Evidence map›Paper›PMID 34969951›Full record

ArticleScientific reports2021

A global analysis of conservative and non-conservative mutations in SARS-CoV-2 detected in the first year of the COVID-19 world-wide diffusion.

Nicole Balasco, Gianluca Damaggio, Luciana Esposito, Flavia Villani, Rita Berisio, Vincenza Colonna, Luigi Vitagliano

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Structure-Based Development of SARS-CoV-2 Spike Interactors.International journal of molecular sciences · 2022
    Article
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

7 authors at 2 institutions in 1 country.

Nicole Balasco *Institute of Biostructures and Bioimaging, National Research Council (CNR), Naples, Italy.
Gianluca Damaggio *Institute of Genetics and Biophysics, National Research Council (CNR), Naples, Italy.
Luciana EspositoInstitute of Biostructures and Bioimaging, National Research Council (CNR), Naples, Italy.
Flavia VillaniInstitute of Genetics and Biophysics, National Research Council (CNR), Naples, Italy.
Rita BerisioInstitute of Biostructures and Bioimaging, National Research Council (CNR), Naples, Italy.
Vincenza ColonnaInstitute of Genetics and Biophysics, National Research Council (CNR), Naples, Italy.
Luigi VitaglianoInstitute of Biostructures and Bioimaging, National Research Council (CNR), Naples, Italy. luigi.vitagliano@unina.it.
National Research Council · ITInstitute of Genetics and Biophysics · IT

Funding

Regione Campania RicErCa e sviluppO VERsus COVID19 in Campania RECOVER-COVID19
6 · The paper itself

Abstract

The ability of SARS-CoV-2 to rapidly mutate represents a remarkable complicancy. Quantitative evaluations of the effects that these mutations have on the virus structure/function is of great relevance and the availability of a large number of SARS-CoV-2 sequences since the early phases of the pandemic represents a unique opportunity to follow the adaptation of the virus to humans. Here, we evaluated the SARS-CoV-2 amino acid mutations and their progression by analyzing publicly available viral genomes at three stages of the pandemic (2020 March 15th and October 7th, 2021 February 7th). Mutations were classified in conservative and non-conservative based on the probability to be accepted during the evolution according to the Point Accepted Mutation substitution matrices and on the similarity of the encoding codons. We found that the most frequent substitutions are T > I, L > F, and A > V and we observe accumulation of hydrophobic residues. These findings are consistent among the three stages analyzed. We also found that non-conservative mutations are less frequent than conservative ones. This finding may be ascribed to a progressive adaptation of the virus to the host. In conclusion, the present study provides indications of the early evolution of the virus and tools for the global and genome-specific evaluation of the possible impact of mutations on the structure/function of SARS-CoV-2 variants.

Indexed as

Genetic VariationGenome, ViralPandemicsCOVID-19HumansMutationSARS-CoV-2

Identifiers

PMID34969951
PMCPMC8718531
OpenAlexW4200517882

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.