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Comparison of antigenic mutation during egg and cell passage cultivation of H3N2 influenza virus

PURPOSE: When influenza viruses are cultured in eggs, amino acid mutations of the hemagglutinin may occur through egg adaptation. On the other hand, when influenza viruses are cultured in animal cells, no antigenic mutation occurs unlike in eggs. Therefore, we examined whether the antigenic mutation...

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Autores principales: Park, Yong Wook, Kim, Yun Hee, Jung, Hwan Ui, Jeong, Oh Seok, Hong, Eun Ji, Kim, Hun, Lee, Jae Il
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Vaccine Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7024727/
https://www.ncbi.nlm.nih.gov/pubmed/32095441
http://dx.doi.org/10.7774/cevr.2020.9.1.56
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author Park, Yong Wook
Kim, Yun Hee
Jung, Hwan Ui
Jeong, Oh Seok
Hong, Eun Ji
Kim, Hun
Lee, Jae Il
author_facet Park, Yong Wook
Kim, Yun Hee
Jung, Hwan Ui
Jeong, Oh Seok
Hong, Eun Ji
Kim, Hun
Lee, Jae Il
author_sort Park, Yong Wook
collection PubMed
description PURPOSE: When influenza viruses are cultured in eggs, amino acid mutations of the hemagglutinin may occur through egg adaptation. On the other hand, when influenza viruses are cultured in animal cells, no antigenic mutation occurs unlike in eggs. Therefore, we examined whether the antigenic mutations actually occurred after passage of H3N2 (A/Texas/50/2012) virus up to 15 times in eggs and MDCK-Sky3851 cells. MATERIALS AND METHODS: Prototype A/Texas/50/2012 (H3N2) influenza virus which was isolated from clinical patient, not passaged in egg, was obtained and propagated using the specific pathogen free egg and the MDCK-Sky3851 cell line up to 15 passage, and the changes in the antigen sequence of the influenza viruses were confirmed by gene sequencing and protein structure analysis. RESULTS: In term of the hemagglutination titer of influenza virus, the reactivity to chicken and guinea pig red blood cell showed different results between egg propagated and cell propagated viruses. In the sequence analysis results for hemagglutinin and neuraminidase, no antigenic mutation was observed throughout all passages when cultured in MDCK-Sky3851 cells. On the other hand, mutations occurred in three amino acid sequences (H156R, G186S, S219F) in hemagglutinin up to 15 passages when cultured in eggs. CONCLUSION: H3N2 influenza virus cultured in eggs could lead mutations in amino acid sequence of hemagglutinin, distinct from the corresponding virus cultured in cells for which no antigenic mutation was observed. These findings suggest that cell culture is a more stable and effective way of production with lower risk of antigenic mutations for the manufacture of influenza vaccines.
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spelling pubmed-70247272020-02-24 Comparison of antigenic mutation during egg and cell passage cultivation of H3N2 influenza virus Park, Yong Wook Kim, Yun Hee Jung, Hwan Ui Jeong, Oh Seok Hong, Eun Ji Kim, Hun Lee, Jae Il Clin Exp Vaccine Res Original Article PURPOSE: When influenza viruses are cultured in eggs, amino acid mutations of the hemagglutinin may occur through egg adaptation. On the other hand, when influenza viruses are cultured in animal cells, no antigenic mutation occurs unlike in eggs. Therefore, we examined whether the antigenic mutations actually occurred after passage of H3N2 (A/Texas/50/2012) virus up to 15 times in eggs and MDCK-Sky3851 cells. MATERIALS AND METHODS: Prototype A/Texas/50/2012 (H3N2) influenza virus which was isolated from clinical patient, not passaged in egg, was obtained and propagated using the specific pathogen free egg and the MDCK-Sky3851 cell line up to 15 passage, and the changes in the antigen sequence of the influenza viruses were confirmed by gene sequencing and protein structure analysis. RESULTS: In term of the hemagglutination titer of influenza virus, the reactivity to chicken and guinea pig red blood cell showed different results between egg propagated and cell propagated viruses. In the sequence analysis results for hemagglutinin and neuraminidase, no antigenic mutation was observed throughout all passages when cultured in MDCK-Sky3851 cells. On the other hand, mutations occurred in three amino acid sequences (H156R, G186S, S219F) in hemagglutinin up to 15 passages when cultured in eggs. CONCLUSION: H3N2 influenza virus cultured in eggs could lead mutations in amino acid sequence of hemagglutinin, distinct from the corresponding virus cultured in cells for which no antigenic mutation was observed. These findings suggest that cell culture is a more stable and effective way of production with lower risk of antigenic mutations for the manufacture of influenza vaccines. The Korean Vaccine Society 2020-01 2020-01-31 /pmc/articles/PMC7024727/ /pubmed/32095441 http://dx.doi.org/10.7774/cevr.2020.9.1.56 Text en © Korean Vaccine Society. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Park, Yong Wook
Kim, Yun Hee
Jung, Hwan Ui
Jeong, Oh Seok
Hong, Eun Ji
Kim, Hun
Lee, Jae Il
Comparison of antigenic mutation during egg and cell passage cultivation of H3N2 influenza virus
title Comparison of antigenic mutation during egg and cell passage cultivation of H3N2 influenza virus
title_full Comparison of antigenic mutation during egg and cell passage cultivation of H3N2 influenza virus
title_fullStr Comparison of antigenic mutation during egg and cell passage cultivation of H3N2 influenza virus
title_full_unstemmed Comparison of antigenic mutation during egg and cell passage cultivation of H3N2 influenza virus
title_short Comparison of antigenic mutation during egg and cell passage cultivation of H3N2 influenza virus
title_sort comparison of antigenic mutation during egg and cell passage cultivation of h3n2 influenza virus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7024727/
https://www.ncbi.nlm.nih.gov/pubmed/32095441
http://dx.doi.org/10.7774/cevr.2020.9.1.56
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