Differential diagnosis of PRV-infected versus vaccinated pigs using a novel EuNPs-virus antigen probe-based blocking fluorescent lateral flow immunoassay

Biosens Bioelectron. 2020 May 1:155:112101. doi: 10.1016/j.bios.2020.112101. Epub 2020 Feb 15.

Abstract

A novel time-resolved fluorescence blocking lateral flow immunoassay (TRF-BLFIA) was developed for on-site differential diagnosis of pseudorabies virus (PRV)-infected and vaccinated pigs using europium nanoparticles (EuNPs)-labeled virion antigens and high titer PRV gE monoclonal antibodies (PRV gE-mAb). Upon application of a positive serum sample, the specific epitopes of gE protein on the EuNPs-PRV probe were blocked, inhibiting binding to the PRV gE-mAb on the T line, resulting in low or negligible fluorescence signal, whereas when a negative sample was applied, EuNPs-PRV probes would be able to bind the antibody at the T line, leading to high fluorescence signal. Under optimized conditions, TRF-BLFIA provided excellent sensitivity and selectivity. When testing swine clinical samples (n = 356), there was 96.1% agreement between this method and a most widely used commercial gE-ELISA kit. Moreover, our method was rapid (15 min), cost-efficient and easy to operate with simple training, allowing for on-site detection. Thus, TRF-BLFIA could be a practical tool to differentially diagnose PRV-infected and vaccinated pigs.

Keywords: Differential diagnosis; Europium nanoparticles; Porcine serum; Time-resolved fluorescence immunoassay; Wild-type pseudorabies virus.

MeSH terms

  • Animals
  • Antibodies, Viral / blood
  • Antibodies, Viral / immunology
  • Antigens, Viral* / immunology
  • Europium*
  • Fluorescent Antibody Technique*
  • Herpesvirus 1, Suid / immunology*
  • Metal Nanoparticles*
  • Pseudorabies / diagnosis*
  • Pseudorabies / immunology
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Swine
  • Swine Diseases / diagnosis*
  • Swine Diseases / immunology

Substances

  • Antibodies, Viral
  • Antigens, Viral
  • Europium