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Establishment of an Enzyme-Linked Immunosorbent Assay for Detection of Hantavirus Antibody of Rats Using a Recombinant of Nucleocapsid Protein Expressed in Escherichia coli

机译:使用在大肠杆菌中表达的核衣壳蛋白重组体检测大鼠汉坦病毒抗体的酶联免疫吸附测定方法的建立

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A recombinant nucleocapsid protein of Hantaan virus (HTN) 76-118 strain expressed in E. coli was applied as a serodiagnostic antigen in an enzyme-linked immunosorbent assay (rHTN-ELISA) for detection of hantavirus antibody in rat sera. The sensitivity and specificity of the rHTN-ELISA were compared with those of the indirect immunofluoresent assay (IFA) using virus-infected cells. The sensitivity of rHTN-ELISA was similar to that of the IFA both in experimentally SR-11 infected rat and naturally infected rat sera. Sera showing a low antibody titer in IFA and suspected to be negative by other methods were also found to be negative in rHTN-ELISA. These results indicate that rHTN-ELISA is effective as a screening method for serodiagnosis of hantaviruses, because of its high sensitivity, specificity, safety and suitability for processing large number of samples.
机译:在大肠杆菌中表达的汉坦病毒(HTN)76-118菌株重组核衣壳蛋白作为血清诊断抗原应用于酶联免疫吸附测定(rHTN-ELISA)中,用于检测大鼠血清中的汉坦病毒抗体。使用病毒感染的细胞,将rHTN-ELISA的敏感性和特异性与间接免疫荧光测定(IFA)的敏感性和特异性进行了比较。在实验性感染SR-11的大鼠和自然感染的大鼠血清中,rHTN-ELISA的敏感性均与IFA相似。在rHTN-ELISA中,还发现在IFA中抗体滴度低且被其他方法怀疑为阴性的血清也为阴性。这些结果表明,由于rHTN-ELISA具有高灵敏度,特异性,安全性和适用于处理大量样品的特点,因此可作为汉坦病毒血清诊断的有效筛选方法。

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