De Diego M, Brocchi E, Mackay D, De Simone F
Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia, Brescia, Italy.
Arch Virol. 1997;142(10):2021-33. doi: 10.1007/s007050050219.
A diagnostic assay to differentiate antibodies induced by foot-and-mouth disease virus (FMDV) infection from those induced by vaccination was developed. The test is an indirect-trapping ELISA which uses a monoclonal antibody to trap the non-structural 3ABC-FMDV polypeptide expressed in E. coli. Experimental and field sera from naive, vaccinated and infected cattle were examined. Using the established threshold of 0.20 optical density units, the sensitivity of the assay was 100%, as all the experimental post-infection sera (n degree = 137) gave values greater than this threshold, irrespective of the FMDV serotype used for the infection. In contrast, more than 99% of sera from vaccinated animals were negative (225 out of 228 primo-vaccinates and 159 out of 159 multi-vaccinates). A high degree of specificity was also confirmed by the finding that 99.5% (442 out of 444) of sera from naive animals gave negative results. Serum conversion against 3ABC was first detected 8 days post-infection and demonstrable levels of 3ABC specific antibodies were detectable at least 1 year post-infection. The described 3ABC-ELISA is safe, cheap and also easy to perform in large scale serological surveys. The high specificity and sensitivity makes this test an ideal tool for FMD eradication campaigns and control programs.
开发了一种诊断检测方法,用于区分由口蹄疫病毒(FMDV)感染诱导产生的抗体与疫苗接种诱导产生的抗体。该检测方法是一种间接捕获ELISA,它使用单克隆抗体捕获在大肠杆菌中表达的非结构3ABC - FMDV多肽。对来自未接触过病毒、接种过疫苗和感染过病毒的牛的实验血清和现场血清进行了检测。使用设定的0.20光密度单位阈值,该检测方法的灵敏度为100%,因为所有感染后的实验血清(n = 137)的值均高于此阈值,无论用于感染的FMDV血清型如何。相比之下,接种过疫苗的动物中超过99%的血清呈阴性(初次接种的228份中有225份,多次接种的159份中有159份)。未接触过病毒的动物血清中99.5%(444份中的442份)呈阴性结果,这一发现也证实了该检测方法具有高度特异性。感染后8天首次检测到针对3ABC的血清转化,并且在感染后至少1年可检测到3ABC特异性抗体的可检测水平。所描述的3ABC - ELISA安全、廉价,并且在大规模血清学调查中也易于操作。高特异性和灵敏度使该检测方法成为口蹄疫根除运动和防控计划的理想工具。