Optimized production of CD2V extracellular domain of African swine fever virus on adherent culture baculovirus- Sf9 insect cell system
Author affiliations
DOI:
https://doi.org/10.15625/vjbt-21868Keywords:
Baculovirus expression vector system, insect cell, CD2v, Sf9, multiplicity of infection, time of harvestAbstract
The baculovirus expression vector system (BEVS) is one of the strongest tools for producing recombinant proteins such as pharmaceuticals and vaccines. In this study, the multivalent CD2v extracellular domain (CD2v ED) of the African swine fever virus (ASFV) was expressed in Sf9 insect cells using BEVs. Bacmid carrying the gene encoding CD2v ED-Foldon-His was transfected into Sf9 insect cells using the lipid transfer complex Cellfectin II and Opti-MEM I Reduced Serum Medium. The transfection process was observed under microscopy and protein expression would be assessed by western blot. The results indicated the transparent differences in infected cells, including the swelling of cells, the increase of nuclei, granular and vesicular appearance, cessation of cell growth, detachment from the flask bottom, and cell lysis in comparison with normal cells that are round, small, and regular size. The western blot results illustrated the expression of CD2v ED-Foldon-His in trimeric and oligomeric forms with bands of 100 kDa and more than 250 kDa, respectively. Most importantly, the expression of CD2v ED-Foldon-His in adherent culture insect cells was optimized with two main factors, namely multiplicity of infection (MOI) and infection time. The results demonstrated the highest yield of CD2v ED-Foldon-His protein was 4.4 mg/L at a MOI of 5 pfu/cell and 5 days post-infection, which was confirmed by captured pictures throughout the infection time. This is the first study on the expression of the oligomeric CD2v extracellular domain on a baculovirus-insect cell system, aiming to produce subunit vaccines against ASFV. Besides, the study also presented a practical procedure for enhancing the expression of recombinant proteins in this system.
Downloads
References
Argilaguet, J. M., Pérez, M. E., López, S., Goethe, M., Escribano, J. M., Giesow, K., et al. (2013). BacMam immunization partially protects pigs against sublethal challenge with African swine fever virus. Antiviral Research 98(1), 61–65. https://doi.org/10.1016/j.antiviral.2013.02.005
Argilaguet, J. M., Perez, M. E., Nofrarıas, M., Gallardo, C., Accensi, F., Lacasta, A., et al. (2012). DNA vaccination partially protects against African swine fever virus lethal challenge in the absence of antibodies. PLoS ONE, 7(9), 1–11. https://doi.org/10.1371/journal.pone.0040942
Aung, S. M., Kanokwiroon, K., Phairatana, T., and Chatpun, S. (2019). Live and dead cells counting from microscopic trypan blue staining images using thresholding and morphological operation techniques. International Journal of Electrical and Computer Engineering, 9(4), 2460–2468. https://doi.org/10.11591/ijece.v9i4.pp2460-2468
Borca, M. V., Carrillo, C., Zsak, L., Laegreid, W. W., Kutish, G. F., Neilan, J. G., et al. (1998). Deletion of a CD2-like gene, 8-DR, from African swine fever virus affects viral infection in domestic swine. Journal of Virology, 72(4), 2881–2889. https://doi.org/10.1128/jvi.72.4.2881-2889.1998
Chambers, A. C., Aksular, M., Graves, L. P., Irons, S. L., Possee, R. D., and King, L. A. (2018). Overview of the Baculovirus Expression System. Current Protocols in Protein Science, 91(1), 5.4.1-5.4.6. https://doi.org/10.1002/cpps.47
Dixon, L. K., Abrams, C. C., Bowick, G., Goatley, L. C., Kay-Jackson, P. C., Chapman, D., et al. (2004). African swine fever virus proteins involved in evading host defence systems. Veterinary Immunology and Immunopathology, 100(3–4), 117–134. https://doi.org/10.1016/j.vetimm.2004.04.002
Dixon, L. K., Chapman, D. A. G., Netherton, C. L., and Upton, C. (2013). African swine fever virus replication and genomics. Virus Research, 173(1), 3–14. https://doi.org/10.1016/j.virusres.2012.10.020
Dixon, L. K., Islam, M., Nash, R., and Reis, A. L. (2019). African swine fever virus evasion of host defences. Virus Research, 266(April), 25–33. https://doi.org/10.1016/j.virusres.2019.04.002
Do, D. T., Trong, M. V., Luu, C. A., Anh, N. D., Pham, T. H., Le, M. T. Q., et al. (2021). Establishing a process for cultivation and purification of baculovirus carrying the spiky protein (protein s) of Sar-Cov-2 to produce Covid-19 vaccine on baculovirus platforms on laboratory scale. Vietnam Journal of Preventive Medicine, 31(9), 39–52. https://doi.org/10.51403/0868-2836/2021/472
Druzinec, D., Salzig, D., Brix, A., Kraume, M., Vilcinskas, A., Kollewe, C., et al. (2013). Optimization of insect cell-based protein production processes - online monitoring, expression systems, scale up. Advances in Biochemical Engineering/Biotechnology, 136, 65–100. https://doi.org/10.1007/10
Falak, R., Varasteh, A. R., Ketabdar, H., and Sankian, M. (2014). Expression of grape class IV chitinase in Spodoptera frugiperda (Sf9) insect cells. Allergologia et Immunopathologia, 42(4), 293–301. https://doi.org/10.1016/j.aller.2012.11.004
Feng, Z., Chen, J., Liang, W., Chen, W., Li, Z., Chen, Q., et al. (2020). The recombinant pseudorabies virus expressing African swine fever virus CD2v protein is safe and effective in mice. Virology Journal, 1–17. https://doi.org/10.1186/s12985-020-01450-7
Harbury, P. B., Zhang, T., Kim, P. S., and Alber, T. (1993). A switch between two-, three-, and four-stranded coiled coils in GCN4 leucine zipper mutants. Science, 262(5138), 1401–1407. https://doi.org/10.1126/science.824877
Jia, N., Ou, Y., Pejsak, Z., Zhang, Y., and Zhang, J. (2017). Roles of African swine fever virus structural proteins in viral infection. Journal of Veterinary Research (Poland), 61(2), 135–143. https://doi.org/10.1515/jvetres-2017-0017
Käßer, L., Harnischfeger, J., Salzig, D., and Czermak, P. (2022). The effect of different insect cell culture media on the efficiency of protein production by Spodoptera frugiperda cells. Electronic Journal of Biotechnology, 56, 54–64. https://doi.org/10.1016/j.ejbt.2022.01.004
Le, V. P., Jeong, D. G., Yoon, S., Kwon, H., Bich, T., Trinh, N., et al. (2019). Outbreak of African swine fever, Vietnam, 2019. Emerging Infectious Diseases, 25(7), 1433–1435. https://doi.org/10.3201/eid2507.190303
Li, Z., Chen, W., Qiu, Z., Li, Y., Fan, J., Wu, K.,et al. (2022). African swine fever virus: A review. Life, 12(8), 1–41. https://doi.org/10.3390/life12081255
Mendoza, E. J., Manguiat, K., Wood, H., and Drebot, M. (2020). Two detailed plaque assay protocols for the quantification of infectious SARS-CoV-2. Current Protocols in Microbiology, 57(1), 1–15. https://doi.org/10.1002/cpmc.105
Nguyen, G. T., Le, T. T., Vu, S. D. T., Nguyen, T. T., Le, M. T. T., Pham, V. T., et al. (2024). A plant-based oligomeric CD2v extracellular domain antigen exhibits equivalent immunogenicity to the live attenuated vaccine ASFV-G-∆I177L. Medical Microbiology and Immunology, 213(1), 22. https://doi.org/10.1007/s00430-024-00804-0
Nguyen, G. T., Tran, L. N, Nguyen, H. T. T., Le, T. T., and Pham, N. B. (2024). Vector construction for African swine fever virus CD2v antigen expression on baculovirus–insect cell system, using the Q5-site-directed mutagenesis kit. TNU Journal of Science and Technology, 229(05), 129–136. https://doi.org/10.34238/tnu-jst.9236
Pérez, N. D., García, U. E., Martínez, B. M., Nogal, M. L., Barroso, S., Revilla, Y., et al. (2015). CD2v interacts with adaptor protein AP-1 during African swine fever infection. PLoS ONE, 10(4), 1–19. https://doi.org/10.1371/journal.pone.0123714
Phan, H. T., Ho, T. T., Chu, H. H., Vu, T. H., Gresch, U., et al. (2017). Neutralizing immune responses induced by oligomeric H5N1-hemagglutinins from plants. Veterinary Research, 48(1), 1–13. https://doi.org/10.1186/s13567-017-0458-x
Ruiz, G. F., Rodri´Guez, F., and Escribano, J. M. (1996). Functional and immunological properties of the baculovirus-expressed hemagglutinin of African swine fever virus. Virology, 289(218), 285–289. https://doi.org/10.1006/viro.1996.0193
Salas, M. L., and Andrés, G. (2012). African swine fever virus morphogenesis. Virus Research, 1–13. https://doi.org/10.1016/j.virusres.2012.09.016
Sánchez-Cordón, P. J., Jabbar, T., Berrezaie, M., Chapman, D., Reis, A., Sastre, P., et al. (2018). Evaluation of protection induced by immunisation of domestic pigs with deletion mutant African swine fever virus BeninΔMGF by different doses and routes. Vaccine, 36(5), 707–715. https://doi.org/10.1016/j.vaccine.2017.12.030
Stolt-Bergner, P., Benda, C., Bergbrede, T., Besir, H., Celie, P. H. N., Chang, C., et al. (2018). Baculovirus-driven protein expression in insect cells: A benchmarking study. Journal of Structural Biology, 203(2), 71–80. https://doi.org/10.1016/j.jsb.2018.03.004
Tao, Y., Strelkov, S. V, Mesyanzhinov, V. V, and Rossmann, M. G. (1997). Structure of bacteriophage T4 fibritin: a segmented coiled coil and the role of the C-terminal domain. Structure, 5(6), 789–798. https://doi.org/10.1016/s0969-2126(97)00233-5
Teklue, T., Wang, T., Luo, Y., Hu, R., Sun, Y., and Qiu, H. (2020). Generation and evaluation of an African swine fever virus mutant with deletion of the CD2V and UK genes. Vaccines, 8(763), 1–17. https://doi.org/10.1016/j.antiviral.2013.02.005
Zitzmann, J., Sprick, G., Weidner, T., Schreiber, C., and Czermak, P. (2017). New Insights into Cell Culture Technology (1st ed.). Intech. https://doi.org/10.5772/67849
Downloads
Published
How to Cite
Issue
Section
Funding data
-
Vietnam Academy of Science and Technology
Grant numbers NVCC08.07/24-24