Development of an indirect ELISA for the immunoprotection evaluation of E2 antibodies against classical swine fever virus

The Chinese government's reclassification of Classical Swine Fever (CSF) from a class Ⅰ to a class Ⅱ animal infectious disease, now also including CSF under the disease eradication program, reflects the significant progress made through extensive immunization with CSF vaccines. In light of this...

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Veröffentlicht in:Journal of virological methods 2024-09, Vol.329, p.114999, Article 114999
Hauptverfasser: Fang, Qi, Luo, Ye, Liang, Tongtong, Liao, Rongli, Yu, Xiaohang, Zheng, Jin, Yin, Deming, Yu, Xinglong
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Sprache:eng
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Zusammenfassung:The Chinese government's reclassification of Classical Swine Fever (CSF) from a class Ⅰ to a class Ⅱ animal infectious disease, now also including CSF under the disease eradication program, reflects the significant progress made through extensive immunization with CSF vaccines. In light of this advancement, there is an imperative need for an expedient and accurate method to assess the levels of immunoprotection against classical swine fever virus (CSFV) in vaccinated pigs, a critical component in the campaign to eradicate the disease. This study develops an indirect enzyme-linked immunosorbent assay (iELISA) based on a highly glycosylated E2 protein stable expressed in CHO-K1 mammalian cells. Statistical analysis revealed strong positive correlations between the iELISA and VNT results (r = 0.9063, p < 0.0001) that were much greater than those between the IDEXX ELISA and VNT results (r = 0.8126, p < 0.0001). Taking the VNT data as the standard, the consistency of the iELISA (κ =0.880) was greater than that of the IDEXX ELISA (κ =0.699). In summary, the iELISA provides a more efficient and precise method for assessing CSFV immunity in pigs. Its reliable detection of immunoprotection levels against CSFV makes it an essential tool for optimizing CSF vaccination strategies. Consequently, its application can significantly support the ongoing efforts to eradicate CSF. •Established CHO-K1-E2 cell line stably expressing glycosylated CSFV E2 protein.•Developed indirect ELISA for the detection of CSFV E2 antibodies.•Indirect ELISA demonstrates a strong correlation with VNT.
ISSN:0166-0934
1879-0984
1879-0984
DOI:10.1016/j.jviromet.2024.114999