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首页|期刊导航|中国兽医科学|小鼠细小病毒单克隆抗体的制备及双抗体夹心ELISA检测方法的建立

小鼠细小病毒单克隆抗体的制备及双抗体夹心ELISA检测方法的建立

陈莉 张旭亮 刘彪 吴伟 马畅 赵迎峰

中国兽医科学2026,Vol.56Issue(3):326-334,9.
中国兽医科学2026,Vol.56Issue(3):326-334,9.DOI:10.16656/j.issn.1673-4696.2026.0037

小鼠细小病毒单克隆抗体的制备及双抗体夹心ELISA检测方法的建立

Preparation of monoclonal antibodies against minute virus of mice and establishment of a double-antibody sandwich ELISA detection method

陈莉 1张旭亮 1刘彪 1吴伟 1马畅 2赵迎峰3

作者信息

  • 1. 中国人民解放军东部战区总医院 医疗保障中心 实验动物室,江苏南京 210002
  • 2. 中国人民解放军东部战区总医院 医疗保障中心 实验动物室,江苏南京 210002||南京农业大学 农业农村部动物生理生化重点实验室,江苏南京 210095
  • 3. 中国人民解放军东部战区总医院 第三派驻门诊部,江苏南京 210002
  • 折叠

摘要

Abstract

To prepare monoclonal antibodies(McAbs)against minute virus of mice(MVM)VP2 protein and establish an MVM antigen detection method based on double-antibody sandwich ELISA,the prokaryotic expression system was employed to express the VP2 protein.The purified protein was used to immunize female BALB/c mice for the preparation of McAbs.Using the obtained McAb 1C5 as the capture antibody and HRP-labeled McAb 8B9 as the detection antibody,conditions were optimized to establish a double-antibody sandwich ELISA detection method.The sensitivity,specificity,and repeatability of the method were systematically evaluated,and a comparative analysis was conducted with qPCR detection.The MVM VP2 protein was expressed and purified,and female BALB/c mice were immunized.Following the immunization protocol,two McAbs were screened and obtained,designated as 1C5 and 8B9.Western-blot and immunofluo-rescence assays confirmed that both antibodies specifically bound to MVM virus and recombinant protein.Using these two prepared antibodies,a double-antibody sandwich ELISA method was established with 1C5 as the capture antibody and HRP-labeled 8B9 as the detection antibody.The method demonstrated a minimum detection limit of 1034 TCID50/mL for MVM virus and 50 ng/mL for recombinant protein.It showed no cross-reactivity with four common murine viruses,exhibited an inter-assay coefficient of variation below 10%,and achieved 100% overall concordance when compared with qPCR detection results.Two MVM McAbs were successfully prepared.The MVM double-antibody sandwich ELISA method established using these anti-bodies demonstrates favorable sensitivity and specificity,showing good concordance with qPCR detection.This study provides an effective detection approach for clinical diagnosis and high-throughput screening and monitoring of laboratory mice,thereby ensuring the SPF status of laboratory animals and providing healthy and reliable laboratory animals for life science research.

关键词

小鼠细小病毒/单克隆抗体/双抗体夹心ELISA/抗原检测

Key words

minute virus of mice/monoclonal antibody/double-antibody sandwich ELISA/antigen detection

分类

农业科技

引用本文复制引用

陈莉,张旭亮,刘彪,吴伟,马畅,赵迎峰..小鼠细小病毒单克隆抗体的制备及双抗体夹心ELISA检测方法的建立[J].中国兽医科学,2026,56(3):326-334,9.

基金项目

2023年科技创新项目(2023JCYJZD077,2023JCYJYB127,22JCYYYB16) (2023JCYJZD077,2023JCYJYB127,22JCYYYB16)

实验动物专项课题(SYDW-2018-11,SYDW_KY(2021)10) (SYDW-2018-11,SYDW_KY(2021)

中国兽医科学

1673-4696

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