Therapeutic potential of the neutralizing monoclonal antibody 45G3 against encephalomyocarditis virus
Yanfang Zhang, Zhiying Wang, Yaohui Fang, Qiong Zhu, Jie Fu, Sijing Hu, Jiayin Jin, Min Zhou, Xijia Liu, Danna Zhang, Shouwei Huang, Yali Deng, Lingling Xie, Shu Shen, Jing Ye, Fei Deng, Shengbo Cao
Animal Diseases ›› 2025, Vol. 5 ›› Issue (1) : 1.
Therapeutic potential of the neutralizing monoclonal antibody 45G3 against encephalomyocarditis virus
Encephalomyocarditis virus (EMCV), a potential zoonotic pathogen, poses significant socioeconomic and public health challenges across various host species. Although EMCV rarely triggers severe clinical symptoms in humans, its widespread prevalence and unique biological characteristics underscore the need for continuous surveillance and the development of effective therapeutics and prophylactics. In this study, we evaluated the neutralizing effects of a monoclonal antibody derived from the spleens of mice immunized with EMCV virus-like particles (VLPs), both in vitro and in vivo. Using recombinant DNA technology, we engineered a baculovirus system to express EMCVs P12A and 3C, facilitating the production of VLPs in Sf9 cells. These VLPs serve as antigens to immunize mice, leading to the isolation of the monoclonal antibody 45G3. This antibody exhibited high specificity for EMCV conformational epitopes, excluding linear epitopes, and demonstrated potent in vitro neutralizing activity, with an IC50 of 0.01873 μg/mL. Immunoelectron microscopy (IEM) revealed a strong direct interaction between the 45G3 antibody and EMCV particles. Virus adsorption inhibition assays demonstrated that 45G3 effectively blocked viral attachment, thereby preventing further infection of host cells. These findings further support the notion of a robust interaction between the virus and the antibody. Moreover, in vivo assessments revealed that 45G3 significantly reduced viral loads in treated mice and improved survival outcomes following EMCV exposure. Additionally, posttreatment analysis revealed reduced tissue damage and a markedly decreased inflammatory response in the brain, indicating that the 45G3 antibody effectively blocked viral infection, thereby mitigating tissue damage and enhancing survival. These findings position 45G3 as a promising candidate for EMCV management and provide a strong foundation for the future development of antiviral drugs targeting this widespread virus.
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|
[] |
Camp, J.V., Desvars-Larrive, A., 2022. Monitoring urban zoonotic virus activity: Are city rats a promising surveillance tool for emerging viruses? Viruses 14 (7). https://doi.org/10.3390/v14071516.
|
[] |
|
[] |
Cardeti, G., V. Mariano, C. Eleni, M. Aloisi, G. Grifoni, S. Sittinieri, G. Dante, V. Antognetti, E. A. Foglia, A. Cersini, and A. Nardi. 2016. Encephalomyocarditis virus infection in Macaca sylvanus and Hystrix cristata from an Italian rescue center for wild and exotic animals. Virology Journal 13 (1): 193. https://doi.org/10.1186/s12985-016-0653-9.
|
[] |
|
[] |
|
[] |
Cherry, S., 2019. Encephalomyocarditis virus entry unveiled. mBio 10 (2). https://doi.org/10.1128/mBio.00305-19.
|
[] |
Czechowicz, J., Huaman, J.L., Forshey, B.M., Morrison, A.C., Castillo, R., Huaman, A., Caceda, R., Eza, D., Rocha, C., Blair, P.J., Olson, J.G., Kochel, T.J., 2011. Prevalence and risk factors for encephalomyocarditis virus infection in Peru. Vector borne and zoonotic diseases (Larchmont, N.Y.) 11 (4), 367–374. https://doi.org/10.1089/vbz.2010.0029.
|
[] |
Dea, S., Bilodeau, R., Sauvageau, R., Martineau, G.P., 1991. Outbreaks in Quebec pig farms of respiratory and reproductive problems associated with encephalomyocarditis virus. Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc. 3 (4), 275–282. https://doi.org/10.1177/104063879100300401.
|
[] |
|
[] |
|
[] |
|
[] |
|
[] |
|
[] |
Guo, C., D. Reus, J. D. Coey, S. Sukumar, B. Lang, J. Mclauchlan, S. Boulant, M. L. Stanifer, and C. G. G. Bamford. 2021. Conserved Induction of Distinct Antiviral Signalling Kinetics by Primate Interferon Lambda 4 Proteins. Front Immunol 12:772588. https://doi.org/10.3389/fimmu.2021.772588.
|
[] |
Han, Y., Xie, J., Xu, S., Bi, Y., Li, X., Zhang, H., Idris, A., Bai, J., Feng, R., 2021. Encephalomyocarditis virus abrogates the interferon beta signaling pathway via its structural protein VP2. Journal of virology 95 (6). https://doi.org/10.1128/jvi.01590-20.
|
[] |
Han, R., Liang, L., Qin, T., Xiao, S., Liang, R., 2022. Encephalomyocarditis virus 2A protein inhibited apoptosis by interaction with annexin A2 through JNK/c-Jun pathway. Viruses 14 (2). https://doi.org/10.3390/v14020359.
|
[] |
Han, W., Zhang, J., Li, M., An, M., Li, L., 2023. Analysis of chromatin accessibility changes induced by BMMC recognition of foot-and-mouth disease virus-like particles through ATAC-seq. International journal of molecular sciences 24 (23). https://doi.org/10.3390/ijms242317044.
|
[] |
Helwig, F.C., Schmidt, C.H., 1945. A filter-passing agent producing interstitial myocarditis in anthropoid apes and small animals. Science (New York, N.Y.) 102 (2637), 31–33. https://doi.org/10.1126/science.102.2637.31.
|
[] |
Hu, S., Zha, Y., Yang, W., Cui, K., 2022. Dysregulation of NK and CD8(+)T Cells by the microbiota promotes the progression of lung cancer. 2022 7057089. https://doi.org/10.1155/2022/7057089.
|
[] |
|
[] |
|
[] |
|
[] |
|
[] |
Luo, Y. K., L. Liang, Q. H. Tang, L. Zhou, L. J. Shi, Y. Y. Cong, W. C. Lin, and S. J. Cui. 2017. Isolation and characterization of encephalomyocarditis virus from dogs in China. Science and Reports 7 (1): 438. https://doi.org/10.1038/s41598-017-00435-x.
|
[] |
|
[] |
|
[] |
Murnane, T.G., Craighead, J.E., Mondragon, H., Shelokov, A., 1960. Fatal disease of swine due to encephalomyocarditis virus. Science (New York, N.Y.) 131 (3399), 498–499. https://doi.org/10.1126/science.131.3399.498.
|
[] |
O’connor, T. W., D. S. Finlaison, L. K. Manning, M. S. Hazelton, Z. B. Spiers, P. Pinczowski, E. M. Bolin, P. D. Kemsley, N. U. Horadagoda, A. J. Dart, et al. 2020. Encephalomyocarditis virus infection in alpacas. Australian Veterinary Journal 98 (10): 486–490. https://doi.org/10.1111/avj.12962.
|
[] |
|
[] |
|
[] |
Romey, A., Lamglait, B., Blanchard, Y., Touzain, F., Quenault, H., Relmy, A., Zientara, S., Blaise-Boisseau, S., Bakkali-Kassimi, L., 2021. Molecular characterization of encephalomyocarditis virus strains isolated from an African elephant and rats in a French zoo. Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc. 33 (2), 313–321. https://doi.org/10.1177/1040638720978389.
|
[] |
Salogni, C., Lazzaro, M., Giacomini, E., Giovannini, S., Zanoni, M., Giuliani, M., Ruggeri, J., Pozzi, P., Pasquali, P., Boniotti, M.B., Alborali, G.L., 2016. Infectious agents identified in aborted swine fetuses in a high-density breeding area: a three-year study. Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc. 28 (5), 550–554. https://doi.org/10.1177/1040638716656024.
|
[] |
|
[] |
Sherry, L., Grehan, K., Snowden, J.S., Knight, M.L., Adeyemi, O.O., Rowlands, D.J., Stonehouse, N.J., 2020. Comparative molecular biology approaches for the production of poliovirus virus-like particles using pichia pastoris. mSphere 5 (2). https://doi.org/10.1128/mSphere.00838-19.
|
[] |
|
[] |
|
[] |
|
[] |
|
[] |
|
[] |
Zhang, Z.D., Xiong, T.C., Yao, S.Q., Wei, M.C., Chen, M., Lin, D., 2020. RNF115 plays dual roles in innate antiviral responses by catalyzing distinct ubiquitination of MAVS and MITA. 11 (1), 5536. https://doi.org/10.1038/s41467-020-19318-3.
|
[] |
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