Hou Xi-Lin, Yu Li-Yun, Liu Jianzhu
College of Animal Science and Technology, Heilongjiang August First Land Reclamation University, Daqin 163319, China.
Vet Microbiol. 2007 Jul 20;123(1-3):86-92. doi: 10.1016/j.vetmic.2007.02.014. Epub 2007 Feb 20.
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.
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。