AI Article Synopsis

  • Pseudorabies (PR) is a viral disease primarily affecting pigs, causing significant economic losses in farming, especially due to new viral variants emerging in China.
  • To combat this, researchers developed monoclonal antibodies by immunizing mice, leading to a highly specific immunochromatography test strip for detecting PRV infections in pigs.
  • This test strip outperformed other methods with a 96.4% agreement with RT-PCR and showed high sensitivity, making it a valuable tool for monitoring PRV outbreaks and ensuring vaccine quality.

Article Abstract

Introduction: Pseudorabies (PR) is a multi-animal comorbid disease caused by pseudorabies virus (PRV), which are naturally found in pigs. At the end of 2011, the emergence of PRV variant strains in many provinces in China had caused huge economic losses to pig farms. Rapid detection diagnosis of pigs infected with the PRV variant helps prevent outbreaks of PR. The immunochromatography test strip with colloidal gold nanoparticles is often used in clinical testing due to its low cost and high throughput.

Methods: This study was designed to produce monoclonal antibodies targeting PRV through immunization of mice using the eukaryotic system to express the gE glycoprotein. Subsequently, paired monoclonal antibodies were screened based on their sensitivity and specificity for use in the preparation of test strips.

Results And Discussion: The strip prepared in this study was highly specific, only PRV was detected, and there was no cross-reactivity with glycoprotein gB, glycoprotein gC, glycoprotein gD, and glycoprotein gE of herpes simplex virus and varicellazoster virus, porcine epidemic diarrhea virus, Senecavirus A, classical swine fever virus, porcine reproductive and respiratory syndrome virus, and porcine parvovirus. Moreover, it demonstrated high sensitivity with a detection limit of 1.336 × 10 copies/μL (the number of viral genome copies per microliter); the coincidence rate with the RT-PCR detection method was 96.4%. The strip developed by our laboratory provides an effective method for monitoring PRV infection and controlling of PR vaccine quality.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11099248PMC
http://dx.doi.org/10.3389/fmicb.2024.1399123DOI Listing

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