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Antigenicity prediction and vaccine recommendation of human influenza virus A (H3N2) using convolutional neural networks

The rapid evolution of influenza A viruses poses a great challenge to vaccine development. Analytical and machine learning models have been applied to facilitate the process of antigenicity determination. In this study, we designed deep convolutional neural networks (CNNs) to predict Influenza antig...

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Autores principales: Lee, Eva K., Tian, Haozheng, Nakaya, Helder I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734114/
https://www.ncbi.nlm.nih.gov/pubmed/32750260
http://dx.doi.org/10.1080/21645515.2020.1734397
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author Lee, Eva K.
Tian, Haozheng
Nakaya, Helder I.
author_facet Lee, Eva K.
Tian, Haozheng
Nakaya, Helder I.
author_sort Lee, Eva K.
collection PubMed
description The rapid evolution of influenza A viruses poses a great challenge to vaccine development. Analytical and machine learning models have been applied to facilitate the process of antigenicity determination. In this study, we designed deep convolutional neural networks (CNNs) to predict Influenza antigenicity. Our model is the first that systematically analyzed 566 amino acid properties and 141 amino acid substitution matrices for their predictability. We then optimized the structure of the CNNs using particle swarm optimization. The optimal neural networks outperform other predictive models with a blind validation accuracy of 95.8%. Further, we applied our model to vaccine recommendations in the period 1997 to 2011 and contrasted the performance of previous vaccine recommendations using traditional experimental approaches. The results show that our model outperforms the WHO recommendation and other existing models and could potentially improve the vaccine recommendation process. Our results show that WHO often selects virus strains with small variation from year to year and learns slowly and recovers once coverage dips very low. In contrast, the influenza strains selected via our CNN model can differ quite drastically from year to year and exhibit consistently good coverage. In summary, we have designed a comprehensive computational pipeline for optimizing a CNN in the modeling of Influenza A antigenicity and vaccine recommendation. It is more cost and time-effective when compared to traditional hemagglutination inhibition assay analysis. The modeling framework is flexible and can be adopted to study other type of viruses.
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spelling pubmed-77341142020-12-18 Antigenicity prediction and vaccine recommendation of human influenza virus A (H3N2) using convolutional neural networks Lee, Eva K. Tian, Haozheng Nakaya, Helder I. Hum Vaccin Immunother Research Paper The rapid evolution of influenza A viruses poses a great challenge to vaccine development. Analytical and machine learning models have been applied to facilitate the process of antigenicity determination. In this study, we designed deep convolutional neural networks (CNNs) to predict Influenza antigenicity. Our model is the first that systematically analyzed 566 amino acid properties and 141 amino acid substitution matrices for their predictability. We then optimized the structure of the CNNs using particle swarm optimization. The optimal neural networks outperform other predictive models with a blind validation accuracy of 95.8%. Further, we applied our model to vaccine recommendations in the period 1997 to 2011 and contrasted the performance of previous vaccine recommendations using traditional experimental approaches. The results show that our model outperforms the WHO recommendation and other existing models and could potentially improve the vaccine recommendation process. Our results show that WHO often selects virus strains with small variation from year to year and learns slowly and recovers once coverage dips very low. In contrast, the influenza strains selected via our CNN model can differ quite drastically from year to year and exhibit consistently good coverage. In summary, we have designed a comprehensive computational pipeline for optimizing a CNN in the modeling of Influenza A antigenicity and vaccine recommendation. It is more cost and time-effective when compared to traditional hemagglutination inhibition assay analysis. The modeling framework is flexible and can be adopted to study other type of viruses. Taylor & Francis 2020-08-04 /pmc/articles/PMC7734114/ /pubmed/32750260 http://dx.doi.org/10.1080/21645515.2020.1734397 Text en © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Paper
Lee, Eva K.
Tian, Haozheng
Nakaya, Helder I.
Antigenicity prediction and vaccine recommendation of human influenza virus A (H3N2) using convolutional neural networks
title Antigenicity prediction and vaccine recommendation of human influenza virus A (H3N2) using convolutional neural networks
title_full Antigenicity prediction and vaccine recommendation of human influenza virus A (H3N2) using convolutional neural networks
title_fullStr Antigenicity prediction and vaccine recommendation of human influenza virus A (H3N2) using convolutional neural networks
title_full_unstemmed Antigenicity prediction and vaccine recommendation of human influenza virus A (H3N2) using convolutional neural networks
title_short Antigenicity prediction and vaccine recommendation of human influenza virus A (H3N2) using convolutional neural networks
title_sort antigenicity prediction and vaccine recommendation of human influenza virus a (h3n2) using convolutional neural networks
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734114/
https://www.ncbi.nlm.nih.gov/pubmed/32750260
http://dx.doi.org/10.1080/21645515.2020.1734397
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