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Record W4312967855 · doi:10.2196/42700

SARS-CoV-2 Omicron Variant Genomic Sequences and Their Epidemiological Correlates Regarding the End of the Pandemic: In Silico Analysis

2022· article· en· W4312967855 on OpenAlexvenueno aff
Ashutosh Kumar, Adil Asghar, Himanshu Narayan Singh, Muneeb A. Faiq, Sujeet Kumar, Ravi Kant Narayan, Gopichand Kumar, Prakhar Dwivedi, Chetan Sahni, Rakesh Kumar Jha, Maheswari Kulandhasamy, Pranav Prasoon, Kishore Sesham, Kamla Kant, Sada N. Pandey

Bibliographic record

VenueJMIR Bioinformatics and Biotechnology · 2022
Typearticle
Languageen
FieldMedicine
TopicSARS-CoV-2 and COVID-19 Research
Canadian institutionsnot available
Fundersnot available
KeywordsGeneticsIn silicoBiologySequence analysisPandemicSpike ProteinGenomeSingle-nucleotide polymorphismCoronavirus disease 2019 (COVID-19)VirologyComputational biologyGeneMedicineGenotypeInfectious disease (medical specialty)Disease

Abstract

fetched live from OpenAlex

BACKGROUND A newly emerged SARS-CoV-2 variant B.1.1.529 worried the health policy makers worldwide due to a large number of mutations in its genomic sequence, especially in the spike protein region. World Health Organization (WHO) designated it as a global variant of concern (VOC) and was named 'Omicron.' Following Omicron's emergence, a surge in new COVID-19 cases was reported globally, primarily in South Africa (SA). OBJECTIVE We aimed to understand whether the Omicron had an epidemiological advantage over existing variants. METHODS We performed an in silico analysis of the complete genomic sequences of Omicron available on GISAID to analyze the functional impact of the mutations present in this variant on virus-host interactions in terms of viral transmissibility, virulence/lethality, and immune escape. In addition, we performed a correlation analysis of the relative proportion of the genomic sequences of specific SARS-CoV-2 variants (in the period of 01 Oct-29 Nov 2021) with the matched epidemiological data (new COVID-19 cases and deaths) from SA. RESULTS Compared to the current list of global VOCs/VOIs (as per WHO), Omicron bears more sequence variation, specifically in the spike protein and host receptor-binding motif (RBM). Omicron showed the closest nucleotide and protein sequence homology with the Alpha variant for the complete sequence and RBM. The mutations were found primarily condensed in the spike region (28-48) of the virus. Further, the mutational analysis showed enrichment for the mutations decreasing ACE2-binding affinity and RBD protein expression, in contrast, increasing the propensity of immune escape. An inverse correlation of Omicron with Delta variant was noted (r=-0.99, p< .001, 95% CI: -0.99 to -0.97) in the sequences reported from SA post-emergence of the new variant, later showing a decrease. There was a steep rise in the new COVID-19 cases in parallel with the increase in the proportion of Omicron since the first case (74-100%). In contrary, the incidences of new deaths was not increased (r=-0.04, p>0.05, 95% CI =-0.52 to 0.58). CONCLUSIONS In silico analysis of the viral genomic sequences suggest that the Omicron variant has more remarkable immune escape ability than the existing VOCs/VOIs, including Delta, but lesser virulence/lethality than other reported variants. The higher power for immune escape for Omicron was a likely reason for the surge in COVID-19 cases and soon becoming a globally dominant strain. They were more infectious but less lethal than the existing variants, hence outpaced them, thus scripting the pandemic's downfall.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.002
metaresearch head score (Gemma)0.003
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Simulation or modeling · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.003
Threshold uncertainty score0.009

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.003
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.003
Bibliometrics0.0020.002
Science and technology studies0.0010.000
Scholarly communication0.0010.000
Open science0.0010.000
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0020.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.038
GPT teacher head0.317
Teacher spread0.278 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designSimulation or modeling
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations5
Published2022
Admission routes1
Has abstractyes

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