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β-诺达病毒属抗原多样性的分子基础

Molecular Basis for Antigenic Diversity of Genus Betanodavirus.

作者信息

Panzarin Valentina, Toffan Anna, Abbadi Miriam, Buratin Alessandra, Mancin Marzia, Braaen Stine, Olsen Christel Moræus, Bargelloni Luca, Rimstad Espen, Cattoli Giovanni

机构信息

OIE Reference Laboratory for Viral Encephalopathy and Retinopathy, Department of Comparative Biomedical Sciences, Istituto Zooprofilattico Sperimentale delle Venezie, Legnaro (PD), Italy.

Department of Comparative Biomedicine and Food Science, University of Padua, Legnaro (PD), Italy.

出版信息

PLoS One. 2016 Jul 20;11(7):e0158814. doi: 10.1371/journal.pone.0158814. eCollection 2016.

Abstract

Betanodaviruses are the causative agents of viral nervous necrosis (VNN), a devastating disease for the Mediterranean mariculture. Four different betanodavirus species are recognized, Striped jack-, Redspotted grouper-, Tiger puffer-, and Barfin flounder nervous necrosis virus (SJNNV, RGNNV, TPNNV and BFNNV), but there is little knowledge on their antigenic properties. In order to describe the serological relationships among different betanodavirus genotypes, serum neutralization assays were performed using rabbit polyclonal antisera against eight fish nodaviruses that cover a wide species-, temporal-, spatial- and genetic range. The results indicate that the SJNNV and RGNNV are antigenically distinct, constituting serotypes A and C, respectively. The TPNNV and BFNNV, the latter representing cold-water betanodaviruses, are antigenically related and cluster within serotype B. The reassortant viruses RGNNV/SJNNV and SJNNV/RGNNV group within serotypes A and C, respectively, indicating that the coat protein encoded by RNA2 acts as major immunoreactivity determinant. Immunostaining of in vitro expressed wild type and chimeric capsid proteins between the RGNNV and the SJNNV species indicated that the C-terminal part of the capsid protein retains the immunoreactive portion. The amino acid (aa) residues determining RGNNV and SJNNV antigenic diversity were mapped to aa residues 217-256 and aa 257-341, respectively. Neutralization of reverse genetics derived chimeric viruses indicated that these areas determine the neutralizing epitopes. The data obtained are crucial for the development of targeted serological tests for the diagnosis of VNN, and informative for development of cross-protective vaccines against various betanodavirus genotypes.

摘要

β-诺达病毒是病毒性神经坏死病(VNN)的病原体,这是一种对地中海海水养殖造成毁灭性打击的疾病。已确认有四种不同的β-诺达病毒种类,分别是条石鲷、赤点石斑鱼、虎河豚和条斑星鲽神经坏死病毒(SJNNV、RGNNV、TPNNV和BFNNV),但对它们的抗原特性了解甚少。为了描述不同β-诺达病毒基因型之间的血清学关系,使用针对八种鱼类诺达病毒的兔多克隆抗血清进行了血清中和试验,这些病毒涵盖了广泛的物种、时间、空间和遗传范围。结果表明,SJNNV和RGNNV在抗原性上不同,分别构成血清型A和C。TPNNV和BFNNV(后者代表冷水β-诺达病毒)在抗原性上相关,并聚集在血清型B内。重组病毒RGNNV/SJNNV和SJNNV/RGNNV分别归入血清型A和C,这表明RNA2编码的衣壳蛋白是主要的免疫反应决定因素。对RGNNV和SJNNV物种之间体外表达的野生型和嵌合衣壳蛋白进行免疫染色表明,衣壳蛋白的C末端部分保留了免疫反应部分。确定RGNNV和SJNNV抗原多样性的氨基酸(aa)残基分别定位到aa残基217 - 256和aa 257 - 341。对反向遗传学衍生的嵌合病毒的中和作用表明,这些区域决定了中和表位。所获得的数据对于开发用于诊断VNN的靶向血清学检测至关重要,并且对于开发针对各种β-诺达病毒基因型的交叉保护疫苗具有参考价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f04a/4954670/0c12a70b7aa3/pone.0158814.g001.jpg

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