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猪伪狂犬病毒gB蛋白间接化学发光抗体检测方法的建立

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研究旨在建立一种快速检测猪伪狂犬病毒(Pseudorabies virus,PRV)gB蛋白间接CLIA抗体检测方法,以期为猪伪狂犬病(Pseudorabies,PR)的防控和规模化猪群疫苗免疫水平评估提供技术支持。本研究将羧基磁珠与重组gB蛋白进行偶联反应形成免疫磁珠,利用全自动化学发光仪对各项反应条件进行优化;选用6种不同浓度的标准品绘制标准曲线;通过绘制ROC曲线确定阴阳性判定标准;初步完成方法建立后分别对其特异性、敏感度、重复性、符合率进行评估。结果显示磁珠偶联最佳pH 6。0,蛋白偶联最佳浓度为40μg/mL,10%BSA为最优封闭剂,酶标抗体最佳稀释度为1:20000,血清反应时间为5 min,酶标抗体反应时间为10 min,预激发液反应时间为5 min,最终绘制出一条R2=0。9987的标准曲线,同时将判定标准定为:≥16。78 U为阳性,<16。78 U则为阴性。方法学评估中与7种猪类病原的阳性血清均无交叉反应,敏感度略高于商业化试剂盒,批内批间系数均小于10%,与商业化ELISA试剂盒比对总符合率为98。9%。本研究建立的猪伪狂犬病毒gB蛋白间接化学发光抗体检测方法可用于PR流行病学调查及疫苗免疫水平评估,为后续试剂盒研发提供理论参考。
Establishment of an Indirect Chemiluminescent Antibody Detection Method for Porcine Pseudorabies Virus gB Protein
The aim of this study is to establish a rapid indirect CLIA antibody detection method for porcine pseudorabies virus gB protein,in order to provide technical support for the prevention and control of porcine pseudorabies disease and the evaluation of vaccine immunization level in large-scale pig herds. In this study,carboxylated magnetic beads were coupled with recombinant gB protein to form immunomagnetic beads,and the reaction conditions were optimized by using a fully automated chemiluminescence instrument;six different concentrations of standards were used to draw the standard curves;the negative and positive determination criteria were determined by drawing ROC curves;and the specificity,sensitivity,reproducibility,and compliance were evaluated after the preliminary establishment of the method. The results showed that the optimal pH for magnetic bead coupling was 6.0,the optimal concentration for protein coupling was 40μg/mL,10%BSA was the optimal sealant,the optimal dilution of enzyme-labeled secondary antibody was 1:20000,the serum reaction time was 5 min,the enzyme-labeled antibody reaction time was 10 min,and the pre-stimulation solution reaction time was 5 min. Finally,a standard curve with R2=0.9987 was drawn,and at the same time the judgment criteria were set as follows:≥16.78 U was judged as positive,and<16.78 U was judged as negative. In the methodological evaluation,there was no cross-reactivity with the positive sera of 7 porcine pathogens,and the sensitivity was slightly higher than that of the commercial kits,with intra-batch and inter-batch coefficients of less than 10%,and the total compliance rate with the commercial ELISA kits was 98.9%. The indirect chemiluminescent antibody detection method for porcine pseudorabies virus gB protein established in this study can be used for epidemiological investigation of PR and assessment of vaccine immunization level,and provides theoretical reference for the development of subsequent kits.

porcine pseudorabies virusrecombinant gB proteinchemiluminescenceantibodyimmunoassaystandard curveROC curve

向国庆、宋帅、温肖会、吕殿红、陈玉婷、连聪、贾春玲、顾有方、罗胜军

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广东省农业科学院动物卫生研究所/广东省畜禽疫病防治研究重点实验室/农业农村部兽用药物与诊断技术广东科学观测实验站,广州510640

安徽科技学院动物科学学院/动物营养调控与健康安徽省重点实验室,安徽凤阳233100

猪伪狂犬病毒 重组gB蛋白 化学发光 抗体 免疫分析 标准曲线 ROC曲线

2024

中国农学通报
中国农学会

中国农学通报

CSTPCD
影响因子:0.891
ISSN:1000-6850
年,卷(期):2024.40(36)