Evidence map›Paper›PMID 36688013›Full record

ArticleJMIR bioinformatics and biotechnology2023

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

Ashutosh Kumar, Adil Asghar, Himanshu N Singh, Muneeb A Faiq, Sujeet Kumar, Ravi K Narayan, Gopichand Kumar, Prakhar Dwivedi, Chetan Sahni, Rakesh K Jha and 5 more

Open access · diamondAbstract read
In one paragraph

Article in JMIR bioinformatics and biotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-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

5 citing papers in PubMed, 5 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

15 authors at 2 institutions in 2 countries.

Ashutosh KumarDepartment of Anatomy All India Institute of Medical Sciences-Patna Patna India.ORCID https://orcid.org/0000-0003-1589-9568
Adil AsgharDepartment of Anatomy All India Institute of Medical Sciences-Patna Patna India.ORCID https://orcid.org/0000-0002-1404-1298
Himanshu N SinghEtiologically Elusive Disorders Research Network New Delhi India.ORCID https://orcid.org/0000-0003-4111-5165
Muneeb A FaiqEtiologically Elusive Disorders Research Network New Delhi India.ORCID https://orcid.org/0000-0002-1430-3139
Sujeet KumarEtiologically Elusive Disorders Research Network New Delhi India.ORCID https://orcid.org/0000-0001-5427-8735
Ravi K NarayanEtiologically Elusive Disorders Research Network New Delhi India.ORCID https://orcid.org/0000-0003-2510-6744
Gopichand KumarDepartment of Anatomy All India Institute of Medical Sciences-Patna Patna India.ORCID https://orcid.org/0000-0002-3100-8908
Prakhar DwivediDepartment of Anatomy All India Institute of Medical Sciences-Patna Patna India.ORCID https://orcid.org/0000-0001-8756-1676
Chetan SahniEtiologically Elusive Disorders Research Network New Delhi India.ORCID https://orcid.org/0000-0002-4301-4643
Rakesh K JhaDepartment of Anatomy All India Institute of Medical Sciences-Patna Patna India.ORCID https://orcid.org/0000-0003-1292-5927
Maheswari KulandhasamyEtiologically Elusive Disorders Research Network New Delhi India.ORCID https://orcid.org/0000-0002-6769-2596
Pranav PrasoonEtiologically Elusive Disorders Research Network New Delhi India.ORCID https://orcid.org/0000-0002-5035-3619
Kishore SeshamEtiologically Elusive Disorders Research Network New Delhi India.ORCID https://orcid.org/0000-0002-6196-5565
Kamla KantEtiologically Elusive Disorders Research Network New Delhi India.ORCID https://orcid.org/0000-0002-8966-6268
Sada N PandeyEtiologically Elusive Disorders Research Network New Delhi India.ORCID https://orcid.org/0000-0003-3201-2287
Global Development Network · INCentral University of Punjab · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Emergence of the new SARS-CoV-2 variant B.1.1.529 worried health policy makers worldwide due to a large number of mutations in its genomic sequence, especially in the spike protein region. The World Health Organization (WHO) designated this variant as a global variant of concern (VOC), which was named "Omicron." Following Omicron's emergence, a surge of new COVID-19 cases was reported globally, primarily in South Africa. Objective: The aim of this study was to understand whether Omicron had an epidemiological advantage over existing variants. Methods: We performed an in silico analysis of the complete genomic sequences of Omicron available on the Global Initiative on Sharing Avian Influenza Data (GISAID) database 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 from October 1 to November 29, 2021) with matched epidemiological data (new COVID-19 cases and deaths) from South Africa. Results: Compared with the current list of global VOCs/variants of interest (VOIs), as per the 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 the RBM. The mutations were found to be primarily condensed in the spike region (n=28-48) of the virus. Further mutational analysis showed enrichment for the mutations decreasing binding affinity to angiotensin-converting enzyme 2 receptor and receptor-binding domain protein expression, and for increasing the propensity of immune escape. An inverse correlation of Omicron with the Delta variant was noted (r=-0.99, Conclusions: In silico analysis of viral genomic sequences suggests that the Omicron variant has more remarkable immune-escape ability than existing VOCs/VOIs, including Delta, but reduced virulence/lethality than other reported variants. The higher power for immune escape for Omicron was a likely reason for the resurgence in COVID-19 cases and its rapid rise as the globally dominant strain. Being more infectious but less lethal than the existing variants, Omicron could have plausibly led to widespread unnoticed new, repeated, and vaccine breakthrough infections, raising the population-level immunity barrier against the emergence of new lethal variants. The Omicron variant could have thus paved the way for the end of the pandemic.

Indexed as

COVID-19dataepidemiologygenomicimmune escapemutationsOmicronpandemicpolicytransmissibilitytransmissionvariantsvirulencevirus

Identifiers

PMID36688013
PMCPMC9843602
OpenAlexW4312967855

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.