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采用快速通用方法对传染性鲑鱼贫血病毒不同分离株的全长 3' 和 5' 非翻译基因组区域进行特征描述和比较。

Characterization and comparison of the full 3' and 5' untranslated genomic regions of diverse isolates of infectious salmon anaemia virus by using a rapid and universal method.

机构信息

Marine Scotland, Marine Laboratory, Aberdeen, Scotland, UK.

出版信息

J Virol Methods. 2011 Jun;174(1-2):136-43. doi: 10.1016/j.jviromet.2011.03.023. Epub 2011 Mar 31.

DOI:10.1016/j.jviromet.2011.03.023
PMID:21458495
Abstract

The 3' and 5' untranslated regions (UTRs) of the gene segments of orthomyxoviruses interact closely with the polymerase complex and are important for viral replication and transcription regulation. Despite this, the 3' and 5' RNA UTRs of the infectious salmon anaemia virus (ISAV) genome have only been partially characterized and little is known about the level of conservation between different virus subtypes. This report details for the first time, the adaptation of a rapid method for the simultaneous characterization of the 3' and 5' UTRs of each viral segment of ISAV. This was achieved through self circularization of segments using T4 RNA ligase, followed by PCR and sequencing. Dephosphorylation of 5' ends using tobacco acid pyrophosphatase (TAP) proved to be a specific requirement for ligation of ISAV ends which was not essential for characterization of influenza virus in a similar manner. The development of universal primers facilitated the characterization of 4 genetically distinct ISAV isolates from Canada, Norway and Scotland. Comparison of the UTR regions revealed a similarity in organization and presence of conserved terminal sequences as reported for other orthomyxoviruses. Interestingly, the 3' ends of ISAV segments including segments 1, 5 and 6, were shorter and 5' UTRs generally longer than in their influenza counterparts.

摘要

正粘病毒基因片段的 3' 和 5' 非翻译区(UTR)与聚合酶复合物密切相互作用,对病毒复制和转录调控很重要。尽管如此,传染性鲑鱼贫血病毒(ISAV)基因组的 3' 和 5' RNA UTR 仅部分得到了表征,并且对不同病毒亚型之间的保守程度知之甚少。本报告首次详细介绍了一种快速方法的适应情况,该方法可同时对 ISAV 每个病毒片段的 3' 和 5' UTR 进行特征描述。这是通过使用 T4 RNA 连接酶对片段进行自我环化,然后进行 PCR 和测序来实现的。使用烟草酸焦磷酸酶(TAP)对 5' 端进行去磷酸化被证明是 ISAV 末端连接的特定要求,而这对于以类似方式对流感病毒进行特征描述并不是必需的。通用引物的开发促进了对来自加拿大、挪威和苏格兰的 4 种具有遗传差异的 ISAV 分离株的特征描述。UTR 区域的比较表明,与其他正粘病毒一样,ISAV 的组织和保守末端序列的存在具有相似性。有趣的是,包括 1 、5 和 6 节在内的 ISAV 节的 3' 末端较短,而 5' UTR 通常比其流感病毒对应物长。

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引用本文的文献

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Viruses. 2022 Mar 18;14(3):631. doi: 10.3390/v14030631.
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Development of a reverse genetic system for infectious salmon anemia virus: rescue of recombinant fluorescent virus by using salmon internal transcribed spacer region 1 as a novel promoter.传染性鲑鱼贫血病毒反向遗传系统的开发:利用鲑鱼内部转录间隔区1作为新型启动子拯救重组荧光病毒
Appl Environ Microbiol. 2015 Feb;81(4):1210-24. doi: 10.1128/AEM.03153-14.
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Virtual screening of gene expression regulatory sites in non-coding regions of the infectious salmon anemia virus.
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Structural characterization of the viral and cRNA panhandle motifs from the infectious salmon anemia virus.传染性鲑鱼贫血病毒的病毒和 cRNA 衔接子结构特征。
J Virol. 2011 Dec;85(24):13398-408. doi: 10.1128/JVI.06250-11. Epub 2011 Oct 12.