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Biotechnology letters. 2025 Apr 16;47(3):42. doi: 10.1007/s10529-025-03576-6 Q32.12025

Construction and immunogenicity analysis of a recombinant baculovirus targeting the N protein of SARS-CoV-2

SARS-CoV-2 N蛋白靶向重组杆状病毒的构建及其免疫原性分析 翻译改进

Bohan Yu  1, Xiaoli Mo  1, Li Sui  1, Yujia Fang  1, Xudong Tang  1  2, Ping Qian  3  4

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作者单位

  • 1 Jiangsu Key Laboratory of Sericultural and Animal Biotechnology, School of Biotechnology, Jiangsu University of Science and Technology, Zhenjiang, 212100, China.
  • 2 Key Laboratory of Silkworm and Mulberry Genetic Improvement, Ministry of Agriculture and Rural Affairs, Sericultural Scientific Research Center, Chinese Academy of Agricultural Sciences, Zhenjiang, 212100, China.
  • 3 Jiangsu Key Laboratory of Sericultural and Animal Biotechnology, School of Biotechnology, Jiangsu University of Science and Technology, Zhenjiang, 212100, China. qianping@just.edu.cn.
  • 4 Key Laboratory of Silkworm and Mulberry Genetic Improvement, Ministry of Agriculture and Rural Affairs, Sericultural Scientific Research Center, Chinese Academy of Agricultural Sciences, Zhenjiang, 212100, China. qianping@just.edu.cn.
  • DOI: 10.1007/s10529-025-03576-6 PMID: 40237823

    摘要 中英对照阅读

    Objectives: This study aimed to construct recombinant baculoviruses capable of expressing the nucleocapsid N protein of SARS-CoV-2 and to assess the effects of co-administration with sodium butyrate on its expression and immunogenicity. Results: The recombinant BmNPV expressed green fluorescent protein in BmN cells and N protein in mammalian... ...点击完成人机验证后继续浏览

    目标: 本研究旨在构建能够表达SARS-CoV-2核衣壳N蛋白的重组杆状病毒,并评估与丁酸钠共给药对其表达和免疫原性的影响。

    结果: 重组BmNPV在BmN细胞中表达了绿色荧光蛋白,在哺乳动物细胞中表达了N蛋白。添加丁酸钠显著增强了HEK293T细胞中N蛋白的表达。将重组BmNPV肌肉注射到小鼠体内后,分别在第7天、第21天和第35天检测到了针对N蛋白的特异性抗体。与丁酸钠(每公斤体重1000毫克)共给药显著增强了重组病毒的免疫原性。

    结论: 表达SARS-CoV-2 N蛋白的重组BmNPV成功地在小鼠中诱导了抗-N免疫原性,为开发针对SARS-CoV-2的新亚单位疫苗提供了坚实的基础。

    关键词: 杆状病毒;COVID-19 N蛋白;免疫原性蛋白质表达;丁酸钠。

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    期刊名:Biotechnology letters

    缩写:BIOTECHNOL LETT

    ISSN:0141-5492

    e-ISSN:1573-6776

    IF/分区:2.1/Q3

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    Construction and immunogenicity analysis of a recombinant baculovirus targeting the N protein of SARS-CoV-2