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首页> 外文期刊>Scientific reports. >A novel Schmallenberg virus subunit vaccine candidate protects IFNAR -/- mice against virulent SBV challenge
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A novel Schmallenberg virus subunit vaccine candidate protects IFNAR -/- mice against virulent SBV challenge

机译:一种新的Schmallenberg病毒亚基疫苗候选候选IFNAR - / - 小鼠免受毒性的SBV挑战

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摘要

Schmallenberg virus (SBV), an arthropod-transmitted pathogenic bunyavirus, continues to be a threat to the European livestock industry, causing morbidity and mortality among young ruminant livestock. Here, we describe a novel SBV subunit vaccine, based on bacterially expressed SBV nucleoprotein (SBV-N) administered with a veterinary-grade Saponin adjuvant. When assayed in an IFNAR-/- mouse model, SBV-N with Saponin induced strong non-neutralizing broadly virus-reactive antibodies, decreased clinical signs, as well as significantly reduced viremia. Vaccination assays also suggest that this level of immune protection is cell mediated, as evidenced by the lack of neutralizing antibodies, as well as interferon-γ secretion observed in vitro. Therefore, based on these results, bacterially expressed SBV-N, co-administered with veterinary-grade Saponin adjuvant may serve as a promising economical alternative to current SBV vaccines, and warrant further evaluation in large ruminant animal models. Moreover, we propose that this strategy may be applicable to other bunyaviruses.
机译:Schmallenberg病毒(SBV),节肢动物传播的致病兔血清血症仍然是对欧洲畜牧业的威胁,导致年轻反刍动物牲畜中的发病率和死亡率。这里,我们描述了一种新的SBV亚基疫苗,基于施用兽医级皂苷佐剂的细菌表达的SBV核蛋白(SBV-N)。当在IFNAR - / - 小鼠模型中测定时,SBV-N具有皂苷诱导强不中和的广泛病毒反应性抗体,降低临床症状,以及显着降低的病毒血症。疫苗接种测定还表明,这种水平的免疫保护是细胞介导的,如缺乏中和抗体所证明的,以及在体外观察到的干扰素-γ分泌。因此,基于这些结果,与兽医级皂苷佐剂共同施用的细菌表达的SBV-N可用作当前SBV疫苗的有希望的经济替代品,并在大型反刍动物模型中进行进一步评估。此外,我们建议这种策略可能适用于其他兔酵母。

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