Abstract

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 Haliotis diversicolor supertexta and OsHV-1 infecting Scapharca broughtonii 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.

Highlights

  • IntroductionWith only a little of their own genetic information, they have evolved to exploit a high diversity of host species across the different branches of the tree of life, from bacteria to eukaryotes, causing diseases with significant impact on host populations [2,3]

  • The combination of short- and long-read HTS revealed that transcriptional strategies of Haliotid herpesvirus-1 (HaHV-1) and Ostreid herpesvirus-1 (OsHV-1) vary substantially, from replication and transcription dynamics to transcript diversity

  • Despite similarities in genome structure, gene, transcript and ORF contents, these we showed that the impact of ADAR hyper-editing on transcripts increased along infecviruses differed substantially in their transcriptional strategies, revealing that each virus–host tion, while the level of transcript the same genes (Figure combination evolved along uniquestrandedness trajectories ondecreased the level offor transcriptome structure and5d)

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Summary

Introduction

With only a little of their own genetic information, they have evolved to exploit a high diversity of host species across the different branches of the tree of life, from bacteria to eukaryotes, causing diseases with significant impact on host populations [2,3]. The double stranded DNA (dsDNA) herpesviruses can infect a variety of hosts, but only two herpesviruses are known to infect invertebrates: Ostreid herpesvirus-1 (OsHV-1) and Haliotid herpesvirus-1 (HaHV-1) [4]. Both cause substantial losses for aquaculture of the Pacific oyster Crassostrea gigas, the blood clam Scapharca broughtonii (OsHV-1), and the abalone Haliotis spp. OsHV-1 and HaHV-1 are distantly related to the other herpesviruses, and constitute a new taxonomic family, Malacoherpesviridae, within the order

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