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Molecular evolutionary analyses of the fusion protein gene in human respirovirus 1
Few evolutionary studies of the human respiratory virus (HRV) have been conducted, but most of them have focused on HRV3. In this study, the full-length fusion (F) genes in HRV1 strains collected from various countries were subjected to time-scaled phylogenetic, genome population size, and selective...
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/PMC10352714/ https://www.ncbi.nlm.nih.gov/pubmed/37270034 http://dx.doi.org/10.1016/j.virusres.2023.199142 |
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author | Takahashi, Tomoko Akagawa, Mao Kimura, Ryusuke Sada, Mitsuru Shirai, Tatsuya Okayama, Kaori Hayashi, Yuriko Kondo, Mayumi Takeda, Makoto Ryo, Akihide Kimura, Hirokazu |
author_facet | Takahashi, Tomoko Akagawa, Mao Kimura, Ryusuke Sada, Mitsuru Shirai, Tatsuya Okayama, Kaori Hayashi, Yuriko Kondo, Mayumi Takeda, Makoto Ryo, Akihide Kimura, Hirokazu |
author_sort | Takahashi, Tomoko |
collection | PubMed |
description | Few evolutionary studies of the human respiratory virus (HRV) have been conducted, but most of them have focused on HRV3. In this study, the full-length fusion (F) genes in HRV1 strains collected from various countries were subjected to time-scaled phylogenetic, genome population size, and selective pressure analyses. Antigenicity analysis was performed on the F protein. The time-scaled phylogenetic tree using the Bayesian Markov Chain Monte Carlo method estimated that the common ancestor of the HRV1 F gene diverged in 1957 and eventually formed three lineages. Phylodynamic analyses showed that the genome population size of the F gene has doubled over approximately 80 years. Phylogenetic distances between the strains were short (< 0.02). No positive selection sites were detected for the F protein, whereas many negative selection sites were identified. Almost all conformational epitopes of the F protein, except one in each monomer, did not correspond to the neutralising antibody (NT-Ab) binding sites. These results suggest that the HRV1 F gene has constantly evolved over many years, infecting humans, while the gene may be relatively conserved. Mismatches between computationally predicted epitopes and NT-Ab binding sites may be partially responsible for HRV1 reinfection and other viruses such as HRV3 and respiratory syncytial virus. |
format | Online Article Text |
id | pubmed-10352714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-103527142023-07-19 Molecular evolutionary analyses of the fusion protein gene in human respirovirus 1 Takahashi, Tomoko Akagawa, Mao Kimura, Ryusuke Sada, Mitsuru Shirai, Tatsuya Okayama, Kaori Hayashi, Yuriko Kondo, Mayumi Takeda, Makoto Ryo, Akihide Kimura, Hirokazu Virus Res Article Few evolutionary studies of the human respiratory virus (HRV) have been conducted, but most of them have focused on HRV3. In this study, the full-length fusion (F) genes in HRV1 strains collected from various countries were subjected to time-scaled phylogenetic, genome population size, and selective pressure analyses. Antigenicity analysis was performed on the F protein. The time-scaled phylogenetic tree using the Bayesian Markov Chain Monte Carlo method estimated that the common ancestor of the HRV1 F gene diverged in 1957 and eventually formed three lineages. Phylodynamic analyses showed that the genome population size of the F gene has doubled over approximately 80 years. Phylogenetic distances between the strains were short (< 0.02). No positive selection sites were detected for the F protein, whereas many negative selection sites were identified. Almost all conformational epitopes of the F protein, except one in each monomer, did not correspond to the neutralising antibody (NT-Ab) binding sites. These results suggest that the HRV1 F gene has constantly evolved over many years, infecting humans, while the gene may be relatively conserved. Mismatches between computationally predicted epitopes and NT-Ab binding sites may be partially responsible for HRV1 reinfection and other viruses such as HRV3 and respiratory syncytial virus. Elsevier 2023-06-09 /pmc/articles/PMC10352714/ /pubmed/37270034 http://dx.doi.org/10.1016/j.virusres.2023.199142 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 Takahashi, Tomoko Akagawa, Mao Kimura, Ryusuke Sada, Mitsuru Shirai, Tatsuya Okayama, Kaori Hayashi, Yuriko Kondo, Mayumi Takeda, Makoto Ryo, Akihide Kimura, Hirokazu Molecular evolutionary analyses of the fusion protein gene in human respirovirus 1 |
title | Molecular evolutionary analyses of the fusion protein gene in human respirovirus 1 |
title_full | Molecular evolutionary analyses of the fusion protein gene in human respirovirus 1 |
title_fullStr | Molecular evolutionary analyses of the fusion protein gene in human respirovirus 1 |
title_full_unstemmed | Molecular evolutionary analyses of the fusion protein gene in human respirovirus 1 |
title_short | Molecular evolutionary analyses of the fusion protein gene in human respirovirus 1 |
title_sort | molecular evolutionary analyses of the fusion protein gene in human respirovirus 1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10352714/ https://www.ncbi.nlm.nih.gov/pubmed/37270034 http://dx.doi.org/10.1016/j.virusres.2023.199142 |
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