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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...

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Autores principales: Takahashi, Tomoko, Akagawa, Mao, Kimura, Ryusuke, Sada, Mitsuru, Shirai, Tatsuya, Okayama, Kaori, Hayashi, Yuriko, Kondo, Mayumi, Takeda, Makoto, Ryo, Akihide, Kimura, Hirokazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
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.
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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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