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Protection of cultured Cyprinus carpio against a lethal viral disease by an attenuated virus vaccine

机译:减毒病毒疫苗对养殖鲤鱼的致死性病毒性疾病的保护

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Massive mortality of koi and common carp--Cyprinus carpio species--has been observed since 1998 in many countries worldwide, resulting in severe economic losses. The cause of the disease is an as yet unclassified large DNA virus, designated carp nephritis gill necrosis virus (CNGV) or koi herpes virus (KHV). Previously, we demonstrated that the wild type CNGV lost its pathogenecity following serial transfer in cell culture, and that clones isolated from the attenuated population can be used as a prophylactic vaccine. Here, we describe the basic conditions required for proper fish immunization so that a protection protocol may be devised. We demonstrated that carps are very sensitive to the pathogenic and the attenuated viruses, and short immersion of fish in water containing the viruses is sufficient for infection. The infection of fish with the pathogenic and the attenuated viruses is temperature-restricted; fish held at the non-permissive temperature, immediately following infection, were not affected by the pathogenic virus, and were not rendered resistant to the disease. Thus, propagation of the virus in the fingerlings is a pre-requisite for immunization. In order to increase the number of random mutations in the genome of the attenuated virus, and thus, reduce the possibility of the attenuated virus reverting to pathogenic, we irradiated it and selected additional clones appropriate for vaccination. The results of our study suggest that a safe and efficient prophylactic vaccine can be developed by selecting an appropriate attenuated virus.
机译:自1998年以来,全世界许多国家都观察到了锦鲤和鲤鱼的大规模死亡,这导致了严重的经济损失。该病的病因是尚未分类的大DNA病毒,称为鲤鱼肾炎g坏死病毒(CNGV)或锦鲤疱疹病毒(KHV)。以前,我们证明了野生型CNGV在细胞培养中连续转移后丧失了其致病性,并且从减毒种群中分离出的克隆可用作预防性疫苗。在这里,我们描述了适当的鱼免疫所需的基本条件,以便可以设计保护方案。我们证明了鲤鱼对致病性病毒和减毒病毒非常敏感,将鱼短时间浸入含有病毒的水中就足以感染。病原性和减毒病毒对鱼类的感染受到温度的限制;感染后立即置于非许可温度下的鱼类不受病原病毒的影响,也没有对这种疾病产生抗药性。因此,病毒在鱼种中的繁殖是免疫的先决条件。为了增加减毒病毒基因组中的随机突变数,从而减少减毒病毒回复到致病性的可能性,我们对其进行了辐照并选择了其他适合疫苗接种的克隆。我们的研究结果表明,可以通过选择适当的减毒病毒来开发安全有效的预防性疫苗。

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