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Updated: May 2, 2026

Optimization of a Quantitative Micro-neutralization Assay
Published on: December 14, 2016
Comparison of JEV neutralization assay using pseudotyped JEV with the conventional plaque-reduction neutralization
Hee-Jung Lee1, Kyung-Il Min, Ki Hoon Park
1Department of Bio-industrial technologies, Konkuk University, Seoul, 143-701, Republic of Korea.
A new pseudotyped-Japanese Encephalitis Virus (JEV-PV) assay offers a simpler, safer, and faster method for measuring JEV neutralizing antibodies (NAb). This JEV-PV assay closely correlates with the standard plaque-reduction neutralization test (PRNT).
Area of Science:
- Virology
- Immunology
- Assay Development
Background:
- Japanese Encephalitis Virus (JEV) poses a significant public health threat.
- Accurate measurement of JEV neutralizing antibodies (NAb) is crucial for vaccine efficacy assessment.
- The plaque-reduction neutralization test (PRNT) is the current standard but has limitations.
Purpose of the Study:
- To evaluate a novel pseudotyped-JEV (JEV-PV) assay system for measuring JEV NAb.
- To compare the JEV-PV assay's performance against the established PRNT.
- To determine the suitability of the JEV-PV assay as a replacement for PRNT.
Main Methods:
- Development of a JEV-PV based neutralization assay.
- Comparison of JEV-PV assay with PRNT for repeatability, reproducibility, and specificity.
- Correlation analysis of NAb titers obtained from both assay methods.
Main Results:
- The JEV-PV assay demonstrated simplicity, safety, and speed advantages over PRNT.
- Close correlation was observed between JEV-PV assay results and PRNT (50% plaque reduction method).
- All analytical acceptance criteria for validation were met.
Conclusions:
- The JEV-PV assay is a viable, safe, and simple alternative for measuring JEV NAb titers.
- This assay can serve as an effective method for assessing JEV neutralization potency.
- The JEV-PV assay shows potential as a new standard for JEV NAb evaluation.
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