Method Article

Analyzing the Antigenic Relationship between Viruses using an Image-Based Microneutralization Assay

July 8th, 2025

In This Article

Abstract

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Source: Lin, Y., et al. Optimization of a Quantitative Micro-neutralization Assay. J. Vis. Exp. (2016)

This video demonstrates the imaging-based micro-neutralization assay to analyze the antigenic relations between influenza A and B viruses. It provides a quantitative and visual way to assess the effectiveness of antibodies or other treatments in preventing viral infection.

Protocol

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1. Virus Titration

NOTE: Depending on the number of viruses and the number of duplicates, a well plate can be set up with the following flexibilities: (1) The viral dilution can be arranged along either the rows or the columns (Figure 1). Each virus should occupy a separate row/column. (2) The viral dilution increment is flexible, but it should start with the highest viral concentration at the top-left corner. (3) There is no restriction on the number of duplicates.

  1. Aliquot sufficient MDCK cells or MDCK-SIAT cells8 into 96-well plates (200 µl/well). Incubate the cells at 37....

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Results

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Viral dilution plate diagram, serial dilution process, virus titration analysis, microtiter setup.
Figure 1: Example of a well-plate setup in a virus titration experiment. Test viruses are assigned to separate rows (A to H). Columns are designed for different viral dilutions (1 to 12). Two columns were used as duplicates for each viral dilution. Scale .......

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Disclosures

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No conflicts of interest declared.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
VGMSigmaD6429, P0781500 ml DMEM+5 ml Pen/Strepb
PBS ANature pH Phosphate-buffered saline: NaCl 10 g, KCl 0.25 g, Na2HPO4 1.437 g, KH2PO4 0.25 g, and Dist. Water 1 L
AvicellFMCRC-581F2.4 g in 100 ml distilled water dissolved by agitation on a magnetic stirrer for 1 hr. Sterilize by autoclaving
2x DMEMGibco21935-028
TrypsinSigmaT1426
Overlay (10 ml/plate):5 ml 2x DMEM, Trypsin 2 μg/ml final concentration, Avicell 5 ml
Triton X- 100 eSigmaT8787Permeabilization buffer: 0.2% in PBS A (v/v)
Tween 80SigmaP5188Wash Buffer: 0.05% Tween 80 in PBS A (v/v)
Horse serumPAA Labs LtdB15-021ELISA Buffer: 10% in PBS A (v/v) + 0.1% Tween 80
Mouse MAb against influenza type ABioradMCA 4001 st Antibody: 1:1,000 in ELISA Buffer
Goat anti-mouse IgG (H+L) HRP conjugateBiorad172-10112 nd Antibody: 1:1,000 in ELISA Buffer
True Blu peroxidase substrateKPL50-78-02Substrate: True blue +0.03% H2O2 g (1:1,000 of 30% solution)
96-well flat-bottom microtitre platesCostar3596
8 channel multiwall-plate washer and manifoldSigmaM2656
Perfection Plate ScannerEpsonV750 ProThe imaging software can be downloaded freely from http://www.epson.com/cgi-bin/ Store/support/supDetail.jsp? oid=66134&infoType=Downloads.
Software operational environment: LabVIEWNational Instruments CorporationWindow based with NI Vision builderVersion: LabVIEW2012 or above

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Tags

Micro neutralization AssayVirus NeutralizationAntigenic RelationshipInfluenza VirusReceptor destroying EnzymeSerial DilutionCell MonolayerOverlay TechniqueVirus infected CellsNeutralization Titer

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