Improving Foot and Mouth Vaccine Stability Using HPSEC
Researchers from the Chinese Academy of Science in Beijing, China, have used high‑performance size-exclusion chromatography (HPSEC) and differential scanning calorimetry (DSC) to study the stabilization of inactivated foot and mouth disease virus.
Photo Credit: ArtemZ/Shutterstock.com
Researchers from the Chinese Academy of Science in Beijing, China, have used highâperformance size-exclusion chromatography (HPSEC) and differential scanning calorimetry (DSC) to study the stabilization of inactivated foot and mouth disease virus (1).
Highly contagious and economically devastating, foot and mouth disease (FMD) is synonymous with mass livestock cullings and exclusion zones. Affecting clovenâhoofed animals such as cattle, swine, sheep, and goats, the virus has emerged numerous times around the globe. Notable outbreaks occurred in the UK in 2001 and 2007 costing the British agricultural economy billions in lost revenue; in mainland China FMD outbreaks have regularly been covered up leaving the true global scale of FMD infection a complete mystery.
Given the enormous damage this virus is capable of, efforts to create new vaccines for emerging strains have intensified. Recombinant protein and peptide vaccines have recently been reported (2,3), however, these have so far not been as effective as the conventional inactivated virus products (4). Poor stability of the inactivated FMD vaccine (FMDV) is a considerable challenge to its production, requiring cold chain transportation and storage, therefore increasing costs and making FMD vaccination difficult in areas where the environment is harsh. Researchers attempted to identify the best condition for stabilizing FMDV using HPSEC and DSC.
Results indicated a pH of 7.5–8.0 with an excipient of 20% sucrose and glycerol offered the best protection. It significantly prolonged the half-life of the vaccine at 45 °C from less than 30 min to more than 3 days, allowing transportation and storage of the recombinant protein vaccine under harsh conditions and increasing its viability as an effective vaccine option.
References
- Y. Yang et al., Vaccine35, 2413–2419 (2017).
- B. Mohana Subramanian et al., Antiviral Res.96, 288–295 (2012).
- Z. Li et al., Plos One7, e43849 (2012).
- M.A. Spitteler et al., Vaccine29, 7182–7187 (2011).
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