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牛呼吸道合胞病毒融合蛋白基因的杆状病毒表达及重组蛋白在诊断酶免疫测定中的应用

Baculovirus expression of the fusion protein gene of bovine respiratory syncytial virus and utility of the recombinant protein in a diagnostic enzyme immunoassay.

作者信息

Pastey M K, Samal S K

机构信息

Virginia-Maryland Regional College of Veterinary Medicine, University of Maryland, College Park 20742, USA.

出版信息

J Clin Microbiol. 1998 Apr;36(4):1105-8. doi: 10.1128/JCM.36.4.1105-1108.1998.

Abstract

The fusion (F) protein of bovine respiratory syncytial virus (BRSV) was expressed by using a baculovirus vector. Antigenicity was tested by immunofluorescence analysis with F-specific monoclonal and polyclonal antibodies. Antibodies to recombinant F protein raised in a rabbit neutralized BRSV and human respiratory syncytial virus infectivity when tested in a plaque reduction assay. The recombinant F protein was evaluated as a source of antigen in an enzyme-linked immunosorbent assay (ELISA), and this ELISA was compared with the virus neutralization (VN) test for detecting BRSV antibodies in 10 consecutive serum samples from four calves vaccinated with a live modified BRSV vaccine and from two nonvaccinated control calves. The ELISA with the baculovirus-expressed F protein as an antigen compared favorably with the VN test and is a rapid, sensitive, and specific method for detecting serum antibodies to BRSV.

摘要

利用杆状病毒载体表达牛呼吸道合胞病毒(BRSV)的融合(F)蛋白。通过用F特异性单克隆抗体和多克隆抗体进行免疫荧光分析来检测抗原性。在蚀斑减少试验中检测时,兔体内产生的针对重组F蛋白的抗体中和了BRSV和人呼吸道合胞病毒的感染性。在酶联免疫吸附测定(ELISA)中评估重组F蛋白作为抗原的来源,并将该ELISA与病毒中和(VN)试验进行比较,以检测来自4头接种了减毒活BRSV疫苗的小牛和2头未接种对照小牛的10份连续血清样本中的BRSV抗体。以杆状病毒表达的F蛋白作为抗原的ELISA与VN试验相比具有优势,是一种检测BRSV血清抗体的快速、灵敏且特异的方法。

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Arch Virol. 1985;84(1-2):1-52. doi: 10.1007/BF01310552.
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Demonstration that glycoprotein G is the attachment protein of respiratory syncytial virus.
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