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首页> 外文期刊>魚病研究 >Duration and Booster Effect of Phylactic Response against White Spot Syndrome Virus Infection in Kuruma Shrimp Orally Administrated with Recombinant Viral Proteins, rVP26 and rVP28
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Duration and Booster Effect of Phylactic Response against White Spot Syndrome Virus Infection in Kuruma Shrimp Orally Administrated with Recombinant Viral Proteins, rVP26 and rVP28

机译:口服重组病毒蛋白,rVP26和rVP28的黑瘤虾对白斑综合症病毒感染的系统反应持续时间和增强效应

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摘要

White spot syndrome virus (WSSV: a synonym of penaeid rod-shaped DNA virus, PRDV) is the causative agent of white spot disease (WSD: penaeid acute viremia, PAV), one of the most serious diseases affecting decapod crustaceans around the world. Recently, "quasi-immune response" was found in kuruma shrimp Penaeus japonicus, wherein individuals that naturally survived from WSD showed protection against a rechallenge with WSSV. The phylaxis against WSSV was also inducible by oral vaccination with recombinant WSSV proteins, rVP26 and rVP28. In the present study, kuruma shrimp orally vaccinated with rVPs were sequentially challenged with WSSV to evaluate onset and duration of phylactic response and booster effect. The phylactic response of shrimp against WSSV-chal-lenge peaked at day 45 after the vaccination with rVP26 (RPS: 100%) and at day 55 with rVP28 (RPS: 93%), and decreased within 10-20 days. The phylaxis against WSSV-challenge was boosted by the secondary vaccination with homologous rVPs, but notby those with heterologous rVPs. The peaks of phylactic responses appeared at day 22 after the secondary vaccination more rapidly than those after the primary vaccination. These results demonstrated that the duration of phylaxis induced by oral vaccination with rVPs was relatively short, but could be extended by booster vaccination with homologous rVPs.
机译:白斑综合症病毒(WSSV:对虾杆状DNA病毒,PRDV的代名词)是白斑病(WSD:对虾急性病毒血症,PAV)的病原体,白斑病是影响全世界十足纲甲壳类动物的最严重疾病之一。最近,在库鲁马虾对虾日本对虾中发现了“准免疫反应”,其中从WSD中自然存活的个体对WSSV的再攻击具有保护作用。还可以通过重组WSSV蛋白rVP26和rVP28口服疫苗来诱导针对WSSV的疾病预防。在本研究中,对口服rVP疫苗的库鲁玛虾按顺序用WSSV攻击,以评估系统反应的发生和持续时间以及增强作用。虾对WSSV-chal-lenge的系统反应在接种rVP26(RPS:100%)的第45天达到峰值,在接种rVP28(RPS:93%)的第55天达到峰值,并在10-20天内下降。同源rVP的二次疫苗接种增强了对WSSV挑战的预防,但异源rVP的疫苗则没有。系统性反应的峰值出现在第二次接种后的第22天比第一次接种后更快。这些结果表明,口服rVPs疫苗诱导的预防疾病的时间相对较短,但可以通过同源rVPs的加强疫苗接种来延长。

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