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Comparison of Genome Sequences of Single-Stranded RNA Viruses Infecting the Bivalve-Killing Dinoflagellate Heterocapsa circularisquama

机译:单链RNA病毒感染双壳双杀鞭毛鞭毛异鳞茎的基因组序列的比较。

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摘要

Heterocapsa circularisquama RNA virus (HcRNAV) has at least two ecotypes (types UA and CY) that have intraspecies host specificities which are complementary to each other. We determined the complete genomic RNA sequence of two typical HcRNAV strains, HcRNAV34 and HcRNAV109, one of each ecotype. The nucleotide sequences of the viruses were 97.0% similar, and each had two open reading frames (ORFs), ORF-1 coding for a putative polyprotein having protease and RNA-dependent RNA polymerase (RdRp) domains and ORF-2 encoding a single major capsid protein. Phylogenetic analysis of the RdRp amino acid sequence suggested that HcRNAV belongs to a new previously unrecognized virus group. Four regions in ORF-2 had amino acid substitutions when HcRNAV34 was compared to HcRNAV109. We used a reverse transcription-nested PCR system to amplify the corresponding regions and also examined RNAs purified from six other HcRNAV strains with known host ranges. We also looked at natural marine sediment samples. Phylogenetic dendrograms for the amplicons correlated with the intraspecies host specificities of the test virus strains. The cloned sequences found in sediment also exhibited considerable similarities to either the UA-type or CY-type sequence. The tertiary structure of the capsid proteins predicted using computer modeling indicated that many of the amino acid substitutions were located in regions on the outside of the viral capsid proteins. This strongly suggests that the intraspecies host specificity of HcRNAV is determined by nanostructures on the virus surface that may affect binding to suitable host cells. Our study shows that capsid alterations can change the phytoplankton-virus (host-parasite) interactions in marine systems.
机译:圆头异头参RNA病毒(HcRNAV)具有至少两种具有种内宿主特异性且彼此互补的生态型(UA和CY型)。我们确定了两种典型的HcRNAV菌株HcRNAV34和HcRNAV109(每种生态型之一)的完整基因组RNA序列。病毒的核苷酸序列相似性为97.0%,每个都有两个开放阅读框(ORF),ORF-1编码具有蛋白酶和RNA依赖性RNA聚合酶(RdRp)结构域的推定多蛋白,ORF-2编码单个衣壳蛋白。系统发育分析RdRp氨基酸序列表明,HcRNAV属于一个新的以前未被识别的病毒组。将HcRNAV34与HcRNAV109进行比较时,ORF-2中的四个区域具有氨基酸取代。我们使用逆转录嵌套式PCR系统扩增相应区域,还检查了从其他六种已知宿主范围的HcRNAV菌株中纯化的RNA。我们还研究了天然海洋沉积物样本。扩增子的系统发育树状图与测试病毒株的种内宿主特异性相关。在沉积物中发现的克隆序列也表现出与UA型或CY型序列相当的相似性。使用计算机模型预测的衣壳蛋白的三级结构表明,许多氨基酸取代位于病毒衣壳蛋白外部的区域中。这强烈表明,HcRNAV的种内宿主特异性是由病毒表面上的纳米结构决定的,该结构可能影响与合适宿主细胞的结合。我们的研究表明衣壳的改变可以改变海洋系统中浮游植物-病毒(宿主-寄生虫)的相互作用。

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