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Propagation and immunological characterization of coxsackievirus A10 in a serum-free HEK293A cell culture system
Coxsackievirus A10 (CVA10) is one of enteroviral pathogens that cause the hand, foot, and mouth disease (HFMD). Since CVA10 was reported to be not easily propagated in the Vero cell culture, a feasible manufacture process for producing formalin-inactivated CVA10 vaccine is urgently needed. Several c...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10194310/ https://www.ncbi.nlm.nih.gov/pubmed/36958398 http://dx.doi.org/10.1016/j.virusres.2023.199101 |
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author | Lien, Sheng-Chieh Shen, Yu-Sheng Lin, Hsiao-Yu Wu, Shang-Rung Fang, Chih-Yeu Chen, Chi-Hsun Chen, Yi-An Chong, Pele Choi-Sing Huang, Ming-Hsi Chow, Yen-Hung Wang, Jen-Ren Wu, Suh-Chin Liu, Chia-Chyi |
author_facet | Lien, Sheng-Chieh Shen, Yu-Sheng Lin, Hsiao-Yu Wu, Shang-Rung Fang, Chih-Yeu Chen, Chi-Hsun Chen, Yi-An Chong, Pele Choi-Sing Huang, Ming-Hsi Chow, Yen-Hung Wang, Jen-Ren Wu, Suh-Chin Liu, Chia-Chyi |
author_sort | Lien, Sheng-Chieh |
collection | PubMed |
description | Coxsackievirus A10 (CVA10) is one of enteroviral pathogens that cause the hand, foot, and mouth disease (HFMD). Since CVA10 was reported to be not easily propagated in the Vero cell culture, a feasible manufacture process for producing formalin-inactivated CVA10 vaccine is urgently needed. Several cell lines that commonly used for viral vaccine production was tested for CVA10 (M2014 strain) culture in this study, and our result showed that CVA10 could be easily propagated in the HEK293A cells. A serum-free HEK293A cell culture system was developed for CVA10 production and the yields have reached over 10(8) TCID(50)/mL. The biochemical and immunogenic properties of CVA10 particles obtained from this serum-free HEK293A culture were identical to our previous study. Two major particles of CVA10 were separated by ultracentrifugation, and only the infectious mature particles were capable of inducing CVA10 neutralizing antibody responses in the mouse immunogenicity studies. Additionally, we found that coxsackievirus A6 and enterovirus A71 could also be easily propagated using this serum-free HEK293A cell culture system. Our results provide a solution to overcome the obstacle in the propagation of CVA10 and facilitate the development of multivalent vaccines for prevention of HFMD. |
format | Online Article Text |
id | pubmed-10194310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-101943102023-05-19 Propagation and immunological characterization of coxsackievirus A10 in a serum-free HEK293A cell culture system Lien, Sheng-Chieh Shen, Yu-Sheng Lin, Hsiao-Yu Wu, Shang-Rung Fang, Chih-Yeu Chen, Chi-Hsun Chen, Yi-An Chong, Pele Choi-Sing Huang, Ming-Hsi Chow, Yen-Hung Wang, Jen-Ren Wu, Suh-Chin Liu, Chia-Chyi Virus Res Article Coxsackievirus A10 (CVA10) is one of enteroviral pathogens that cause the hand, foot, and mouth disease (HFMD). Since CVA10 was reported to be not easily propagated in the Vero cell culture, a feasible manufacture process for producing formalin-inactivated CVA10 vaccine is urgently needed. Several cell lines that commonly used for viral vaccine production was tested for CVA10 (M2014 strain) culture in this study, and our result showed that CVA10 could be easily propagated in the HEK293A cells. A serum-free HEK293A cell culture system was developed for CVA10 production and the yields have reached over 10(8) TCID(50)/mL. The biochemical and immunogenic properties of CVA10 particles obtained from this serum-free HEK293A culture were identical to our previous study. Two major particles of CVA10 were separated by ultracentrifugation, and only the infectious mature particles were capable of inducing CVA10 neutralizing antibody responses in the mouse immunogenicity studies. Additionally, we found that coxsackievirus A6 and enterovirus A71 could also be easily propagated using this serum-free HEK293A cell culture system. Our results provide a solution to overcome the obstacle in the propagation of CVA10 and facilitate the development of multivalent vaccines for prevention of HFMD. Elsevier 2023-03-24 /pmc/articles/PMC10194310/ /pubmed/36958398 http://dx.doi.org/10.1016/j.virusres.2023.199101 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Lien, Sheng-Chieh Shen, Yu-Sheng Lin, Hsiao-Yu Wu, Shang-Rung Fang, Chih-Yeu Chen, Chi-Hsun Chen, Yi-An Chong, Pele Choi-Sing Huang, Ming-Hsi Chow, Yen-Hung Wang, Jen-Ren Wu, Suh-Chin Liu, Chia-Chyi Propagation and immunological characterization of coxsackievirus A10 in a serum-free HEK293A cell culture system |
title | Propagation and immunological characterization of coxsackievirus A10 in a serum-free HEK293A cell culture system |
title_full | Propagation and immunological characterization of coxsackievirus A10 in a serum-free HEK293A cell culture system |
title_fullStr | Propagation and immunological characterization of coxsackievirus A10 in a serum-free HEK293A cell culture system |
title_full_unstemmed | Propagation and immunological characterization of coxsackievirus A10 in a serum-free HEK293A cell culture system |
title_short | Propagation and immunological characterization of coxsackievirus A10 in a serum-free HEK293A cell culture system |
title_sort | propagation and immunological characterization of coxsackievirus a10 in a serum-free hek293a cell culture system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10194310/ https://www.ncbi.nlm.nih.gov/pubmed/36958398 http://dx.doi.org/10.1016/j.virusres.2023.199101 |
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