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首页> 外文期刊>Frontiers in Chemistry >Expression and Immunogenicity of M2e Peptide of Avian Influenza Virus H5N1 Fused to Ricin Toxin B Chain Produced in Duckweed Plants
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Expression and Immunogenicity of M2e Peptide of Avian Influenza Virus H5N1 Fused to Ricin Toxin B Chain Produced in Duckweed Plants

机译:浮萍植物产生的蓖麻毒素B链融合的禽流感病毒H5N1 M2e肽的表达及免疫原性

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摘要

The amino acid sequence of the extracellular domain of the virus-encoded M2 matrix protein (peptide M2e) is conserved among all subtypes of influenza A strains, enabling the development of a broad-range vaccine against them. We expressed M2e from avian influenza virus A/chicken/Kurgan/5/2005 (H5N1) in nuclear-transformed duckweed plants for further development of an avian influenza vaccine. The 30-amino acid N-terminal fragment of M2, including M2e (denoted M130), was selected for expression. The M2e DNA sequence fused in-frame to the 3’ end of ricin toxin B chain (RTB) was cloned under control of the CaMV 35S promoter into pBI121. The resulting plasmid was used for duckweed transformation, and 23 independent transgenic duckweed lines were obtained. Asialofetuin-binding ELISA of protein samples from the transgenic plants using polyclonal anti-RTB antibodies confirmed the expression of the RTB–M130 fusion protein in 20 lines. Quantitative ELISA of crude protein extracts from these lines showed RTB–M130 accumulation ranging from 0.25–2.5 μg/g fresh weight (0.0006–0.01% of total soluble protein). Affinity chromatography with immobilized asialofetuin and western blot analysis of protein samples from the transgenic plants showed expression of fusion protein RTB–M130 in the dimeric form with a molecular mass of about 70 kDa. Mice were immunized orally with a preparation of total soluble protein from transgenic plants, receiving four doses of 7 μg duckweed-derived RTB–M130 each, with no additional adjuvant. Specific IgG against M2e was detected in immunized mice, and the endpoint titer of anti-M2e IgG was 1024. It was confirmed that oral immunization with RTB-M2e induces production of specific antibodies against peptide M2e, one of the most conserved antigens of the influenza virus. These results may provide further information for the development of a duckweed-based expression system to produce a broad-range edible vaccine against avian influenza.
机译:病毒编码的M2基质蛋白(肽M2e)的细胞外结构域的氨基酸序列在A型流感病毒株的所有亚型中均保守,从而能够开发出针对它们的广泛疫苗。我们在核转化的浮萍植物中表达了来自禽流感病毒A / chicken / Kurgan / 5/2005(H5N1)的M2e,以进一步开发禽流感疫苗。选择M2的30个氨基酸的N末端片段,包括M2e(表示为M130)进行表达。在CaMV 35S启动子的控制下,将符合读框融合到蓖麻毒蛋白毒素B链(RTB)3'端的M2e DNA序列克隆到pBI121中。所得质粒用于浮萍转化,并获得23个独立的转基因浮萍品系。使用多克隆抗RTB抗体的转基因植物蛋白质样品的去唾液酸调节蛋白结合ELISA证实了RTB-M130融合蛋白在20个品系中的表达。这些品系中粗蛋白提取物的定量ELISA显示,RTB-M130的积累量为鲜重0.25-2.5μg/ g(占总可溶性蛋白的0.0006-0.01%)。固定化去唾液酸铁蛋白的亲和层析和转基因植物蛋白质样品的蛋白质印迹分析表明,融合蛋白RTB-M130以二聚体形式表达,分子量约为70 kDa。用转基因植物的总可溶性蛋白制剂对小鼠进行口服免疫,每只接受四剂7μg浮萍来源的RTB-M130,无其他佐剂。在免疫的小鼠中检测到针对M2e的特异性IgG,抗M2e IgG的终点滴度为1024。已证实,用RTB-M2e口服免疫可诱导产生针对肽M2e的特异性抗体,M2e是流感最保守的抗原之一。病毒。这些结果可能为开发基于浮萍的表达系统以生产抗禽流感的广泛可食用疫苗提供更多信息。

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