Xu Chen, Yu Fangxing, Xue Mingyang, Huang Zhenyu, Jiang Nan, Li Yiqun, Meng Yan, Liu Wenzhi, Zheng Ya, Fan Yuding, Zhou Yong
Yangtze River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Wuhan, China.
College of Life Sciences, Shanghai Normal University, Shanghai, China.
J Virol. 2025 May 20;99(5):e0196024. doi: 10.1128/jvi.01960-24. Epub 2025 Apr 2.
Cyprinid herpesvirus 2 (CyHV-2) is the main pathogen responsible for the development of herpesviral hematopoietic necrosis disease (HVHND) in crucian carp (). The CyHV-2 genome encodes approximately 150 genes that are expressed in a well-defined manner during productive infection. However, CyHV-2 open reading frames (ORFs) are primarily derived from sequence and homology analyses, and most lack protein-level evidence to support their properties. In this study, we used high-resolution mass spectrometry followed by proteogenomic mapping to achieve genome re-annotation of CyHV-2. Based on our results, a total of 1,683 MS/MS spectra could be mapped to the CyHV-2 genome through six-frame translation, with 1,665 corresponding to 117 currently annotated protein-coding ORFs. Three of the remaining 18 peptides were mapped to the N-terminal extension region of known ORFs. However, 12 novel CyHV-2 ORFs, designated nORF1-12, were identified and characterized for the first time based on the remaining 15 peptides that could be mapped to previously unannotated regions of the viral genome. And the sequence differences of the novel phosphorylated nORF1, also referred to as ORF25E, in different CyHV-2 strains indicated that the nORF1 is a prospective molecular marker that can monitor the evolution from the Japan (J) to the China (C) genotype of CyHV-2. These findings further validate existing annotations, expand the genomic landscape of CyHV-2, and provide a rich resource for aquatic virology research.IMPORTANCECyHV-2 is a viral pathogen that poses a significant threat to crucian carp farming. CyHV-2 has a large genome with complex sequence features and diverse coding mechanisms, which complicates accurate genome annotation in the absence of protein-level evidence. Here, we employed various protein extraction and separation methods to increase viral protein coverage and performed an integrated proteogenomic analysis to refine the CyHV-2 genome annotation. A total of 129 viral genes were confidently identified, including 117 currently annotated genes and 12 novel genes. For the first time, we present large-scale evidence of peptide presence and levels in the genome of aquatic viruses and confirm the majority of the predicted proteins in CyHV-2. Our findings enhance the understanding of the CyHV-2 genome structure and provide valuable insights for future studies on CyHV-2 biology.
鲤疱疹病毒2型(CyHV-2)是导致鲫鱼疱疹病毒性造血坏死病(HVHND)的主要病原体。CyHV-2基因组编码约150个基因,这些基因在 productive感染期间以明确的方式表达。然而,CyHV-2开放阅读框(ORF)主要来自序列和同源性分析,大多数缺乏蛋白质水平的证据来支持其特性。在本研究中,我们使用高分辨率质谱联用蛋白质基因组图谱实现了CyHV-2的基因组重新注释。根据我们的结果,通过六框翻译,共有1683个MS/MS谱图可映射到CyHV-2基因组,其中1665个对应于117个当前注释的蛋白质编码ORF。其余18个肽段中有3个映射到已知ORF的N端延伸区域。然而,基于其余15个可映射到病毒基因组先前未注释区域的肽段,首次鉴定并表征了12个新的CyHV-2 ORF,命名为nORF1-12。新的磷酸化nORF1(也称为ORF25E)在不同CyHV-2毒株中的序列差异表明,nORF1是一个潜在的分子标记,可监测CyHV-2从日本(J)基因型到中国(C)基因型的进化。这些发现进一步验证了现有注释,扩展了CyHV-2的基因组图谱,并为水生病毒学研究提供了丰富的资源。
重要性
CyHV-2是一种对鲫鱼养殖构成重大威胁的病毒病原体。CyHV-2具有庞大的基因组,序列特征复杂,编码机制多样,在缺乏蛋白质水平证据的情况下,准确的基因组注释变得复杂。在这里,我们采用了各种蛋白质提取和分离方法来增加病毒蛋白的覆盖率,并进行了综合蛋白质基因组分析以完善CyHV-2的基因组注释。共可靠鉴定出129个病毒基因,包括117个当前注释的基因和12个新基因。我们首次提供了水生病毒基因组中肽段存在和水平的大规模证据,并证实了CyHV-2中大多数预测的蛋白质。我们的发现增强了对CyHV-2基因组结构的理解,并为未来CyHV-2生物学研究提供了有价值的见解。