Abstract
Plaque reduction neutralization tests (PRNTs) are the gold standard for measuring neutralizing antibodies but are labor-intensive, low-throughput, and subject to variability from manual plaque counting. We developed a NanoLuc-based microneutralization (mNT) assay using rMP12-NanoLuc that quantifies luminescence in culture supernatants as a surrogate for infection. The assay runs in 96-well plates without overlay, fixation, or staining, using 35 focus-forming unit (FFU) per well and a 40 hour readout with back-titration to ensure accuracy. mNT titers from vaccinated animal sera showed strong correlation with conventional PRNTs. This approach enables rapid, reproducible, high-throughput detection of RVFV neutralizing antibodies, with the main limitations being substrate cost and the requirement for a luminometer.•The assay enables high-throughput, objective neutralization testing in 96-well plates.•Optimized conditions yield mNT titers that strongly correlate with conventional PRNTs.•Limitations include NanoLuc substrate cost and the need for a luminometer.
| Original language | English (US) |
|---|---|
| Article number | 103948 |
| Journal | MethodsX |
| Volume | 16 |
| DOIs | |
| State | Published - Jun 2026 |
Keywords
- Assay development
- MP-12 strain
- Microneutralization assay
- NanoLuc
- Neutralization antibody
- Rift valley fever virus
ASJC Scopus subject areas
- General
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