Ure Agustín E, Ghiringhelli P Daniel, Possee Robert D, Morikawa Shigeru, Romanowski Víctor
Facultad de Ciencias Exactas, Instituto de Biotecnología y Biología Molecular, Universidad Nacional de La Plata, Consejo Nacional de Investigaciones Científicas y Técnicas, La Plata, Argentina.
J Med Virol. 2008 Dec;80(12):2127-33. doi: 10.1002/jmv.21265.
Junín arenavirus is the etiologic agent of Argentine hemorrhagic fever. Due to its morbidity and high mortality rate in untreated cases, this endemic disease is of mandatory report in Argentina. Secure and accurate diagnostic methods are needed for the epidemiological surveillance of the disease. Current assays rely on antigens prepared from lysates of virus infected mammalian cells. The bio-safety issue related to the manipulation of large quantities of virus restricts such antigen production to laboratories with the appropriate containment facilities. In this report, we describe the development of an enzyme linked immunosorbent assay for the etiologic confirmation of the disease, based on recombinant antigens expressed in insect cells. Eight different variables of the assay were optimized with the Taguchi approach for experimental design (L18 design, seven three-level factors and one two-level factor). The area under the receiver operating characteristics (ROC) curve was 0.966, showing the high accuracy of the test discriminating positive from negative samples. Taking into account the biosafety benefits, the high yields of antigen in cell culture, and the general performance of the assay, it is expected that it will be a useful alternative to the current ELISA for the detection of antibodies in sera from convalescent patients.
胡宁沙粒病毒是阿根廷出血热的病原体。由于其在未治疗病例中的发病率和高死亡率,这种地方病在阿根廷属于法定报告疾病。对该疾病进行流行病学监测需要安全准确的诊断方法。目前的检测方法依赖于从病毒感染的哺乳动物细胞裂解物中制备的抗原。与大量病毒操作相关的生物安全问题将此类抗原的生产限制在具备适当防护设施的实验室。在本报告中,我们描述了一种基于昆虫细胞中表达的重组抗原的酶联免疫吸附测定法,用于该疾病的病原学确认。采用田口方法对实验设计的八个不同变量进行了优化(L18设计,七个三级因素和一个二级因素)。受试者工作特征(ROC)曲线下面积为0.966,表明该检测方法在区分阳性和阴性样本方面具有很高的准确性。考虑到生物安全优势、细胞培养中抗原的高产量以及该检测方法的总体性能,预计它将成为目前用于检测康复患者血清中抗体的ELISA的有用替代方法。