传染性造血器官坏死病病毒参考蛋白的研制
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北京出入境检验检疫局检验检疫技术中心,北京出入境检验检疫局检验检疫技术中心,中国检验检疫科学研究院,北京出入境检验检疫局检验检疫技术中心,北京出入境检验检疫局检验检疫技术中心,中国检验检疫科学研究院,北京出入境检验检疫局检验检疫技术中心

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质检公益性项目(201310221)


Preparation of reference protein for infectious hematopoietic necrosis virus (IHNV)
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Inspection and Quarantine Technical Center of Beijing Enter-exit Inspection and Quarantine BureauChinese Academy of Inspection and Quarantine,Inspection and Quarantine Technical Center of Beijing Enter-exit Inspection and Quarantine BureauChinese Academy of Inspection and Quarantine,,Inspection and Quarantine Technical Center of Beijing Enter-exit Inspection and Quarantine BureauChinese Academy of Inspection and Quarantine,Inspection and Quarantine Technical Center of Beijing Enter-exit Inspection and Quarantine BureauChinese Academy of Inspection and Quarantine,,Inspection and Quarantine Technical Center of Beijing Enter-exit Inspection and Quarantine BureauChinese Academy of Inspection and Quarantine

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    摘要:

    为规避活病毒作参考物质存在的生物安全风险,本研究利用毕赤酵母表达系统表达了传染性造血器官坏死病病毒(IHNV)的糖蛋白来制备参考蛋白,作为IHNV免疫学检测参考物质。本研究选用IHNV糖蛋白基因(IHNV-G)为目的基因,根据GenBank中IHNV全基因序列设计特异性引物,以IHNV-uk株病毒核酸为模板,通过RT-PCR获得糖蛋白基因片段, 将其克隆至真核表达载体pPICZαA, 转入毕赤酵母感受态细胞GS115中,使外源基因与酵母基因融合,通过1%甲醇诱导表达外源蛋白,SDS-PAGE分析显示获得可溶性表达蛋白,分子量大于70 ku。经Western Blot和ELISA分析,该表达产物可以被IHNV多抗特异性识别。0.1531 mg的重组蛋白与0.3125TCID50 IHNV在ELISA实验中反应原性相当,-20 ℃可稳定保存2个月,说明其在一定程度上可替代病毒作为参考物质。该研究为IHNV ELISA检测试剂盒的开发奠定基础。

    Abstract:

    To avoid the biosecurity risk of live virus used as a reference material, the glycoprotein gene of infectious hematopoietic necrosis virus (IHNV) was expressed in Pichia expression system to prepare reference protein,then it can be used as reference material in immunological assay. The IHNV-uk glycoprotein gene (IHNVG) was amplified by RT-PCR with the specific primers designed according to the GenBank IHNV gene sequence,then the IHNV-G was cloned to pPICZαA and transformed into GS115 to make gene fusion system of the target gene and yeast. The fusion gene was induced by 1% methanol to get soluble glycoprotein, the molecular weight of protein is than 70ku in SDS-PAGE analysis.and reactinogenicity of expressed protein was determined with goat polyclonal antibodies against IHNV by Western Blot analysis. The reactinogenicity of 0.1531 mg expressed protein was comparable to 0.3125TCID50 IHNV in ELISA analysis, and the expressed protein can exist stably for two months at -20 ℃. So it was proved that the expressed protein can replace IHNV as reference material. The study provides a foundation for the development of virus ELISA test kit.

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王树云,高志强,张旻,谷强,任彤,刘艳华,江育林,张利峰.传染性造血器官坏死病病毒参考蛋白的研制[J].水产学报,2016,40(3):388~395

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  • 收稿日期:2015-11-02
  • 最后修改日期:2015-12-09
  • 录用日期:2016-03-22
  • 在线发布日期: 2016-03-29
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