首页> 外文期刊>Journal of Fish Diseases >Immunity induced by recombinant attenuated IHNV (infectious hematopoietic necrosis virus)-G(N438A) expresses VP2 gene-encoded IPNV (infectious pancreatic necrosis virus) against both pathogens in rainbow trout
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Immunity induced by recombinant attenuated IHNV (infectious hematopoietic necrosis virus)-G(N438A) expresses VP2 gene-encoded IPNV (infectious pancreatic necrosis virus) against both pathogens in rainbow trout

机译:重组衰减IHNV(传染造血坏死病毒)-G(N438A)诱导的免疫表达VP2基因编码的IPNV(传染性胰腺坏死病毒)对彩虹鳟鱼的病原体

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摘要

Infectious hematopoietic necrosis virus (IHNV) and infectious pancreatic necrosis virus (IPNV) are important pathogens in rainbow trout farming worldwide. Their co-infection is also common, which causes great economic loss in juvenile salmon species. Development of a universal virus vaccine providing broadly cross-protective immunity will be of great importance. In this study, we generated two recombinant (r) virus (rIHNV-N438A-Delta NV-EGFP and rIHNV-N438A-Delta NV-VP2) replacing the NV gene of the backbone of rIHNV at the single point mutation at residue 438 with an efficient green fluorescent protein (EGFP) reporter gene and antigenic VP2 gene of IPNV. Meanwhile, we tested their efficacy against the wild-type (wt) IHNV HLJ-09 virus and IPNV serotype Sp virus challenge. The relative per cent survival rates of two recombinant viruses against (wt) IHNV HLJ-09 virus challenge were 84.6% and 81.5%, respectively. Simultaneously, the relative per cent survival rate of rIHNV-N438A-Delta NV-VP2 against IPNV serotype Sp virus challenge was 88.9%. It showed the two recombinant viruses had high protection rates and induced a high level of antibodies against IHNV or IPNV. Taken together, these results suggest the VP2 gene of IPNV can act as candidate gene for vaccine and attenuated multivalent live vaccines and molecular marker vaccines have potential application for viral vaccine.
机译:传染病造血坏死病毒(IHNV)和传染性胰腺坏死病毒(IPNV)是全球彩虹鳟鱼的重要病原体。他们的共同感染也很常见,这导致少年鲑鱼类的经济损失很大。开发普遍的病毒疫苗,提供广泛的交叉保护性免疫力将是非常重要的。在本研究中,我们产生了两种重组(RIHNV-N438A-DELTA NV-EGFP和RIHNV-N438A-DELTA NV-VP2)在残留物438的单点突变中替换RIHNV的骨干的NV基因。高效的绿色荧光蛋白(EGFP)报告基因和IPNV的抗原VP2基因。同时,我们对野生型(WT)IHNV HLJ-09病毒和IPNV血清型SP病毒攻击进行了测试。两种重组病毒对(重组)IHNV HLJ-09病毒攻击的相对百分之率分别为84.6%和81.5%。同时,RIHNV-N438A-DELTA NV-VP2对IPNV血清型SP病毒攻击的相对百分比存活率为88.9%。它显示两种重组病毒具有高保护率,并诱导了对IHNV或IPV的高水平抗体。总之,这些结果表明IPNV的VP2基因可以作为候选基因的疫苗和减毒的多价活疫苗和分子标记疫苗具有潜在的病毒疫苗施用。

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