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1.
J Immunol Methods ; 494: 113045, 2021 07.
Article in English | MEDLINE | ID: mdl-33781786

ABSTRACT

The objectives of this study are to develop and optimize indirect ELISA based on three coating antigens of porcine epidemic diarrhea virus (PEDV), recombinant spike (S12), nucleocapsid (N), and whole viral (WV) proteins, for the detection of IgG and IgA antibodies in colostrum and milk and to evaluate the diagnostic sensitivity (DSe) and diagnostic specificity (DSp) of the assay as a diagnostic method. Colostrum (n = 347) and milk (n = 272) samples from sows were employed in this assay. Indirect ELISA based on three coating antigens was assessed by receiver operating characteristic (ROC) curve analysis with a virus neutralization (VN) test as a reference method, and the cutoff value for calculating DSe and DSp was determined. S12-ELISA showed higher DSe and DSp of IgG and IgA detection compared to N- and WV-ELISA in both colostrum and milk samples. Moreover, S12-ELISA showed perfect agreement and a high correlation with the VN test, which was better than the N- and WV-ELISA for both IgG and IgA detection in colostrum and milk. In contrast, N-ELISA showed lower DSe and DSp compared to S12- and WV-ELISA, along with a correlation with VN and substantial agreement with the VN test. Nevertheless, our developed ELISAs have accuracy for repeatability in both inter- and intra-assay variation. Overall, this research demonstrates that S12-ELISA is more suitable than WV- and N-ELISA to detect IgG and IgA antibodies against PEDV from both colostrum and milk samples.


Subject(s)
Colostrum/metabolism , Coronavirus Infections/diagnosis , Enzyme-Linked Immunosorbent Assay/methods , Milk/metabolism , Porcine epidemic diarrhea virus/physiology , Swine/immunology , Animals , Antibodies, Neutralizing/metabolism , Antibodies, Viral/metabolism , Coronavirus Infections/immunology , Enzyme Assays , Female , Immunoglobulin A/metabolism , Immunoglobulin G/metabolism , Male , Observer Variation , Reproducibility of Results , Swine/virology
2.
Planta Med ; 83(18): 1412-1419, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28575911

ABSTRACT

Porcine epidemic diarrhea virus (PEDV) causes acute diarrhea, vomiting, dehydration, weight loss, and high mortality rate in neonatal piglets. Porcine epidemic diarrhea (PED) has been reported in Europe, America, and Asia including Thailand. The disease causes substantial losses to the swine industry in many countries. Presently, there is no effective PEDV vaccine available. In this study, we developed a plant-produced monoclonal antibody (mAb) 2C10 as a prophylactic candidate to prevent the PEDV infection. Recently, plant expression systems have gained interest as an alternative for the production of antibodies because of many advantages, such as low production cost, lack of human and animal pathogen, large scalability, etc. The 2C10 mAb was transiently expressed in Nicotiana benthamiana and lettuce using geminiviral vector. After purification by protein A affinity chromatography, the antibody was tested for the binding and neutralizing activity against PEDV. Our result showed that the plant produced 2C10 mAb can bind to the virus and also inhibit PEDV infection in vitro. These results show excellent potential for a plant-expressed 2C10 as a PEDV prophylaxis and a diagnostic for PEDV infection.


Subject(s)
Antibodies, Monoclonal/immunology , Coronavirus Infections/veterinary , Lactuca/immunology , Nicotiana/immunology , Porcine epidemic diarrhea virus/immunology , Swine Diseases/prevention & control , Amino Acid Sequence , Animals , Antibodies, Monoclonal/genetics , Chlorocebus aethiops , Coronavirus Infections/immunology , Coronavirus Infections/prevention & control , Coronavirus Infections/virology , Lactuca/genetics , Lactuca/virology , Molecular Farming , Neutralization Tests/veterinary , Plant Leaves/genetics , Plant Leaves/immunology , Plant Leaves/virology , Plantibodies/genetics , Plantibodies/immunology , Porcine epidemic diarrhea virus/genetics , Swine , Swine Diseases/immunology , Swine Diseases/virology , Nicotiana/genetics , Nicotiana/virology , Vero Cells
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