Efficacy of Binary Ethylenimine in the Inactivation of Foot-and-Mouth Disease Virus for Vaccine Production in South Korea

被引:8
作者
Kim, Jae Young [1 ]
Park, Sun Young [1 ]
Jin, Jong Sook [1 ]
Kim, Dohyun [1 ]
Park, Jong-Hyeon [1 ]
Park, Sang Hyun [1 ]
Ko, Young-Joon [1 ]
机构
[1] Anim & Plant Quarantine Agcy, Ctr FMD Vaccine Res, 177 Hyeoksin-8-Ro, Gimcheon Si 39660, South Korea
关键词
FMDV; BEI; vaccine;
D O I
10.3390/pathogens12060760
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Foot-and-mouth disease (FMD) vaccines must be produced in a biosafety level 3 facility, so the FMD virus (FMDV) must be completely inactivated after amplification. The inactivation kinetics of FMDV during vaccine antigen production were assessed by evaluating whether the viral titer dropped below 10(-7) TCID50/mL within 24 h of binary ethyleneimine (BEI) treatment. This study dealt with four FMD vaccine candidate strains for the efficacy of BEI treatment at different concentrations and temperatures to determine the optimal inactivation condition of each virus. Two domestic isolates, O/SKR/Boeun/2017 (O BE) and A/SKR/Yeoncheon/2017 (A YC), and two recombinant viruses, PAK/44/2008 (O PA-2) and A22/Iraq/24/64 (A22 IRQ), were investigated. The O BE and A22 IRQ required 2 mM BEI at 26 & DEG;C and 0.5 mM BEI at 37 & DEG;C for complete inactivation. The O PA-2 and A YC required 2 mM BEI at 26 & DEG;C and 1 mM BEI at 37 & DEG;C. Crucially, the yield of FMD virus particles (146S) in the viral infection supernatant was higher (>4.0 & mu;g/mL) than those previously reported; additionally, there was little antigen loss, even after 24 h of treatment with 3 mM BEI. Overall, it is considered economical to produce FMD vaccines using these four kinds of viruses; therefore, these candidate strains will be prioritized for the manufacture of FMD vaccines in South Korea.
引用
收藏
页数:8
相关论文
共 22 条
[1]   Validation of binary ethyleneimine (BEI) used as an inactivant for foot and mouth disease tissue culture vaccine [J].
Aarthi, D ;
Rao, KA ;
Robinson, R ;
Srinivasan, VA .
BIOLOGICALS, 2004, 32 (03) :153-156
[2]   BINARY ETHYLENIMINE AS AN INACTIVANT FOR FOOT-AND-MOUTH-DISEASE VIRUS AND ITS APPLICATION FOR VACCINE PRODUCTION [J].
BAHNEMANN, HG .
ARCHIVES OF VIROLOGY, 1975, 47 (01) :47-56
[3]   INACTIVATION OF VIRAL-ANTIGENS FOR VACCINE PREPARATION WITH PARTICULAR REFERENCE TO THE APPLICATION OF BINARY ETHYLENIMINE [J].
BAHNEMANN, HG .
VACCINE, 1990, 8 (04) :299-303
[4]   SIMPLE METHOD FOR QUANTIFICATION OF 140S PARTICLES OF FOOT-AND-MOUTH-DISEASE VIRUS (FMDV) [J].
BARTELING, SJ ;
MELOEN, RH .
ARCHIV FUR DIE GESAMTE VIRUSFORSCHUNG, 1974, 45 (04) :362-364
[5]   Development and performance of inactivated vaccines against foot and mouth disease [J].
Barteling, SJ .
REVUE SCIENTIFIQUE ET TECHNIQUE-OFFICE INTERNATIONAL DES EPIZOOTIES, 2002, 21 (03) :577-588
[6]   Foot-and-mouth disease vaccination induces cross-reactive IFN-γ responses in cattle that are dependent on the integrity of the 140S particles [J].
Bucafusco, Danilo ;
Di Giacomo, Sebastian ;
Pega, Juan ;
Manuel Schammas, Juan ;
Cardoso, Nancy ;
Victoria Capozzo, Alejandra ;
Perez-Filgueira, Mariano .
VIROLOGY, 2015, 476 :11-18
[7]   Foot-and-mouth disease [J].
Grubman, MJ ;
Baxt, B .
CLINICAL MICROBIOLOGY REVIEWS, 2004, 17 (02) :465-+
[8]   A Vaccine Strain of the A/ASIA/Sea-97 Lineage of Foot-and-Mouth Disease Virus with a Single Amino Acid Substitution in the P1 Region That Is Adapted to Suspension Culture Provides High Immunogenicity [J].
Hwang, Ji-Hyeon ;
Lee, Gyeongmin ;
Kim, Aro ;
Park, Jong-Hyeon ;
Lee, Min Ja ;
Kim, Byounghan ;
Kim, Su-Mi .
VACCINES, 2021, 9 (04)
[9]  
Ismail A., 2013, J. Vet. Adv, V3, P117
[10]   The economic impacts of foot and mouth disease - What are they, how big are they and where do they occur? [J].
Knight-Jones, T. J. D. ;
Rushton, J. .
PREVENTIVE VETERINARY MEDICINE, 2013, 112 (3-4) :161-173