Evidence map›Paper›PMID 35371557›Full record

ArticleVirus evolution2022

Large-scale analysis of SARS-CoV-2 synonymous mutations reveals the adaptation to the human codon usage during the virus evolution.

Daniele Ramazzotti, Fabrizio Angaroni, Davide Maspero, Mario Mauri, Deborah D'Aliberti, Diletta Fontana, Marco Antoniotti, Elena Maria Elli, Alex Graudenzi, Rocco Piazza

Open access · goldAbstract read
In one paragraph

Article in Virus evolution, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
7.3field-weighted citation impact, top 2% of its field
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

25 citing papers in PubMed, 63 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Fabrizio AngaroniDepartment of Informatics, Systems and Communication, Università degli Studi di Milano-Bicocca, Viale Sarca 336, Milano 20100, Italy.
Davide MasperoDepartment of Informatics, Systems and Communication, Università degli Studi di Milano-Bicocca, Viale Sarca 336, Milano 20100, Italy.
Mario MauriDepartment of Medicine and Surgery, Università degli Studi di Milano-Bicocca, Via Cadore 48, Monza 20900, Italy.
Deborah D'AlibertiDepartment of Medicine and Surgery, Università degli Studi di Milano-Bicocca, Via Cadore 48, Monza 20900, Italy.
Diletta FontanaDepartment of Medicine and Surgery, Università degli Studi di Milano-Bicocca, Via Cadore 48, Monza 20900, Italy.ORCID https://orcid.org/0000-0003-1633-6310
Marco AntoniottiDepartment of Informatics, Systems and Communication, Università degli Studi di Milano-Bicocca, Viale Sarca 336, Milano 20100, Italy.
Elena Maria ElliDepartment of Medicine and Surgery, Università degli Studi di Milano-Bicocca, Via Cadore 48, Monza 20900, Italy.
Alex GraudenziInstitution of Molecular Bioimaging and Physiology, Consiglio Nazionale delle Ricerche (IBFM-CNR), Via fratelli Cervi 93, Segrate 20054, Italy.
Rocco PiazzaDepartment of Medicine and Surgery, Università degli Studi di Milano-Bicocca, Via Cadore 48, Monza 20900, Italy.
University of Milano-Bicocca · ITInstitute of Molecular Bioimaging and Physiology · ITAzienda Ospedaliera San Gerardo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many large national and transnational studies have been dedicated to the analysis of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) genome, most of which focused on missense and nonsense mutations. However, approximately 30 per cent of the SARS-CoV-2 variants are synonymous, therefore changing the target codon without affecting the corresponding protein sequence. By performing a large-scale analysis of sequencing data generated from almost 400,000 SARS-CoV-2 samples, we show that silent mutations increasing the similarity of viral codons to the human ones tend to fixate in the viral genome overtime. This indicates that SARS-CoV-2 codon usage is adapting to the human host, likely improving its effectiveness in using the human aminoacyl-tRNA set through the accumulation of deceitfully neutral silent mutations. One-Sentence Summary. Synonymous SARS-CoV-2 mutations related to the activity of different mutational processes may positively impact viral evolution by increasing its adaptation to the human codon usage.

Indexed as

codon usageintra-host variantsSARS-CoV-2viral adaptationviral genomics

Identifiers

PMID35371557
PMCPMC8971538
OpenAlexW4221085637

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.