Mousli M, Turki I, Kharmachi H, Dellagi K
Laboratoire d'Immunopathologie, Vaccinologie et Génétique Moléculaire, Institut Pasteur de Tunis, Tunis-Belvédère, Tunisia.
Dev Biol (Basel). 2008;131:483-91.
The most widely used test for rabies diagnostics is the fluorescent antibody test, which is recommended by both the World Health Organization and the World Organisation for Animal Health (OIE). This test may be used directly on a smear, and can also be used to confirm the presence of rabies antigen in cell culture or in brain tissue for diagnosis. The colorimetric enzymes are usually coupled to an antibody by chemical means using cross-linking reagents. However, such non-specific procedures lead to heterogeneous conjugates, sometimes with reduced activity and specificity. To bypass these problems, genetic engineering has provided a way to create chimeric bifunctional molecules in which the variable domains of an antibody are genetically linked to unrelated protein tracers. In this study, we describe the successful production of a bifunctional chimeric protein based on alkaline phosphatase-fused anti-rabies virus glycoprotein scFv antibody fragment. We also report the antigen binding properties and the alkaline phosphatase activity of the recombinant conjugate protein. We established its value as a novel in vitro tool for detecting the rabies virus in brain smear in a one-step procedure; it presents a similar sensitivity and specificity to that obtained using standard reagents.
狂犬病诊断中使用最广泛的检测方法是荧光抗体检测,这是世界卫生组织和世界动物卫生组织(OIE)都推荐的方法。该检测可直接用于涂片,也可用于确认细胞培养物或脑组织中狂犬病抗原的存在以进行诊断。比色酶通常通过使用交联试剂的化学方法与抗体偶联。然而,这种非特异性程序会导致异质缀合物,有时活性和特异性会降低。为了绕过这些问题,基因工程提供了一种创建嵌合双功能分子的方法,其中抗体的可变域与不相关的蛋白质示踪剂通过基因连接。在本研究中,我们描述了基于碱性磷酸酶融合的抗狂犬病病毒糖蛋白单链抗体片段成功生产双功能嵌合蛋白的过程。我们还报告了重组缀合蛋白的抗原结合特性和碱性磷酸酶活性。我们确立了其作为一种新型体外工具在一步法检测脑涂片中狂犬病病毒的价值;它呈现出与使用标准试剂获得的灵敏度和特异性相似的结果。