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Molecular characterization of SARS-CoV-2 detected in Tokyo, Japan during five waves: Identification of the amino acid substitutions associated with transmissibility and severity
Many variants of SARS-CoV-2 have emerged around the world. It is therefore important to understand its global viral evolution and the corresponding mutations associated with transmissibility and severity. In this study, we analyzed 112 whole genome sequences of SARS-CoV-2 collected from patients at...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9363898/ https://www.ncbi.nlm.nih.gov/pubmed/35966679 http://dx.doi.org/10.3389/fmicb.2022.912061 |
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author | Tsuchiya, Koji Yamamoto, Norio Hosaka, Yoshie Wakita, Mitsuru Hiki, Makoto Matsushita, Yasushi Mori, Hirotake Hori, Satoshi Misawa, Shigeki Miida, Takashi Nojiri, Shuko Takahashi, Kazuhisa Naito, Toshio Tabe, Yoko |
author_facet | Tsuchiya, Koji Yamamoto, Norio Hosaka, Yoshie Wakita, Mitsuru Hiki, Makoto Matsushita, Yasushi Mori, Hirotake Hori, Satoshi Misawa, Shigeki Miida, Takashi Nojiri, Shuko Takahashi, Kazuhisa Naito, Toshio Tabe, Yoko |
author_sort | Tsuchiya, Koji |
collection | PubMed |
description | Many variants of SARS-CoV-2 have emerged around the world. It is therefore important to understand its global viral evolution and the corresponding mutations associated with transmissibility and severity. In this study, we analyzed 112 whole genome sequences of SARS-CoV-2 collected from patients at Juntendo University Hospital in Tokyo and the genome data from entire Japan deposited in Global Initiative on Sharing Avian Influenza Data (GISAID) to examine the relationship of amino acid changes with the transmissibility and the severity of each strain/lineage. We identified 12 lineages, including B.1.1.284, B.1.1.214, R.1, AY.29, and AY.29.1, which were prevalent specifically in Japan. B.1.1.284 was most frequently detected in the second wave, but B.1.1.214 became the predominant lineage in the third wave, indicating that B.1.1.214 has a higher transmissibility than B.1.1.284. The most prevalent lineage during the fourth and fifth wave was B.1.1.7 and AY.29, respectively. In regard to the severity of identified lineages, B.1.1.214 was significantly lower than the reference lineage, B.1.1.284. Analysis of the genome sequence and other traits of each lineage/strain revealed the mutations in S, N, and NSPs that increase the transmissibility and/or severity. These mutations include S: M153T, N: P151L, NSP3: S543P, NSP5: P108S, and NSP12: A423V in B.1.1.284; S: W152L and E484K in R.1; S: H69del, V70del, and N501Y in the Alpha strain; S: L452R, T478K, and P681R in the Delta strain. Furthermore, it is suggested that the transmissibility of B.1.1.214 could be enhanced by the mutations N: M234I, NSP14: P43L, and NSP16: R287I. To address the issue of the virus evolution, it is necessary to continuously monitor the genomes of SARS-CoV-2 and analyze the effects of mutations for developing vaccines and antiviral drugs effective against SARS-CoV-2 variants. |
format | Online Article Text |
id | pubmed-9363898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93638982022-08-11 Molecular characterization of SARS-CoV-2 detected in Tokyo, Japan during five waves: Identification of the amino acid substitutions associated with transmissibility and severity Tsuchiya, Koji Yamamoto, Norio Hosaka, Yoshie Wakita, Mitsuru Hiki, Makoto Matsushita, Yasushi Mori, Hirotake Hori, Satoshi Misawa, Shigeki Miida, Takashi Nojiri, Shuko Takahashi, Kazuhisa Naito, Toshio Tabe, Yoko Front Microbiol Microbiology Many variants of SARS-CoV-2 have emerged around the world. It is therefore important to understand its global viral evolution and the corresponding mutations associated with transmissibility and severity. In this study, we analyzed 112 whole genome sequences of SARS-CoV-2 collected from patients at Juntendo University Hospital in Tokyo and the genome data from entire Japan deposited in Global Initiative on Sharing Avian Influenza Data (GISAID) to examine the relationship of amino acid changes with the transmissibility and the severity of each strain/lineage. We identified 12 lineages, including B.1.1.284, B.1.1.214, R.1, AY.29, and AY.29.1, which were prevalent specifically in Japan. B.1.1.284 was most frequently detected in the second wave, but B.1.1.214 became the predominant lineage in the third wave, indicating that B.1.1.214 has a higher transmissibility than B.1.1.284. The most prevalent lineage during the fourth and fifth wave was B.1.1.7 and AY.29, respectively. In regard to the severity of identified lineages, B.1.1.214 was significantly lower than the reference lineage, B.1.1.284. Analysis of the genome sequence and other traits of each lineage/strain revealed the mutations in S, N, and NSPs that increase the transmissibility and/or severity. These mutations include S: M153T, N: P151L, NSP3: S543P, NSP5: P108S, and NSP12: A423V in B.1.1.284; S: W152L and E484K in R.1; S: H69del, V70del, and N501Y in the Alpha strain; S: L452R, T478K, and P681R in the Delta strain. Furthermore, it is suggested that the transmissibility of B.1.1.214 could be enhanced by the mutations N: M234I, NSP14: P43L, and NSP16: R287I. To address the issue of the virus evolution, it is necessary to continuously monitor the genomes of SARS-CoV-2 and analyze the effects of mutations for developing vaccines and antiviral drugs effective against SARS-CoV-2 variants. Frontiers Media S.A. 2022-07-27 /pmc/articles/PMC9363898/ /pubmed/35966679 http://dx.doi.org/10.3389/fmicb.2022.912061 Text en Copyright © 2022 Tsuchiya, Yamamoto, Hosaka, Wakita, Hiki, Matsushita, Mori, Hori, Misawa, Miida, Nojiri, Takahashi, Naito and Tabe. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Tsuchiya, Koji Yamamoto, Norio Hosaka, Yoshie Wakita, Mitsuru Hiki, Makoto Matsushita, Yasushi Mori, Hirotake Hori, Satoshi Misawa, Shigeki Miida, Takashi Nojiri, Shuko Takahashi, Kazuhisa Naito, Toshio Tabe, Yoko Molecular characterization of SARS-CoV-2 detected in Tokyo, Japan during five waves: Identification of the amino acid substitutions associated with transmissibility and severity |
title | Molecular characterization of SARS-CoV-2 detected in Tokyo, Japan during five waves: Identification of the amino acid substitutions associated with transmissibility and severity |
title_full | Molecular characterization of SARS-CoV-2 detected in Tokyo, Japan during five waves: Identification of the amino acid substitutions associated with transmissibility and severity |
title_fullStr | Molecular characterization of SARS-CoV-2 detected in Tokyo, Japan during five waves: Identification of the amino acid substitutions associated with transmissibility and severity |
title_full_unstemmed | Molecular characterization of SARS-CoV-2 detected in Tokyo, Japan during five waves: Identification of the amino acid substitutions associated with transmissibility and severity |
title_short | Molecular characterization of SARS-CoV-2 detected in Tokyo, Japan during five waves: Identification of the amino acid substitutions associated with transmissibility and severity |
title_sort | molecular characterization of sars-cov-2 detected in tokyo, japan during five waves: identification of the amino acid substitutions associated with transmissibility and severity |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9363898/ https://www.ncbi.nlm.nih.gov/pubmed/35966679 http://dx.doi.org/10.3389/fmicb.2022.912061 |
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