Abstract
Foot-and-mouth disease (FMD) is a highly contagious viral infection causing acute and severe vesicular lesions in cattle and pigs, which has prompted global vaccination policies. This study presents a technique for enhancing antigen yield in SAT1 BOT and SAT3 ZIM by treatment with calcium chloride (CaCl(2)). We tested changes in cell viability in BHK-21 suspension cells treated with varying concentrations of CaCl(2). The optimal CaCl(2) concentration was determined based on antigen yield. The timing of CaCl(2) supplementation relative to FMD virus inoculation was tested. Finally, the optimal medium for antigen production was identified. We observed a concentration-dependent decrease in BHK-21 cell viability at >7.5 mM CaCl(2). A CaCl(2) concentration of 3 mM yielded the most antigens. CaCl(2) supplementation relative to FMD virus infection was optimal 2 h before or with viral inoculation. CD-BHK 21 medium supplemented with CaCl(2) was the most productive medium. Specifically, SAT1 BOT and SAT3 ZIM showed improved antigen production in CD-BHK 21 medium with 3 mM CaCl(2), while Provero-1 and Cellvento BHK-200 media showed no significant enhancement. Overall, CaCl(2) supplementation enhanced FMD antigen productivity. This study provides a useful framework for enhancing antigen production efficiently in the FMD vaccine industry.