首页> 外文期刊>Frontiers in Microbiology >Influenza Viral Vectors Expressing Two Kinds of HA Proteins as Bivalent Vaccine Against Highly Pathogenic Avian Influenza Viruses of Clade 2.3.4.4 H5 and H7N9
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Influenza Viral Vectors Expressing Two Kinds of HA Proteins as Bivalent Vaccine Against Highly Pathogenic Avian Influenza Viruses of Clade 2.3.4.4 H5 and H7N9

机译:流感病毒载体表达两种HA蛋白作为针对进化枝2.3.4.4 H5和H7N9的高致病性禽流感病毒的二价疫苗

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The H5 and H7N9 subtypes of highly pathogenic avian influenza viruses (HPAIVs) in China pose a serious challenge to public health and the poultry industry. In this study, a replication competent recombinant influenza A virus of the í5N1 subtype expressing the H7 HA1 protein from a tri-cistronic NS segment was constructed. A heterologous dimerization domain was used to combine with the truncated NS1 protein of 73 amino acids to increase protein stability. H7 HA1, nuclear export protein coding region, and the truncated NS1 were fused in-frame into a single open reading frame via 2A self-cleaving peptides. The resulting PR8-H5-NS1(73)H7 stably expressed the H5 HA and H7 HA1 proteins, and exhibited similar growth kinetics as the parental PR8-H5 virus in vitro . PR8-H5-NS1(73)H7 induced specific hemagglutination inhibition (HI) antibody against H5, which was comparable to that of the combination vaccine of PR8-H5 and PR8-H7. The HI antibody titers against H7 virus were significantly lower than that by the combination vaccine. PR8-H5-NS1(73)H7 completely protected chickens from challenge with both H5 and H7 HPAIVs. These results suggest that PR8-H5-NS1(73)H7 is highly immunogenic and efficacious against both H5 and H7N9 HPAIVs in chickens. Highlights : - PR8-H5-NS1(73)H7 simultaneously expressed two HA proteins of different avian influenza virus subtypes. - PR8-H5-NS1(73)H7 was highly immunogenic in chickens. - PR8-H5-NS1(73)H7 provided complete protection against challenge with both H5 and H7N9 HPAIVs.
机译:中国的高致病性禽流感病毒(HPAIV)的H5和H7N9亚型对公共卫生和家禽业构成了严峻挑战。在这项研究中,构建了一个具有复制能力的重组A型流感病毒,该重组A5N1亚型表达了来自三顺反式NS片段的H7 HA1蛋白。使用异源二聚化结构域与73个氨基酸的截短的NS1蛋白结合以增加蛋白稳定性。 H7 HA1,核输出蛋白编码区和截短的NS1通过2A自裂解肽框内融合到单个开放阅读框中。所得的PR8-H5-NS1(73)H7稳定表达H5 HA和H7 HA1蛋白,并在体外表现出与亲代PR8-H5病毒相似的生长动力学。 PR8-H5-NS1(73)H7诱导了针对H5的特异性血凝抑制(HI)抗体,与PR8-H5和PR8-H7的联合疫苗相当。抗H7病毒的HI抗体效价明显低于联合疫苗。 PR8-H5-NS1(73)H7完全保护了鸡免受H5和H7 HPAIV的攻击。这些结果表明,PR8-H5-NS1(73)H7具有高度免疫原性,并且对鸡中的H5和H7N9 HPAIV均有效。要点:-PR8-H5-NS1(73)H7同时表达两种不同禽流感病毒亚型的HA蛋白。 -PR8-H5-NS1(73)H7在鸡中具有高度免疫原性。 PR8-H5-NS1(73)H7提供了针对H5和H7N9 HPAIV的全面保护。

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