呼肠孤病毒Ⅲ型免疫荧光检测方法的建立及初步应用
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中国药品生物制品检定所、国家实验动物质量检测中心,北京 100050

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Establishment and Initial Application of an Immunofluorescence Assay in Detecting Mammalian Orthoreovirus 3
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National Institute for the Quality Control of Pharmaceutical and Biological Products,National Center for Quality of Laboratory Animals,Beijing 100050,China

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    摘要:

    目的 建立呼肠孤病毒Ⅲ型( Reo3) 免疫荧光( IFA) 检测方法,应用于人用动物源性生物材料及生物制品外源 Reo3 的检测。方法 滴定病毒 TCID50,筛选 Reo3 敏感细胞,依据国标 IFA 法制备抗原片,方阵法滴定免疫荧光素最佳工作浓度。并进行特异性、敏感性和稳定性试验。结果 选 取 BSC - 1 细 胞 作 为 Reo3 敏 感 细 胞,病毒感染力滴度( TCID50 ) 为 10 - 5. 8 /mL; 免疫荧光素最佳工作浓度为 1∶ 100; 与小鼠鼠痘( Ect) 病毒、小鼠肝炎( MHV)病毒均无交叉反应; 稳定性和敏感性试验显示,不同时间 IFA 检测灵敏度均为 1∶ 1280; 可检测到的病毒滴度最低为10 - 4. 1 /mL。结论 建立的 IFA 法敏感性、特异性强,稳定性好,可用于人用动物源性生物材料及生物制品 Reo3 的检测。

    Abstract:

    Objective To establish an immunofluorescence assay ( IFA) method of detecting the mammalian orthoreovirus 3 ( Reo3) in animal-derived biological materials and biological products for human use. Methods Reo3-sensitive cells were screened. The virus TCID50 was titrated and antigen slides were prepared according to GB IFA. The best working concentration of IgG-FITC was titrated and the specificity,sensitivity and stability were tested. Results BSC-1 cells were selected as Japanese encephalitis virus ( JEV) -sensitive cells. The TCID50 of the virus was 10 - 5. 8·mL - 1. The best working concentration of the IgG-FITC was 1: 100. There was no cross-reactivity with ectromelia virus and mouse hepatitis virus. The tests of sensitivity and stability showed that the detection sensitivity was 1: 1280 at different time points. The lowest detected virus titer was 10 - 4. 1·mL - 1. Conclusions The established IFA method is good in sensitivity,specificity and stability,and can be used in detecting the Reo3 in animal-derived biological materials and biological products for human use.

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王 吉,卫 礼,岳秉飞,贺争鸣.呼肠孤病毒Ⅲ型免疫荧光检测方法的建立及初步应用[J].中国比较医学杂志,2011,21(8):1~4+86.

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  • 收稿日期:2010-03-03
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  • 在线发布日期: 2025-12-05
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