Development of an indirect enzyme-linked immunosorbent assay (ELISA) to differentiate antibodies against wild-type porcine reproductive and respiratory syndrome from the vaccine strain TJM-F92 based on a recombinant Nsp2 protein
Autor: | Huai Huan Wu, Feng-Xue Wang, Yong-Jun Wen, Nong Song, Zhong Li, Xiurong Wang, Xiu-Fang Wang |
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Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Swine Enzyme-Linked Immunosorbent Assay Viral Nonstructural Proteins Antibodies Viral Sensitivity and Specificity law.invention 03 medical and health sciences Vaccine strain law Virology Animals Porcine respiratory and reproductive syndrome virus Respiratory system Antigens Viral chemistry.chemical_classification biology Wild type Viral Vaccines Recombinant Proteins Amino acid Vaccination 030104 developmental biology Enzyme chemistry biology.protein Recombinant DNA Antibody |
Zdroj: | Journal of Virological Methods. 251:151-154 |
ISSN: | 0166-0934 |
DOI: | 10.1016/j.jviromet.2017.09.001 |
Popis: | An accurate ELISA method to differentiate pigs infected with wild-type porcine reproductive and respiratory syndrome (PRRSV) strains from vaccinated ones would help to monitor PRRSV vaccination compliance. The recombinant protein GST-d120aa derived from the continuous deletion of 120 amino acids in the non-structural protein 2 region of the modified-live vaccine strain TJM-F92 was used to develop an indirect enzyme-linked immunosorbent assay (d120-ELISA) for differentiating serum antibodies against TJM-F92 from other PRRSV strains. At the optimized cut-off value which was calculated at an S/P of 0.25, it yielded a sensitivity of 90.7% and a specificity of 95.1%. Cross-reactivity tests suggested that the d120-ELISA was PRRSV-specific. Coefficient of variations of the repeatability tests ranged between 1.41-17.02%. The results suggest that the d120-ELISA is suitable for differentiating animals infected with wild-type strains from those immunized with MLV TJM-F92. |
Databáze: | OpenAIRE |
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