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基于重组核衣壳蛋白的酶联免疫吸附测定法用于检测猪流行性腹泻病毒(PEDV)抗体的开发与评估

Development and evaluation of enzyme-linked immunosorbent assay based on recombinant nucleocapsid protein for detection of porcine epidemic diarrhea (PEDV) antibodies.

作者信息

Hou Xi-Lin, Yu Li-Yun, Liu Jianzhu

机构信息

College of Animal Science and Technology, Heilongjiang August First Land Reclamation University, Daqin 163319, China.

出版信息

Vet Microbiol. 2007 Jul 20;123(1-3):86-92. doi: 10.1016/j.vetmic.2007.02.014. Epub 2007 Feb 20.

Abstract

An enzyme-linked immunosorbent assays (ELISA) based on recombinant nucleocapsid (N) protein generated in Escherichia coli was evaluated for its sensitivity and specificity for diagnosis of porcine epidemic diarrhea (PEDV) infection. The N gene encoding the N protein was cloned and expressed as a fusion protein with His tag protein in E. coli. The recombinant N protein was migrated at 48 kDa and reacted with six histidine tag specific monoclonal antibody by immunoblotting. Recombinant N protein ELISA (rnELISA) demonstrated 98.7% specificities among (80) PEDV-free individuals, and 98% sensitivity ranging among (103) clinical samples with PEDV. On testing 884 field samples, an overall agreement of 88.3% was generated between the SN and rnELISA. Taken together, these results indicated that nucleocapsid protein may be a useful antigen for the sera-diagnosis of PEDV and it was also suggested that the ELISA is a highly sensitive and specific test for detecting antibodies to PEDV.

摘要

评估了一种基于在大肠杆菌中产生的重组核衣壳(N)蛋白的酶联免疫吸附测定(ELISA)对猪流行性腹泻病毒(PEDV)感染诊断的敏感性和特异性。编码N蛋白的N基因被克隆,并在大肠杆菌中作为与His标签蛋白的融合蛋白表达。重组N蛋白在48 kDa处迁移,并通过免疫印迹与六种组氨酸标签特异性单克隆抗体反应。重组N蛋白ELISA(rnELISA)在80头无PEDV的个体中显示出98.7%的特异性,在103份PEDV临床样本中显示出98%的敏感性。在检测884份现场样本时,SN和rnELISA之间的总体一致性为88.3%。综上所述,这些结果表明核衣壳蛋白可能是PEDV血清诊断的有用抗原,并且还表明ELISA是检测PEDV抗体的高度敏感和特异的检测方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1556/7117327/1d8119ac919e/gr1.jpg

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