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Predicting Egg Passage Adaptations to Design Better Vaccines for the H3N2 Influenza Virus
Seasonal H3N2 influenza evolves rapidly, leading to an extremely poor vaccine efficacy. Substitutions employed during vaccine production using embryonated eggs (i.e., egg passage adaptation) contribute to the poor vaccine efficacy (VE), but the evolutionary mechanism remains elusive. Using an unprec...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9501976/ https://www.ncbi.nlm.nih.gov/pubmed/36146872 http://dx.doi.org/10.3390/v14092065 |
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author | Liu, Yunsong Chen, Hui Duan, Wenyuan Zhang, Xinyi He, Xionglei Nielsen, Rasmus Ma, Liang Zhai, Weiwei |
author_facet | Liu, Yunsong Chen, Hui Duan, Wenyuan Zhang, Xinyi He, Xionglei Nielsen, Rasmus Ma, Liang Zhai, Weiwei |
author_sort | Liu, Yunsong |
collection | PubMed |
description | Seasonal H3N2 influenza evolves rapidly, leading to an extremely poor vaccine efficacy. Substitutions employed during vaccine production using embryonated eggs (i.e., egg passage adaptation) contribute to the poor vaccine efficacy (VE), but the evolutionary mechanism remains elusive. Using an unprecedented number of hemagglutinin sequences (n = 89,853), we found that the fitness landscape of passage adaptation is dominated by pervasive epistasis between two leading residues (186 and 194) and multiple other positions. Convergent evolutionary paths driven by strong epistasis explain most of the variation in VE, which has resulted in extremely poor vaccines for the past decade. Leveraging the unique fitness landscape, we developed a novel machine learning model that can predict egg passage substitutions for any candidate vaccine strain before the passage experiment, providing a unique opportunity for the selection of optimal vaccine viruses. Our study presents one of the most comprehensive characterizations of the fitness landscape of a virus and demonstrates that evolutionary trajectories can be harnessed for improved influenza vaccines. |
format | Online Article Text |
id | pubmed-9501976 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95019762022-09-24 Predicting Egg Passage Adaptations to Design Better Vaccines for the H3N2 Influenza Virus Liu, Yunsong Chen, Hui Duan, Wenyuan Zhang, Xinyi He, Xionglei Nielsen, Rasmus Ma, Liang Zhai, Weiwei Viruses Article Seasonal H3N2 influenza evolves rapidly, leading to an extremely poor vaccine efficacy. Substitutions employed during vaccine production using embryonated eggs (i.e., egg passage adaptation) contribute to the poor vaccine efficacy (VE), but the evolutionary mechanism remains elusive. Using an unprecedented number of hemagglutinin sequences (n = 89,853), we found that the fitness landscape of passage adaptation is dominated by pervasive epistasis between two leading residues (186 and 194) and multiple other positions. Convergent evolutionary paths driven by strong epistasis explain most of the variation in VE, which has resulted in extremely poor vaccines for the past decade. Leveraging the unique fitness landscape, we developed a novel machine learning model that can predict egg passage substitutions for any candidate vaccine strain before the passage experiment, providing a unique opportunity for the selection of optimal vaccine viruses. Our study presents one of the most comprehensive characterizations of the fitness landscape of a virus and demonstrates that evolutionary trajectories can be harnessed for improved influenza vaccines. MDPI 2022-09-17 /pmc/articles/PMC9501976/ /pubmed/36146872 http://dx.doi.org/10.3390/v14092065 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Liu, Yunsong Chen, Hui Duan, Wenyuan Zhang, Xinyi He, Xionglei Nielsen, Rasmus Ma, Liang Zhai, Weiwei Predicting Egg Passage Adaptations to Design Better Vaccines for the H3N2 Influenza Virus |
title | Predicting Egg Passage Adaptations to Design Better Vaccines for the H3N2 Influenza Virus |
title_full | Predicting Egg Passage Adaptations to Design Better Vaccines for the H3N2 Influenza Virus |
title_fullStr | Predicting Egg Passage Adaptations to Design Better Vaccines for the H3N2 Influenza Virus |
title_full_unstemmed | Predicting Egg Passage Adaptations to Design Better Vaccines for the H3N2 Influenza Virus |
title_short | Predicting Egg Passage Adaptations to Design Better Vaccines for the H3N2 Influenza Virus |
title_sort | predicting egg passage adaptations to design better vaccines for the h3n2 influenza virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9501976/ https://www.ncbi.nlm.nih.gov/pubmed/36146872 http://dx.doi.org/10.3390/v14092065 |
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