence was found to be 80 nt longer at the 5' terminus than the registered sequences of HcRNAV strains (34 and 109), suggesting that FLDS is more reliable for determining the terminal sequence than conventional methods (5' Rapid Amplification of cDNA End). Our study contributes to a better understanding of dinoflagellate-infecting viruses with limited sequence data.

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DsRNA 测序揭示了一种感染甲藻 Heterocapsa circularisquama 的 +ssRNA 病毒以前遗漏的末端序列。
Heterocapsa circularisquama RNA 病毒(HcRNAV)是唯一培养出的甲藻感染 RNA 病毒。然而,目前仅有两株 HcRNAV 有完整的基因组序列(分别为 UA 型的 34 株和 CY 型的 109 株)。为了扩展 HcRNAV 的基因组信息,我们采用片段和引物连接双链 RNA(dsRNA)测序法(FLDS)对一株未测序的 HcRNAV(A8 株)进行了全基因组测序。成功测定了 HcRNAV A8 的完整基因组,共 4457 个核苷酸(nt),主要帽状蛋白基因的序列比对表明 A8 为 UA 型毒株,与其种内宿主特异性一致。完整序列的 5'末端比 HcRNAV 株系的注册序列(34 和 109)长 80 nt,表明 FLDS 在确定末端序列方面比传统方法(5' cDNA 末端快速扩增法)更可靠。我们的研究有助于更好地了解序列数据有限的甲藻感染病毒。
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来源期刊
Virus Genes
Virus Genes 医学-病毒学
CiteScore
3.30
自引率
0.00%
发文量
76
审稿时长
3 months
期刊介绍: Viruses are convenient models for the elucidation of life processes. The study of viruses is again on the cutting edge of biological sciences: systems biology, genomics, proteomics, metagenomics, using the newest most powerful tools. Huge amounts of new details on virus interactions with the cell, other pathogens and the hosts – animal (including human), insect, fungal, plant, bacterial, and archaeal - and their role in infection and disease are forthcoming in perplexing details requiring analysis and comments. Virus Genes is dedicated to the publication of studies on the structure and function of viruses and their genes, the molecular and systems interactions with the host and all applications derived thereof, providing a forum for the analysis of data and discussion of its implications, and the development of new hypotheses.
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