Evidence map›Paper›PMID 35966679›Full record

ArticleFrontiers in microbiology2022

Molecular characterization of SARS-CoV-2 detected in Tokyo, Japan during five waves: Identification of the amino acid substitutions associated with transmissibility and severity.

Koji Tsuchiya, Norio Yamamoto, Yoshie Hosaka, Mitsuru Wakita, Makoto Hiki, Yasushi Matsushita, Hirotake Mori, Satoshi Hori, Shigeki Misawa, Takashi Miida and 4 more

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Koji TsuchiyaDepartment of Clinical Laboratory, Juntendo University Hospital, Bunkyo, Tokyo, Japan.
Norio YamamotoDepartment of General Medicine, Juntendo University Graduate School of Medicine, Bunkyo-ku, Japan.
Yoshie HosakaDepartment of Clinical Laboratory, Juntendo University Hospital, Bunkyo, Tokyo, Japan.
Mitsuru WakitaDepartment of Clinical Laboratory, Juntendo University Hospital, Bunkyo, Tokyo, Japan.
Makoto HikiDepartment of Emergency Medicine, Juntendo University Faculty of Medicine, Bunkyo-ku, Japan.
Yasushi MatsushitaDepartment of Internal Medicine and Rheumatology, Juntendo University Graduate School of Medicine, Bunkyo-ku, Japan.
Hirotake MoriDepartment of General Medicine, Juntendo University Graduate School of Medicine, Bunkyo-ku, Japan.
Satoshi HoriDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Bunkyo-ku, Japan.
Shigeki MisawaDepartment of Clinical Laboratory, Juntendo University Hospital, Bunkyo, Tokyo, Japan.
Takashi MiidaDepartment of Clinical Laboratory Medicine, Juntendo University Faculty of Medicine, Bunkyo-ku, Japan.
Shuko NojiriMedical Technology Innovation Center, Juntendo University, Bunkyo-ku, Japan.
Kazuhisa TakahashiDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Bunkyo-ku, Japan.
Toshio NaitoDepartment of General Medicine, Juntendo University Graduate School of Medicine, Bunkyo-ku, Japan.
Yoko TabeDepartment of Clinical Laboratory Medicine, Juntendo University Faculty of Medicine, Bunkyo-ku, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

COVID-19genome sequencingJapanSARS-CoV-2severitytransmissibility

Identifiers

PMID35966679
PMCPMC9363898

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.