A colloidal gold test strip assay for the detection of African swine fever virus based on two monoclonal antibodies against P30

2021 ◽  
Vol 166 (3) ◽  
pp. 871-879
Author(s):  
Xinyu Zhang ◽  
Xiaoyu Liu ◽  
Xiaodong Wu ◽  
Weijie Ren ◽  
Yanli Zou ◽  
...  
2021 ◽  
Vol 8 ◽  
Author(s):  
Xuexiang Yu ◽  
Xianjing Zhu ◽  
Xiaoyu Chen ◽  
Dongfan Li ◽  
Qian Xu ◽  
...  

African swine fever (ASF) is a highly lethal hemorrhagic viral disease of domestic pigs caused by African swine fever virus (ASFV). A sensitive and reliable serological diagnostic assay is required, so laboratories can effectively and quickly detect ASFV infection. The p30 protein is abundantly expressed early in cells and has excellent antigenicity. Therefore, this study aimed to produce and characterize p30 monoclonal antibodies with an ultimate goal of developing a monoclonal antibody-based enzyme-linked immunosorbent assay (ELISA) for ASFV antibody detection. Three monoclonal antibodies against p30 protein that were expressed in E. coli were generated, and their characterizations were investigated. Furthermore, a blocking ELISA based on a monoclonal antibody was developed. To evaluate the performance of the assay, 186 sera samples (88 negative and 98 positive samples) were analyzed and a receiver-operating characteristic (ROC) analysis was applied to determine the cutoff value. Based on the ROC analysis, the area under the curve (AUC) was 0.997 (95% confidence interval: 99.2 to 100%). Besides, a diagnostic sensitivity of 97.96% (95% confidence interval: 92.82 to 99.75%) and a specificity of 98.96% (95% confidence interval: 93.83 to 99.97%) were achieved when the cutoff value was set to 38.38%. Moreover, the coefficients of inter- and intra-batches were <10%, indicating the good repeatability of the method. The maximum dilution of positive standard serum detected by this ELISA method was 1:512. The blocking ELISA was able to detect seroconversion in two out of five pigs at 10 Dpi and the p30 response increasing trend through the time course of the study (0–20 Dpi). In conclusion, the p30 mAb-based blocking ELISA developed in this study demonstrated a high repeatability with maximized diagnostic sensitivity and specificity. The assay could be a useful tool for field surveillance and epidemiological studies in swine herd.


2019 ◽  
Vol 269 ◽  
pp. 197632 ◽  
Author(s):  
Vlad Petrovan ◽  
Fangfeng Yuan ◽  
Yanhua Li ◽  
Pengcheng Shang ◽  
Maria V. Murgia ◽  
...  

1985 ◽  
Vol 54 (1) ◽  
pp. 199-206 ◽  
Author(s):  
A Sanz ◽  
B García-Barreno ◽  
M L Nogal ◽  
E Viñuela ◽  
L Enjuanes

Talanta ◽  
2020 ◽  
Vol 219 ◽  
pp. 121284 ◽  
Author(s):  
Chengfei Li ◽  
Xinglin He ◽  
Yong Yang ◽  
Wenxiao Gong ◽  
Kun Huang ◽  
...  

Author(s):  
G. J. Letchworth III ◽  
T. C. Whyard ◽  
S. H. Wool

The primary purpose of this study was to devise a procedure in which a large number of monoclonal antibodies could be tested against several African swine fever virus (ASFV) preparations (virus, infected cells). The procedure had to be rapid, use a small sample and provide for some TEM.Monoclonal antibodies were produced by standard methods using myeloma cells and lymphocytes from mice immunized against ASF viral proteins. Antibodies were characterized by immunoprecipitation of radio-labelled viral proteins (Fig 1).The viral preparations used in this study were either infected macrophages, culture fluid supernatant from ASFV-infected macrophages or red blood cells from infected pigs. Each of the three viral preparations was tested by two indirect immune electron microscopy (IEM) methods; a grid method and a test tube method. In the grid method, formvar coated grids were floated on a viral preparation then for one hour each on the mouse monoclonal antibody and finally on ferritin tagged sheep anti-mouse IgG with washes between each step.


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