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March 10, 2026BMC Veterinary Research1 citationsOpen Access

Development of an automated chemiluminescence immunoassay for detection of IgA antibodies against porcine epidemic diarrhea virus spike

DLDuan LiDZDaoping ZengQWQi Wang

Key Points

  • This research aims to create an automated immunoassay for detecting IgA antibodies against PEDV to monitor vaccine effectiveness.
  • Developed a fully automated chemiluminescence immunoassay (CLIA) for detection of antibodies.
  • Utilized recombinant S1 protein-coated magnetic particles for antibody capture.
  • Employed acridinium ester-labeled mouse anti-pig IgA monoclonal antibody for signal generation.
  • Achieved diagnostic sensitivity of 96.30% and specificity of 98.48%.
  • Demonstrated repeatability with a coefficient of variation < 10%.
  • Showed 93.93% agreement with a commercial ELISA while having a broader dynamic range (35.48-fold).
  • Correlated well with virus neutralization titers, with R² values of 0.6660 for serum and 0.7639 for milk.

Abstract

Porcine epidemic diarrhoea virus (PEDV) causes substantial financial losses on pig farming worldwide. Monitoring PEDV-specific IgA antibodies is essential for assessing vaccine efficacy. In this study, we developed a fully automated chemiluminescence immunoassay (CLIA) for the detection of PEDV IgA antibodies in both serum and milk. This S1-CLIA utilizes recombinant S1 protein-coated magnetic particles (S1-MPs) for antibody capture and an acridinium ester-labeled mouse anti-pig IgA monoclonal antibody (mpIgA-AE) to generate chemiluminescence signals. Under optimized conditions, S1-CLIA achieved a diagnostic sensitivity of 96.30% and specificity of 98.48%, with a cut-off index of 1.0. S1-CLIA exhibited excellent repeatability (coefficient of variation < 10%) and no cross-reactivity with sera positive for other common swine pathogens. Compared to a commercial enzyme-linked immunosorbent assay (ELISA), S1-CLIA achieved 93.93% agreement rate, but offered a significantly broader dynamic range (35.48-fold). Notably, S1-CLIA results correlated well with virus neutralization titers (VNT), yielding R² values of 0.6660 (serum) and 0.7639 (milk). With capability of fully automated testing, this novel S1-CLIA presents a robust platform for large-scale evaluation of PEDV immunity.

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Cite This Study

Li et al. (2026) studied this question.

synapsesocial.com/papers/69af94c970916d39fea4bb82https://doi.org/10.1186/s12917-026-05407-w
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