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May 9, 2026Viruses0 citationsOpen Access

Evaluation of Antigen Productivity and Inactivation Kinetics of a Recombinant Foot-and-Mouth Disease SAT1 Vaccine Strain

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JKJae Young KimAnimal and Plant Quarantine AgencySPSun Young ParkChonnam National University HospitalGLGyeongmin LeeKorea University

Key Result

The SAT1 BOT-R strain vaccine elicited neutralizing antibody responses in pigs with a median titer of 1:500 following booster immunization, demonstrating its viability for domestic vaccine production.

Key Points

  • This study aims to assess the SAT1 BOT-R strain as a candidate vaccine for domestic production against foot-and-mouth disease virus.
  • Evaluated optimal antigen production conditions for the SAT1 BOT-R strain.
  • Determined virus inactivation parameters using binary ethylenimine.
  • Examined immunogenicity of the vaccine in pigs.
  • Optimal antigen yield achieved at 20-24 hours post-infection with 0.005-0.01 multiplicity of infection, reaching 9.5 μg/mL.
  • Complete virus inactivation at 2 mM binary ethylenimine for 24 hours at 26 °C.
  • Vaccines developed from both production methods elicited neutralizing antibody responses with a median titer of 1:500.

Structured PICO

P
Population
Pigs and cell culture models for foot-and-mouth disease virus (FMDV) SAT1 BOT-R strain
I
Intervention
SAT1 BOT-R strain vaccine formulation (flask- and bioreactor-derived antigens)
O
Outcome
Antigen yield, virus inactivation parameters, and immunogenicity (neutralizing antibody responses)surrogate

The SAT1 BOT-R strain is a viable and scalable candidate for FMDV SAT1 antigen banking and domestic vaccine production.

Abstract

The Republic of Korea has implemented routine vaccination against foot-and-mouth disease virus (FMDV) in livestock using a bivalent vaccine comprising serotypes O and A following the massive FMD outbreak in 2010, while antigens for the remaining serotypes are maintained in overseas antigen banks. The recent geographic expansion of FMDV Southern African Territories 1 (SAT1) beyond Africa underscores the need for enhanced preparedness in previously unaffected regions. In this study, we evaluated the SAT1 BOT-R strain as a candidate vaccine seed for potential domestic vaccine production by optimizing antigen production conditions, assessing scalability, determining virus inactivation parameters, and examining immunogenicity in pigs. Optimal antigen yield was achieved at 20 h−24 h post infection with a multiplicity of infection of 0.005−0.01, with production remaining stable under mildly alkaline conditions. Antigen productivity was consistently maintained during scale-up from shake flasks to a bioreactor, yielding up to 9.5 μg/mL. Complete virus inactivation was achieved using binary ethylenimine at 2 mM for 24 h at 26 °C. Vaccines formulated from both flask- and bioreactor-derived antigens elicited comparable neutralizing antibody responses in pigs, reaching a median titer of 1:500 following booster immunization. Collectively, these findings demonstrate that the SAT1 BOT-R strain is a viable and scalable candidate for SAT1 antigen banking and future domestic vaccine production, providing a practical framework for strengthening national preparedness against potential incursions of FMDV SAT1.

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Cite This Study

Kim et al. (2026) studied Foot-and-mouth disease virus (FMDV) SAT1. SAT1 BOT-R strain vaccine was evaluated on Antigen yield, virus inactivation, and neutralizing antibody responses. The SAT1 BOT-R strain vaccine elicited neutralizing antibody responses in pigs with a median titer of 1:500 following booster immunization, demonstrating its viability for domestic vaccine production.

synapsesocial.com/papers/69fed03cb9154b0b8287739fhttps://doi.org/10.3390/v18050537
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Also Consider

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

  1. 1Evaluation of an In-House Developed Foot-and-Mouth Disease Virus SAT 3 Vaccine Strain Based on Antigen Productivity and Inactivation Kinetics for Commercial Feasibility2026
  2. 2Evaluation of Foot-and-Mouth Disease (FMD) Virus Asia1 Genotype-V as an FMD Vaccine Candidate: Study on Vaccine Antigen Production Yield and Inactivation Kinetics2024 · 3 citations
  3. 3Production of Foot-and-Mouth Disease Type O and A Vaccine Antigens on a Pilot Scale and Determination of Optimal Amount of Antigen for Monovalent Vaccines2023 · 1 citations
  4. 4Comprehensive evaluation of an emergency monovalent SAT1 foot-and-mouth-disease vaccine: Antigen quality, product consistency, and protective efficacy2026
  5. 5Determination of Optimal Antigen Yield and Virus Inactivation Conditions for the Production of the Candidate Foot-and-Mouth Disease Recombinant Vaccine Strain Asia1 Shamir-R in a Bioreactor2024 · 2 citations