Key Laboratory of Maricultural Organism Disease Control, Ministry of Agriculture, Qingdao Key Laboratory of Mariculture Epidemiology and Biosecurity, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266237, China.
Laboratory for Marine Fisheries Science and Food Production Processes, Pilot National Laboratory for Marine Science and Technology, Qingdao 266237, China.
Viruses. 2021 Sep 30;13(10):1971. doi: 10.3390/v13101971.
The highly versatile group of Herpesviruses cause disease in a wide range of hosts. In invertebrates, only two herpesviruses are known: the malacoherpesviruses HaHV-1 and OsHV-1 infecting gastropods and bivalves, respectively. To understand viral transcript architecture and diversity we first reconstructed full-length viral genomes of HaHV-1 infecting and OsHV-1 infecting by DNA-seq. We then used RNA-seq over the time-course of experimental infections to establish viral transcriptional dynamics, followed by PacBio long-read sequencing of full-length transcripts to untangle viral transcript architectures at two selected time points. Despite similarities in genome structure, in the number of genes and in the diverse transcriptomic architectures, we measured a ten-fold higher transcript variability in HaHV-1, with more extended antisense gene transcription. Transcriptional dynamics also appeared different, both in timing and expression trends. Both viruses were heavily affected by post-transcriptional modifications performed by ADAR1 affecting sense-antisense gene pairs forming dsRNAs. However, OsHV-1 concentrated these modifications in a few genomic hotspots, whereas HaHV-1 diluted ADAR1 impact by elongated and polycistronic transcripts distributed over its whole genome. These transcriptional strategies might thus provide alternative potential roles for sense-antisense transcription in viral transcriptomes to evade the host's immune response in different virus-host combinations.
疱疹病毒是一组用途广泛的病毒,能感染多种宿主。在无脊椎动物中,仅发现两种疱疹病毒:一种是感染腹足类动物的 Malacoherpesvirus HaHV-1,另一种是感染双壳类动物的 OsHV-1。为了了解病毒转录组的结构和多样性,我们首先通过 DNA 测序对感染 和 的 HaHV-1 进行了全长病毒基因组的重建。然后,我们通过实验感染过程中的 RNA-seq 确定了病毒的转录动力学,随后对两个选定时间点的全长转录本进行了 PacBio 长读测序,以理清病毒转录组的结构。尽管基因组结构、基因数量和转录组结构多样性相似,但我们在 HaHV-1 中测量到了十倍高的转录变异性,具有更长的反义基因转录。转录动力学也有所不同,无论是在时间还是表达趋势上。两种病毒都受到 ADAR1 进行的转录后修饰的严重影响,这些修饰影响形成 dsRNA 的正义-反义基因对。然而,OsHV-1 将这些修饰集中在少数基因组热点上,而 HaHV-1 则通过分布在整个基因组上的伸长和多顺反子转录本来稀释 ADAR1 的影响。因此,这些转录策略可能为病毒转录组中的正义-反义转录提供替代的潜在作用,以在不同的病毒-宿主组合中逃避宿主的免疫反应。