# Single-Domain Antibodies That Specifically Recognize Intact Capsids of Multiple Foot-and-Mouth Disease Serotype O Strains

**Authors:** Michiel M. Harmsen, Nishi Gupta, Quillan Dijkstra, Sandra van de Water, Marga van Setten, Aldo Dekker

PMC · DOI: 10.3390/vaccines13050500 · Vaccines · 2025-05-08

## TL;DR

Researchers developed antibodies that can detect intact virus particles of multiple foot-and-mouth disease strains, improving vaccine quality control.

## Contribution

Four new single-domain antibodies were identified that recognize intact virus particles across multiple serotype O strains.

## Key findings

- Four VHHs (M907F, M910F, M912F, M916F) specifically bind 146S particles of multiple serotype O strains.
- These antibodies bind a conserved antigenic site that changes structure when particles dissociate.
- M916F had the lowest detection limit for three serotype O strains.

## Abstract

Background/Objectives: Intact (146S) foot-and-mouth disease virus (FMDV) particles easily dissociate into 12S particles with a concomitant decreased immunogenicity. Vaccine quality control with 146S-specific single-domain antibodies (VHHs) is hampered by the high strain specificity of most 146S-specific VHHs. This study aimed to isolate 146S-specific VHHs that recognize all serotype O strains. Methods: Biopanning was performed with the FMDV strain O/SKR/7/2010 146S, using a secondary library of mutagenized M170F VHH that did not recognize O/SKR/7/2010 or using phage-display libraries from llamas immunized with other serotype O strains. Novel VHHs were yeast-produced and their strain-, particle-, and antigenic-site specificities were determined by ELISA. Results: M170F mutagenesis did not improve the cross-reaction with O/SKR/7/2010. However, selection from immune libraries resulted in four VHHs that exhibited high 146S specificity for all five serotype O strains analyzed. These VHHs presumably recognize all serotype O strains since the five strains analyzed represent different phylogenetic clades. They bind the same antigenic site as M170F, which was previously shown to be a conserved site in serotypes A and O, and which has an altered 3D structure when 146S dissociates into 12S particles. M916F had the lowest limit of detection, which varied from 0.7 to 5.9 ng/mL 146S particles for three serotype O strains. Conclusions: We identified four VHHs (M907F, M910F, M912F, and M916F) that specifically bind 146S particles of probably all serotype O strains. They enable further improved FMDV vaccine quality control.

## Linked entities

- **Diseases:** foot-and-mouth disease (MONDO:0005765)

## Full-text entities

- **Diseases:** Foot-and-Mouth Disease (MESH:D005536)
- **Chemicals:** 146S (-)
- **Species:** Foot-and-mouth disease virus (no rank) [taxon 12110], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932]
- **Mutations:** M907F, M912F, M170F, M916F, M910F

## Full text

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## Figures

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## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC12116120/full.md

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Source: https://tomesphere.com/paper/PMC12116120