Evidence map›Paper›PMID 37896909›Full record

ArticleViruses2023

Emergence of Genomic Diversity in the Spike Protein of the "Omicron" Variant.

Surajit Basak, Pratanu Kayet, Manisha Ghosh, Joyeeta Chatterjee, Shanta Dutta

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
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

5 authors at 2 institutions in 1 country.

Surajit BasakDivision of Bioinformatics, ICMR-National Institute of Cholera and Enteric Diseases, Kolkata 700010, India.ORCID 0000-0002-5199-1022
Pratanu KayetDivision of Bioinformatics, ICMR-National Institute of Cholera and Enteric Diseases, Kolkata 700010, India.
Manisha GhoshDivision of Bioinformatics, ICMR-National Institute of Cholera and Enteric Diseases, Kolkata 700010, India.
Joyeeta ChatterjeeCentre for Bioinformatics, School of Life Sciences, Pondicherry University, Pondicherry 605014, India.ORCID 0009-0009-1705-4922
Shanta DuttaDivision of Bacteriology, ICMR-National Institute of Cholera and Enteric Diseases, Kolkata 700010, India.
National Institute of Cholera and Enteric Diseases · INPondicherry University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus) has constantly been evolving into different forms throughout its spread in the population. Emerging SARS-CoV-2 variants, predominantly the variants of concern (VOCs), could have an impact on the virus spread, pathogenicity, and diagnosis. The recently emerged "Omicron" variant has exhibited rapid transmission and divergence. The spike protein of SARS-CoV-2 has consistently been appearing as the mutational hotspot of all these VOCs. In order to determine a deeper understanding of the recently emerged and extremely divergent "Omicron", a study of amino acid usage patterns and their substitution patterns was performed and compared with those of the other four successful variants of concern ("Alpha", "Beta", "Gamma", and "Delta"). We observed that the amino acid usage of "Omicron" has a distinct pattern that distinguishes it from other VOCs and is significantly correlated with the increased hydrophobicity in spike proteins. We observed an increase in the non-synonymous substitution rate compared with the other four VOCs. Considering the phylogenetic relationship, we hypothesized about the functional interdependence between recombination and the mutation rate that might have resulted in a shift in the optimum of the mutation rate for the evolution of the "Omicron" variant. The results suggest that for improved disease prevention and control, more attention should be given to the significant genetic differentiation and diversity of newly emerging variants.

Indexed as

GenomicsSpike Glycoprotein, CoronavirusAmino AcidsGenetic DriftPhylogenyAmino AcidsSpike Glycoprotein, Coronavirusamino acid usagemutation ratereceptor binding domainrecombinationSARS-CoV-2VOC

Identifiers

PMID37896909
PMCPMC10612054
OpenAlexW4387843684

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.