Boutier Maxime, Gao Yuan, Vancsok Catherine, Suárez Nicolás M, Davison Andrew J, Vanderplasschen Alain
Immunology-Vaccinology, Department of Infectious and Parasitic Diseases, Fundamental and Applied Research for Animals & Health (FARAH), Faculty of Veterinary Medicine, University of Liège, Liège, Belgium.
MRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
Antiviral Res. 2017 Sep;145:60-69. doi: 10.1016/j.antiviral.2017.07.002. Epub 2017 Jul 6.
The genus Cyprinivirus consists of a growing list of phylogenetically related viruses, some of which cause severe economic losses to the aquaculture industry. The archetypal member, cyprinid herpesvirus 3 (CyHV-3) causes mass mortalities worldwide in koi and common carp. A CyHV-3 mutant was described previously that is attenuated in vivo by a deletion affecting two genes (ORF56 and ORF57). The relative contributions of ORF56 and ORF57 to the safety and efficacy profile of this vaccine candidate have now been assessed by analysing viruses individually deleted for ORF56 or ORF57. Inoculation of these viruses into carp demonstrated that the absence of ORF56 did not affect virulence, whereas the absence of ORF57 led to an attenuation comparable to, though slightly less than, that of the doubly deleted virus. To demonstrate further the role of ORF57 as a key virulence factor, a mutant retaining the ORF57 region but unable to express the ORF57 protein was produced by inserting multiple in-frame stop codons into the coding region. Analysis of this virus in vivo revealed a safety and efficacy profile comparable to that of the doubly deleted virus. These findings show that ORF57 encodes an essential CyHV-3 virulence factor. They also indicate that ORF57 orthologues in other cypriniviruses may offer promising targets for the rational design of attenuated recombinant vaccines.
鲤病毒属包含越来越多在系统发育上相关的病毒,其中一些给水产养殖业造成了严重的经济损失。该属的原型成员鲤疱疹病毒3(CyHV-3)在全球范围内导致锦鲤和鲤鱼大量死亡。先前描述了一种CyHV-3突变体,其因影响两个基因(ORF56和ORF57)的缺失而在体内减毒。现在通过分析单独缺失ORF56或ORF57的病毒,评估了ORF56和ORF57对这种候选疫苗安全性和有效性的相对贡献。将这些病毒接种到鲤鱼中表明,缺失ORF56不影响毒力,而缺失ORF57导致减毒程度与双重缺失病毒相当,但略低于双重缺失病毒。为了进一步证明ORF57作为关键毒力因子的作用,通过在编码区插入多个框内终止密码子,产生了一个保留ORF57区域但无法表达ORF57蛋白的突变体。对这种病毒的体内分析显示其安全性和有效性与双重缺失病毒相当。这些发现表明ORF57编码一种必需的CyHV-3毒力因子。它们还表明,其他鲤病毒中的ORF57直系同源物可能为减毒重组疫苗的合理设计提供有前景的靶点。