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May 8, 2026Poultry science and management.0 citationsOpen Access

A rapid and sensitive lanthanide-based fluorescent microsphere immunochromatographic test for semi-quantitative detection of infectious bursal disease virus in poultry

YWYuxin WuZZZekai ZhangHZHaiqi Zhao

Key Points

  • This study aims to develop a rapid and sensitive test for semi-quantitative detection of IBDV antigen in poultry.
  • Constructed a fluorescent microsphere immunochromatographic test strip using lanthanide microspheres.
  • Optimized reaction conditions and established a quantitative standard curve with inactivated IBDV.
  • Evaluated test performance with 50 clinical samples against the national standard RT-PCR method.
  • The assay achieved 95% concordance with RT-PCR, identifying various IBDV strains accurately.
  • Showed high sensitivity, detecting IBDV antigen at dilutions up to 1:5120.
  • Demonstrated low coefficients of variation (< 10%) for repeatability, confirming reliability.

Abstract

Infectious bursal disease virus (IBDV) is a major immunosuppressive pathogen threatening global poultry production. The emergence of very virulent (vvIBDV) and novel variant strains (nVarIBDV) has increased immune escape and reduced vaccine effectiveness, underscoring the need for rapid and reliable diagnostic tools. To promote antigen detection technologies which usually time-consuming and require specialized laboratory facilities, this study developed a simple, rapid, and sensitive fluorescent microsphere immunochromatographic test strip (FM-ICTS) for semi-quantitative detection of IBDV antigen. The FM-ICTS was constructed using lanthanide fluorescent microspheres conjugated to an anti-VP2 monoclonal antibody within a double-antibody sandwich lateral flow format. Reaction conditions were optimized, and a quantitative standard curve was established using serial dilutions of inactivated IBDV (B87 strain). The assay generated stable fluorescence signals within 15 min and showed high analytical sensitivity, detecting IBDV antigen at dilutions up to 1:5120. No cross-reactivity with Chicken Anemia Virus (CAV), Avian Leukosis Virus(ALV), Avian Influenza Virus(AIV), or Marek’s Disease Virus(MDV) was observed, confirming excellent specificity. Repeatability tests demonstrated low coefficients of variation (< 10%). When evaluated using 50 clinical samples, FM-ICTS exhibited 95% concordance with the national standard RT-PCR method and accurately identified vvIBDV, classical infectious bursal disease virus (clIBDV), and nVarIBDV strains. With significant cost advantage and capability of relative quantification, the developed FM-ICTS provides a candidate method suitable for field diagnostics and vaccine quality monitoring.

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Cite This Study

Wu et al. (2026) studied this question.

synapsesocial.com/papers/69fd7f4fbfa21ec5bbf07d74https://doi.org/10.1186/s44364-026-00026-5
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Immunochromatographic Gold-Based Test Strip for Rapid Detection of <i>Infectious Bursal Disease Virus</i> Antibodies2011 · 20 citations
  2. 2Advancing IBDV diagnostics: a one-step multiplex real-time qRT-PCR for discriminating between vvIBDV and non-vvIBDV viruses, including the newly emerged IBDV variant2024 · 1 citations
  3. 3A New Dual Fluorescence Method for Rapid Detection of Infectious Bronchitis Virus at Constant Temperature2024 · 2 citations
  4. 4Development of an In-House Indirect ELISA kit for the serological detection of antibodies against infectious bursal disease in Chickens of Ethiopia2024
  5. 5Production and diagnostic application of monoclonal antibodies against infectious bursal disease virus2011