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Viral intra-host evolutionary dynamics revealed via serial passage of Japanese encephalitis virus in vitro
Analyses of viral inter- and intra-host mutations could better guide the prevention and control of infectious diseases. For a long time, studies on viral evolution have focused on viral inter-host variations. Next-generation sequencing has accelerated the investigations of viral intra-host diversity...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10185921/ https://www.ncbi.nlm.nih.gov/pubmed/37205166 http://dx.doi.org/10.1093/ve/veac103 |
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author | Sun, Bangyao Ni, Ming Liu, Haizhou Liu, Di |
author_facet | Sun, Bangyao Ni, Ming Liu, Haizhou Liu, Di |
author_sort | Sun, Bangyao |
collection | PubMed |
description | Analyses of viral inter- and intra-host mutations could better guide the prevention and control of infectious diseases. For a long time, studies on viral evolution have focused on viral inter-host variations. Next-generation sequencing has accelerated the investigations of viral intra-host diversity. However, the theoretical basis and dynamic characteristics of viral intra-host mutations remain unknown. Here, using serial passages of the SA14-14-2 vaccine strain of Japanese encephalitis virus (JEV) as the in vitro model, the distribution characteristics of 1,788 detected intra-host single-nucleotide variations (iSNVs) and their mutated frequencies from 477 deep-sequenced samples were analyzed. Our results revealed that in adaptive (baby hamster kidney (BHK)) cells, JEV is under a nearly neutral selection pressure, and both non-synonymous and synonymous mutations represent an S-shaped growth trend over time. A higher positive selection pressure was observed in the nonadaptive (C6/36) cells, and logarithmic growth in non-synonymous iSNVs and linear growth in synonymous iSNVs were observed over time. Moreover, the mutation rates of the NS4B protein and the untranslated region (UTR) of the JEV are significantly different between BHK and C6/36 cells, suggesting that viral selection pressure is regulated by different cellular environments. In addition, no significant difference was detected in the distribution of mutated frequencies of iSNVs between BHK and C6/36 cells. |
format | Online Article Text |
id | pubmed-10185921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101859212023-05-17 Viral intra-host evolutionary dynamics revealed via serial passage of Japanese encephalitis virus in vitro Sun, Bangyao Ni, Ming Liu, Haizhou Liu, Di Virus Evol Research Article Analyses of viral inter- and intra-host mutations could better guide the prevention and control of infectious diseases. For a long time, studies on viral evolution have focused on viral inter-host variations. Next-generation sequencing has accelerated the investigations of viral intra-host diversity. However, the theoretical basis and dynamic characteristics of viral intra-host mutations remain unknown. Here, using serial passages of the SA14-14-2 vaccine strain of Japanese encephalitis virus (JEV) as the in vitro model, the distribution characteristics of 1,788 detected intra-host single-nucleotide variations (iSNVs) and their mutated frequencies from 477 deep-sequenced samples were analyzed. Our results revealed that in adaptive (baby hamster kidney (BHK)) cells, JEV is under a nearly neutral selection pressure, and both non-synonymous and synonymous mutations represent an S-shaped growth trend over time. A higher positive selection pressure was observed in the nonadaptive (C6/36) cells, and logarithmic growth in non-synonymous iSNVs and linear growth in synonymous iSNVs were observed over time. Moreover, the mutation rates of the NS4B protein and the untranslated region (UTR) of the JEV are significantly different between BHK and C6/36 cells, suggesting that viral selection pressure is regulated by different cellular environments. In addition, no significant difference was detected in the distribution of mutated frequencies of iSNVs between BHK and C6/36 cells. Oxford University Press 2023-03-28 /pmc/articles/PMC10185921/ /pubmed/37205166 http://dx.doi.org/10.1093/ve/veac103 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sun, Bangyao Ni, Ming Liu, Haizhou Liu, Di Viral intra-host evolutionary dynamics revealed via serial passage of Japanese encephalitis virus in vitro |
title | Viral intra-host evolutionary dynamics revealed via serial passage of Japanese encephalitis virus in vitro |
title_full | Viral intra-host evolutionary dynamics revealed via serial passage of Japanese encephalitis virus in vitro |
title_fullStr | Viral intra-host evolutionary dynamics revealed via serial passage of Japanese encephalitis virus in vitro |
title_full_unstemmed | Viral intra-host evolutionary dynamics revealed via serial passage of Japanese encephalitis virus in vitro |
title_short | Viral intra-host evolutionary dynamics revealed via serial passage of Japanese encephalitis virus in vitro |
title_sort | viral intra-host evolutionary dynamics revealed via serial passage of japanese encephalitis virus in vitro |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10185921/ https://www.ncbi.nlm.nih.gov/pubmed/37205166 http://dx.doi.org/10.1093/ve/veac103 |
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