RNA-seq of HaHV-1-infected abalones reveals a common transcriptional signature of Malacoherpesviruses
文献类型: 外文期刊
第一作者: Bai, Chang-Ming
作者: Bai, Chang-Ming;Li, Ya-Nan;Zhang, Shu-Min;Xin, Lu-Sheng;Wang, Chong-Ming;Bai, Chang-Ming;Li, Ya-Nan;Zhang, Shu-Min;Xin, Lu-Sheng;Wang, Chong-Ming;Bai, Chang-Ming;Li, Ya-Nan;Zhang, Shu-Min;Xin, Lu-Sheng;Wang, Chong-Ming;Rosani, Umberto;Li, Ya-Nan;Zhang, Shu-Min
作者机构:
期刊名称:SCIENTIFIC REPORTS ( 影响因子:4.379; 五年影响因子:5.133 )
ISSN: 2045-2322
年卷期: 2019 年 9 卷
页码:
收录情况: SCI
摘要: Haliotid herpesvirus-1 (HaHV-1) is the viral agent causative of abalone viral ganglioneuritis, a disease that has severely affected gastropod aquaculture. Although limited, the sequence similarity between HaHV-1 and Ostreid herpesvirus-1 supported the assignment of both viruses to Malacoherpesviridae, a Herpesvirales family distantly related with other viruses. In this study, we reported the first transcriptional data of HaHV-1, obtained from an experimental infection of Haliotis diversicolor supertexta. We also sequenced the genome draft of the Chinese HaHV-1 variant isolated in 2003 (HaHV-1-CN2003) by PacBio technology. Analysis of 13 million reads obtained from 3 RNA samples at 60 hours post injection (hpi) allowed the prediction of 51 new ORFs for a total of 117 viral genes and the identification of 207 variations from the reference genome, consisting in 135 Single Nucleotide Polymorphisms (SNPs) and 72 Insertions or Deletions (InDels). The pairing of genomic and transcriptomic data supported the identification of 60 additional SNPs, representing viral transcriptional variability and preferentially grouped in hotspots. The expression analysis of HaHV-1 ORFs revealed one putative secreted protein, two putative capsid proteins and a possible viral capsid protease as the most expressed genes and demonstrated highly synchronized viral expression patterns of the 3 infected animals at 60 hpi. Quantitative reverse transcription data of 37 viral genes supported the burst of viral transcription at 30 and 60 hpi during the 72 hours of the infection experiment, and allowed the distinction between early and late viral genes.
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