Genomic and molecular epidemiological characterization of a novel piscine poxvirus in the red seabream, Pagrus major

IF 1.6 4区 医学 Q3 BIOCHEMICAL RESEARCH METHODS
Naritoyo Ishibashi , Yuri Akase , Shuntaro Watanabe , Hiroshi Yokoyama , Tohru Mekata
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引用次数: 0

Abstract

Since 2020, unexplained mortality has been recorded in a red seabream hatchery. Affected juveniles exhibit skin darkening and sleep-like symptoms, which occasionally cause mass mortality. In this study, we detected a novel poxvirus genome in diseased fish via next-generation sequencing. Transcriptome analysis of moribund individuals revealed multiple contigs with sequence homology to the salmon gill poxvirus, suggesting the presence of a related viral agent. Subsequent metagenomic analysis led to the assembly of a 308-kbp viral genome of a novel piscine poxvirus, designated Japanese seabream poxvirus (JSPV), containing 338 predicted open reading frames. DNA polymerase of JSPV shared 62 and 44 % amino acid identity with those of the salmon gill poxvirus and carp edema virus, respectively. Comparative genomic analysis of piscine poxviruses revealed that genome synteny was highly conserved in the central region. Subsequently, a PCR method was developed and I7L, which encodes the virion core cysteine protease, was successfully detected in all JSPV genogroups. Based on the partial sequence of I7L, JSPV was classified into two major genogroups: I and II. Genogroup I was further subdivided into genogroups Ia and Ib.
红鲷一种新型鱼痘病毒的基因组和分子流行病学特征
自2020年以来,在一个红鲷孵化场记录了无法解释的死亡率。受感染的幼鱼表现出皮肤变黑和类似睡眠的症状,偶尔会导致大量死亡。在这项研究中,我们通过下一代测序在病鱼中检测到一个新的痘病毒基因组。对死亡个体的转录组分析显示多个序列与鲑鱼鳃痘病毒同源,表明存在相关的病毒因子。随后的宏基因组分析导致了一种新型鱼痘病毒的308 kbp病毒基因组的组装,称为日本海痘病毒(JSPV),包含338个预测的开放阅读框。JSPV的DNA聚合酶与鲑鱼鳃痘病毒和鲤鱼水肿病毒的DNA聚合酶氨基酸同源性分别为62%和44% %。对鱼痘病毒的比较基因组分析表明,在中部地区,基因组的合性高度保守。随后,建立了一种PCR方法,成功地在所有JSPV基因群中检测到编码病毒粒子核心半胱氨酸蛋白酶的I7L。根据I7L的部分序列,将JSPV分为I和II两个主要基因群。基因组I进一步细分为基因组Ia和基因组Ib。
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来源期刊
CiteScore
5.80
自引率
0.00%
发文量
209
审稿时长
41 days
期刊介绍: The Journal of Virological Methods focuses on original, high quality research papers that describe novel and comprehensively tested methods which enhance human, animal, plant, bacterial or environmental virology and prions research and discovery. The methods may include, but not limited to, the study of: Viral components and morphology- Virus isolation, propagation and development of viral vectors- Viral pathogenesis, oncogenesis, vaccines and antivirals- Virus replication, host-pathogen interactions and responses- Virus transmission, prevention, control and treatment- Viral metagenomics and virome- Virus ecology, adaption and evolution- Applied virology such as nanotechnology- Viral diagnosis with novelty and comprehensive evaluation. We seek articles, systematic reviews, meta-analyses and laboratory protocols that include comprehensive technical details with statistical confirmations that provide validations against current best practice, international standards or quality assurance programs and which advance knowledge in virology leading to improved medical, veterinary or agricultural practices and management.
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