Wansheng Li,Yanwei Li,Minhua Li,Hongliang Zhang,Zixuan Feng,Hu Xu,Chao Li,Zhenyang Guo,Bangjun Gong,Jinmei Peng,Guohui Zhou,Zhijun Tian,Qian Wang

Int J Biol Macromol.2024 Apr 26:131842.doi: 10.1016/j.ijbiomac.2024.131842. Online ahead of print.

Abstract

Porcine reproductive and respiratory syndrome (PRRS) is one of the most widespread illnesses in the world's swine business. To detect the antibodies against PRRSV-2, a blocking enzyme-linked immunosorbent assay (B-ELISA) was developed, utilizing a PRRSV-2 N protein monoclonal antibody as the detection antibody. A checkerboard titration test was used to determine the optimal detection antibody dilution, tested pig serum dilution and purified PRRSV coated antigen concentration. After analyzing 174 negative pig sera and 451 positive pig sera, a cutoff value of 40 % was selected to distinguish between positive and negative sera using receiver operating characteristic curve analysis. The specificity and sensitivity of the assay were evaluated to equal 99.8 % and 96 %, respectively. The method had no cross-reaction with PCV2, PRV, PPV, CSFV, PEDV, TGEV, and PRRSV-1 serum antibodies, and the coefficients of variation of intra-batch and inter-batch repeatability experiments were both <10 %. A total of 215 clinical serum samples were tested, and the relative coincidence rate with commercial ELISA kit was 99.06 %, and the kappa value was 0.989, indicating that these two detection results exhibited high consistency. Overall, the B-ELISA should serve as an ideal method for large-scale serological investigation of PRRSV-2 antibodies in domestic pigs.

Keywords: Blocking ELISA; N protein monoclonal antibody; Porcine reproductive and respiratory syndrome virus-2.