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肌肉内和口服接种鲤鱼疱疹病毒 ORF25 DNA 疫苗不能保护鲤鱼(Cyprinus carpio L.)。

Intra-muscular and oral vaccination using a Koi Herpesvirus ORF25 DNA vaccine does not confer protection in common carp (Cyprinus carpio L.).

机构信息

Cell Biology and Immunology Group, Wageningen University, The Netherlands.

Department of Animal Sciences, RH Smith Faculty of Agriculture Food and Environment, The Hebrew University of Jerusalem, Rehovot, Israel.

出版信息

Fish Shellfish Immunol. 2019 Feb;85:90-98. doi: 10.1016/j.fsi.2018.03.037. Epub 2018 Mar 19.

Abstract

Koi Herpes Virus (KHV or Cyprinid Herpesvirus 3, CyHV-3) is among the most threatening pathogens affecting common carp production as well as the highly valuable ornamental koi carp. To date, no effective commercial vaccine is available for worldwide use. A previous study reported that three intramuscular injections with an ORF25-based DNA vaccine, led to the generation of neutralizing antibodies and conferred significant protection against an intraperitoneal challenge with KHV. In the present study, we set out to optimize an ORF25-based DNA vaccination protocol that required fewer injections and would confer protection upon a challenge that better resembled the natural route of infection. To this end, ORF25 was cloned in pcDNA3 either as a soluble protein or as a full-length transmembrane GFP-fusion protein. We tested our ORF25-based DNA vaccines in multiple vaccination trials using different doses, vaccination routes (i.m. injection and oral gavage) and challenge methods (bath and cohabitation). Furthermore, we analysed local and systemic responses to the i.m. injected DNA vaccine through histological and RT-qPCR analysis. We observed a strong protection when fish received three injections of either of the two DNA vaccines. However, this protection was observed only after bath challenge and not after cohabitation challenge. Furthermore, protection was insufficient when fish received one injection only, or received the plasmid orally. The importance of choosing a challenge model that best reflects the natural route of infection and the possibility to include additional antigens in future DNA vaccination strategies against KHV will be discussed.

摘要

锦鲤疱疹病毒(KHV 或鲤鱼疱疹病毒 3,CyHV-3)是对鲤鱼养殖以及高价值观赏锦鲤影响最大的病原体之一。迄今为止,全球尚无有效的商业疫苗。先前的一项研究报告称,通过三次肌肉内注射基于 ORF25 的 DNA 疫苗,可产生中和抗体,并对锦鲤疱疹病毒的腹腔内攻毒提供显著保护。在本研究中,我们着手优化基于 ORF25 的 DNA 疫苗接种方案,该方案需要更少的注射次数,并能在更接近自然感染途径的攻毒中提供保护。为此,ORF25 被克隆到 pcDNA3 中,作为可溶性蛋白或全长跨膜 GFP 融合蛋白。我们使用不同剂量、接种途径(肌肉内注射和口服灌胃)和挑战方法(浴和同居)在多次接种试验中测试了我们基于 ORF25 的 DNA 疫苗。此外,我们通过组织学和 RT-qPCR 分析分析了对肌肉内注射 DNA 疫苗的局部和全身反应。当鱼接受两种 DNA 疫苗中的任何一种三次注射时,我们观察到了强烈的保护作用。然而,这种保护仅在浴式攻毒后观察到,而在同居攻毒后未观察到。此外,当鱼仅接受一次注射或口服质粒时,保护作用不足。选择最能反映自然感染途径的挑战模型以及在未来针对 KHV 的 DNA 疫苗接种策略中包含额外抗原的可能性的重要性将被讨论。

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