Cross Robert W, Ksiazek Thomas G
Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
Galveston National Laboratory, University of Texas Medical Branch at Galveston, Galveston, TX, USA.
Methods Mol Biol. 2017;1628:363-372. doi: 10.1007/978-1-4939-7116-9_29.
Ebola viruses are high-priority pathogens first discovered in rural Africa associated with sporadic outbreaks of severe hemorrhagic disease in humans and nonhuman primates. Little is known about the disease ecology or the prevalence of past exposure of human populations to any of the five species of the genus Ebolavirus. The use of immunologic means of detection for either virus antigens or the host's immune response to antigen associated with prior infections offers a powerful approach at understanding the epidemiology and epizootiology of these agents. Here we describe methods for preparing antigen detection sandwich enzyme-linked immunosorbent assays (ELISAs) as well as IgG and IgM ELISAs for the detection of ebolavirus antigens or antibodies in biological samples.
埃博拉病毒是一类高优先级病原体,最早在非洲农村地区被发现,与人类和非人灵长类动物中偶发的严重出血热疫情相关。对于该疾病的生态情况以及人类群体过去接触埃博拉病毒属五种病毒中任何一种的流行程度,我们知之甚少。利用免疫检测手段来检测病毒抗原或宿主针对既往感染相关抗原的免疫反应,为了解这些病原体的流行病学和动物流行病学提供了一种强有力的方法。在此,我们描述了用于制备抗原检测夹心酶联免疫吸附测定(ELISA)以及用于检测生物样品中埃博拉病毒抗原或抗体的IgG和IgM ELISA的方法。