Department of Pathology, University of Cambridge, Cambridge, United Kingdom.
Department of Diagnostic Medicine and Pathobiology, Kansas State University, Manhattan, United States.
Elife. 2022 Feb 28;11:e75668. doi: 10.7554/eLife.75668.
The arterivirus porcine reproductive and respiratory syndrome virus (PRRSV) causes significant economic losses to the swine industry worldwide. Here we apply ribosome profiling (RiboSeq) and parallel RNA sequencing (RNASeq) to characterise the transcriptome and translatome of both species of PRRSV and to analyse the host response to infection. We calculated programmed ribosomal frameshift (PRF) efficiency at both sites on the viral genome. This revealed the nsp2 PRF site as the second known example where temporally regulated frameshifting occurs, with increasing -2 PRF efficiency likely facilitated by accumulation of the PRF-stimulatory viral protein, nsp1β. Surprisingly, we find that PRF efficiency at the canonical ORF1ab frameshift site also increases over time, in contradiction of the common assumption that RNA structure-directed frameshift sites operate at a fixed efficiency. This has potential implications for the numerous other viruses with canonical PRF sites. Furthermore, we discovered several highly translated additional viral ORFs, the translation of which may be facilitated by multiple novel viral transcripts. For example, we found a highly expressed 125-codon ORF overlapping nsp12, which is likely translated from novel subgenomic RNA transcripts that overlap the 3' end of ORF1b. Similar transcripts were discovered for both PRRSV-1 and PRRSV-2, suggesting a potential conserved mechanism for temporally regulating expression of the 3'-proximal region of ORF1b. We also identified a highly translated, short upstream ORF in the 5' UTR, the presence of which is highly conserved amongst PRRSV-2 isolates. These findings reveal hidden complexity in the gene expression programmes of these important nidoviruses.
动脉炎病毒猪繁殖与呼吸综合征病毒(PRRSV)给全球养猪业造成了重大的经济损失。在这里,我们应用核糖体图谱(RiboSeq)和平行 RNA 测序(RNASeq)来描述两种 PRRSV 的转录组和翻译组,并分析宿主对感染的反应。我们计算了病毒基因组上两个位点的程序性核糖体移码(PRF)效率。这揭示了 nsp2 PRF 位点是第二个已知的时间调节移码发生的例子,随着 PRF 刺激病毒蛋白 nsp1β的积累,-2 PRF 效率可能会增加。令人惊讶的是,我们发现,在典型的 ORF1ab 移码位点的 PRF 效率也随着时间的推移而增加,这与 RNA 结构导向的移码位点以固定效率运作的常见假设相矛盾。这对许多具有典型 PRF 位点的其他病毒可能具有潜在影响。此外,我们发现了几个高度翻译的额外病毒 ORF,其翻译可能是由多种新型病毒转录本促进的。例如,我们发现了一个高度表达的 125 个密码子的 ORF 与 nsp12 重叠,它可能是从与 ORF1b 的 3'端重叠的新型亚基因组 RNA 转录本翻译而来。在 PRRSV-1 和 PRRSV-2 中都发现了类似的转录本,这表明在 ORF1b 的 3'近端区域的时间表达方面存在潜在的保守机制。我们还在 5'UTR 中鉴定了一个高度翻译的短上游 ORF,其存在高度保守于 PRRSV-2 分离株。这些发现揭示了这些重要的套式病毒基因表达程序的隐藏复杂性。