首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Expression of recombinant parvovirus NS1 protein by a baculovirus and application to serologic testing of rodents.
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Expression of recombinant parvovirus NS1 protein by a baculovirus and application to serologic testing of rodents.

机译:杆状病毒表达重组细小病毒NS1蛋白并将其应用于啮齿动物的血清学检测。

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摘要

A recombinant baculovirus containing the NS1 gene of minute virus of mice was constructed. Optimal expression of the recombinant NS1 protein (rNS1) was achieved by infecting Trichoplusa ni High Five cells at a multiplicity of 10 and incubating them for 72 h postinfection. An enzyme-linked immunosorbent assay (ELISA) with rNS1 as the antigen was evaluated for serologic testing of laboratory rodents. The rNS1 ELISA proved to be a more sensitive method for the detection of antibodies to recently recognized rodent parvovirus species (mouse orphan parvovirus and rat orphan parvovirus) and prototypic parvovirus species (minute virus of mice, Kilham's rat virus, and H-1) than were conventional parvovirus ELISAs that use whole parvovirus virions.
机译:构建了包含小鼠微小病毒NS1基因的重组杆状病毒。重组NS1蛋白(rNS1)的最佳表达是通过以10的倍数感染Trichoplusa ni High Five细胞并在感染后孵育72小时来实现的。以rNS1为抗原的酶联免疫吸附测定(ELISA)被评估用于实验室啮齿动物的血清学检测。 rNS1 ELISA被证明是一种比最近识别的啮齿动物细小病毒种类(小鼠孤儿细小病毒和大鼠孤儿细小病毒)和原型细小病毒种类(小鼠的细小病毒,Kilham's大鼠病毒和H-1)抗体更灵敏的检测方法。是使用整个细小病毒颗粒的常规细小病毒ELISA。

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