Livestock & Aquaculture, CSIRO Agriculture & Food, Queensland Bioscience Precinct, 306 Carmody Road, St. Lucia, QLD, 4067, Australia.
Virus Res. 2021 Jan 15;292:198225. doi: 10.1016/j.virusres.2020.198225. Epub 2020 Nov 9.
Reported here is the complete genome sequence of Mourilyan virus (MoV) that infects giant tiger (Penaeus monodon) and kuruma prawns (P. japonicas) in Australia. Its genome was determined using various PCR strategies based on the sequences of 3 randomly-amplified cDNA clones to its L and M RNA segments discovered in a library generated to determine the genome sequence of gill-associated ronivirus. The sequences of PCR products and clones obtained showed the MoV genome to comprise 4 ssRNA segments (L, M, S1 and S2), as confirmed by Northern blotting using RNA from naïve and MoV-infected prawns, and by Illumina sequence analysis of semi-purified MoV. BLASTn searches identified the MoV L, M and S1 RNA segments to be homologous to Wēnzhōu shrimp virus 1 (WzSV1) segments discovered recently in a P. monodon RNA-Seq library (SRR1745808). Mapping this read library to the MoV S2 RNA segment identified WzSV1 to also possess an equivalent segment. BLASTp searches identified the putative non-structural protein (NSs2; 393-394 aa) encoded in their S2 RNA segments to have no homologs in GenBank. Possibly due to NSs2 being encoded in a discrete RNA segment rather than in ambisense relative to the N protein as in the S RNA segments of other phenuiviruses, each of 6 MoV S1 RNA segment clones sequenced possessed a variable-length (≤ 645 nt) imperfect GA-repeat extending from the N protein stop codon to the more variable ∼90 nt segment terminal sequence. Read mapping of RNA-Seq library SRR1745808 showed the WzSV1 S1 RNA segment to possess a similar GA-repeat. However, paired-read variations hindered definitive assembly of a consensus sequence. All 4 MoV and WzSV1 RNA segments terminated with a 10 nt inverted repeat sequence (5'-ACACAAAGAC.) identical to the RNA segment termini of uukuviruses. Phylogenetic analyses of MoV/WzSV1 RNA-dependant RNA polymerase (L RNA), G1G2 precursor glycoprotein (M RNA) and nucleocapsid (N) protein (S1 RNA) sequences generally clustered them with as yet unassigned crustacean/diptera bunya-like viruses on branches positioned closely to others containing tick-transmitted phenuiviruses. As genome sequences of most phenuiviruses discovered recently have originated from meta-transcriptomics studies, the data presented here showing the MoV and WzSV1 genomes to comprise more than 3 RNA segments, like the plant tenuiviruses, suggests a need to investigate the genomes of these unassigned viruses more closely.
这里报道的是感染澳大利亚巨型虎虾(Penaeus monodon)和斑节对虾(P. japonicas)的 Mourilyan 病毒(MoV)的完整基因组序列。其基因组是通过基于在生成的文库中发现的 3 个随机扩增 cDNA 克隆的 L 和 M RNA 片段的各种 PCR 策略来确定的,该文库旨在确定鳃相关虹彩病毒的基因组序列。通过Northern 印迹分析用来自未感染和 MoV 感染的对虾的 RNA 以及使用 Illumina 对半纯化的 MoV 进行序列分析,证实了 PCR 产物和获得的克隆的序列表明 MoV 基因组由 4 个 ssRNA 片段(L、M、S1 和 S2)组成。BLASTn 搜索鉴定出 MoV 的 L、M 和 S1 RNA 片段与最近在 P. monodon RNA-Seq 文库(SRR1745808)中发现的 Wenzhou 虾病毒 1(WzSV1)片段同源。将该读文库映射到 MoV S2 RNA 片段上,鉴定出 WzSV1 也具有相应的片段。BLASTp 搜索鉴定出它们在 S2 RNA 片段中编码的假定非结构蛋白(NSs2;393-394aa)在 GenBank 中没有同源物。可能由于 NSs2 编码在离散的 RNA 片段中,而不是相对于 N 蛋白在 ambisense 中,如其他 phenuiviruses 的 S RNA 片段,因此测序的 6 个 MoV S1 RNA 片段克隆中的每一个都具有从 N 蛋白终止密码子延伸的可变长度(≤645nt)不完美的 GA-重复序列到更可变的约 90nt 片段末端序列。RNA-Seq 文库 SRR1745808 的读映射显示 WzSV1 S1 RNA 片段具有类似的 GA-重复。然而,配对读的变化阻碍了一致序列的明确组装。所有 4 个 MoV 和 WzSV1 RNA 片段都以 10nt 反向重复序列(5'-ACACAAAGAC.)结尾,与 uukuviruses 的 RNA 片段末端相同。MoV/WzSV1 RNA 依赖性 RNA 聚合酶(L RNA)、G1G2 前体糖蛋白(M RNA)和核衣壳(N)蛋白(S1 RNA)序列的系统发育分析通常将它们与尚未分配甲壳类动物/双翅目 bunya 样病毒聚集在与其他包含 tick-transmitted phenuiviruses 的分支紧密位置。由于最近发现的大多数 phenuiviruses 的基因组序列源自 meta-transcriptomics 研究,因此这里显示的 MoV 和 WzSV1 基因组由 3 个以上 RNA 片段组成,与植物 tenuiviruses 相似,这表明需要更密切地研究这些未分配病毒的基因组。