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表现出毒力差异的传染性胰腺坏死病毒Sp血清型毒株的分子特征分析

Molecular characterization of Sp serotype strains of infectious pancreatic necrosis virus exhibiting differences in virulence.

作者信息

Shivappa R B, Song H, Yao K, Aas-Eng A, Evensen O, Vakharia V N

机构信息

Center for Biosystems Research, University of Maryland Biotechnology Institute and VA-MD Regional College of Veterinary Medicine, University of Maryland, College Park, Maryland 20742, USA.

出版信息

Dis Aquat Organ. 2004 Oct 21;61(1-2):23-32. doi: 10.3354/dao061023.

Abstract

Infectious pancreatic necrosis virus (IPNV), a prototype virus of the family Birnaviridae, exhibits a high degree of antigenic variability, pathogenicity and virulence in salmonid species. The Genomic Segment A encodes all the structural (VP2 and VP3) and nonstructural (NS) proteins, whereas Segment B encodes the viral RNA-dependent RNA polymerase (VP1). We tested 3 different IPNV isolates (Sp103, Sp116 and Sp122) isolated during field outbreaks in Norway for their ability to cause mortality in fry and post-smolt of Atlantic salmon Salmo salar L. The cumulative mortality following experimental challenge in fry was 29% for Sp122 followed by 19% for Sp116 and 15% for Sp103. In post-smolt, the corresponding mortality rates were 79, 46 and 16%, respectively. Comparisons of the deduced amino acid sequences of Segments A and B of all 3 Sp strains revealed substitutions of residues in 13 positions, of which 6 are in VP2, 2 in VP3, and 5 in VP1. Our results suggest that these residues, especially those in the outer capsid VP2, may be involved in the virulence of IPNV. Genome Segment A of the Sp serotype is 3097 nucleotides long and contains a major open reading frame (ORF) encoding a polyprotein of 972 amino acids, which initiates at the second in-frame start codon at Position 119. This was ascertained by making mutants of Segment A clone using site-directed mutagenesis, followed by in vitro transcription-coupled translation reaction and immunoprecipitation analyses. In addition, Segment A also encodes a 15 kDa arginine-rich non-structural protein from a small ORF, preceding and partially overlapping the polyprotein ORF, which is truncated to 12 kDa in the virulent Sp122 strain. Moreover, Segment A could encode a novel, putative 25 kDa protein from another ORF between VP2 and VP4 coding regions, which is only detected in the Sp serotype. Segment B is 2777 nucleotides long and encodes in a single large ORF (a polypeptide of 844 amino acid residues), VP1.

摘要

传染性胰腺坏死病毒(IPNV)是双RNA病毒科的原型病毒,在鲑科鱼类中表现出高度的抗原变异性、致病性和毒力。基因组A片段编码所有结构蛋白(VP2和VP3)和非结构蛋白(NS),而B片段编码病毒RNA依赖的RNA聚合酶(VP1)。我们检测了在挪威野外疫情爆发期间分离出的3种不同的IPNV分离株(Sp103、Sp116和Sp122)对大西洋鲑(Salmo salar L.)鱼苗和后幼鲑的致死能力。鱼苗经实验性攻毒后的累计死亡率,Sp122为29%,其次Sp116为19%,Sp103为15%。在后幼鲑中,相应的死亡率分别为79%、46%和16%。对所有3种Sp株A和B片段推导的氨基酸序列进行比较,发现13个位置的残基有替换,其中6个在VP2中,2个在VP3中,5个在VP1中。我们的结果表明,这些残基,尤其是外衣壳VP2中的残基,可能与IPNV的毒力有关。Sp血清型的基因组A片段长3097个核苷酸,包含一个主要开放阅读框(ORF),编码一个972个氨基酸的多蛋白,该多蛋白从第119位的第二个符合读框的起始密码子开始。这是通过使用定点诱变技术构建A片段克隆的突变体,然后进行体外转录偶联翻译反应和免疫沉淀分析来确定的。此外,A片段还从小开放阅读框编码一种15 kDa富含精氨酸的非结构蛋白,该小开放阅读框位于多蛋白ORF之前并部分重叠,在强毒株Sp122中截短为12 kDa。此外,A片段可从VP2和VP4编码区之间的另一个ORF编码一种新的假定25 kDa蛋白,该蛋白仅在Sp血清型中检测到。B片段长2777个核苷酸,在一个单一的大开放阅读框(一个844个氨基酸残基的多肽)中编码VP1。

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