Evidence map›Paper›PMID 35266305›Full record

ArticleTransboundary and emerging diseases2022

SARS-CoV-2 variants and spike mutations involved in second wave of COVID-19 pandemic in India.

Radhakrishna Muttineni, Binitha R N, Kalyani Putty, Kavitha Marapakala, Sandra K P, Jaslin Panyam, Aravind Vemula, Shashi Mohan Singh, Subin Balachandran, Viroji Rao S T and 1 more

Open access · greenAbstract read
In one paragraph

Article in Transboundary and emerging diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 15 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

11 authors at 4 institutions in 1 country.

Radhakrishna MuttineniVirus Research Lab, Department of Zoology, Osmania University, Hyderabad, Telangana, India.
Binitha R NDepartment of Zoology, Mar Athanasius College (Autonomous), Kothamangalam, Kerala, India.
Kalyani PuttyDepartment of Veterinary Biotechnology, PVNR Telangana Veterinary University, Hyderabad, Telangana, India.
Kavitha MarapakalaDepartment of Chemistry, University College of Science, Osmania University, Hyderabad, Telangana, India.
Sandra K PDepartment of Biotechnology and Bioinformatics, School of Life Sciences, University of Hyderabad, Telangana, India.
Jaslin PanyamVirus Research Lab, Department of Zoology, Osmania University, Hyderabad, Telangana, India.
Aravind VemulaVirus Research Lab, Department of Zoology, Osmania University, Hyderabad, Telangana, India.
Shashi Mohan SinghVirus Research Lab, Department of Zoology, Osmania University, Hyderabad, Telangana, India.
Subin BalachandranDepartment of Zoology, Mar Athanasius College (Autonomous), Kothamangalam, Kerala, India.
Viroji Rao S TDepartment of Animal Genetics and Breeding, PVNR Telangana Veterinary University, Hyderabad, Telangana, India.
Anand Kumar KondapiDepartment of Biotechnology and Bioinformatics, School of Life Sciences, University of Hyderabad, Telangana, India.
Osmania University · INP.V. Narsimha Rao Telangana Veterinary University · INSacred Heart College · INUniversity of Hyderabad · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Against the backdrop of the second wave of COVID-19 pandemic in India that started in March 2021, we have monitored the spike (S) protein mutations in all the reported (GISAID portal) whole-genome sequences of SARS-CoV-2 circulating in India from 1 January 2021 to 31 August 2021. In the 43,102 SARS-CoV-2 genomic sequences analysed, we have identified 24,260 amino acid mutations in the S protein, based on which 265 Pango lineages could be categorized. The dominant lineage in most of the 28 states of India and its 8 union territories was B.1.617.2 (the delta variant). However, the states Madhya Pradesh, Jammu & Kashmir, and Punjab had B.1.1.7 (alpha variant) as the major lineage, while the Himachal Pradesh state reported B.1.36 as the dominating lineage. A detailed analysis of various domains of S protein was carried out for detecting mutations having a prevalence of >1%; 70, 18, 7, 3, 9, 4, and 1 (N = 112) such mutations were observed in the N-terminal domain, receptor binding domain, C -terminal domain, fusion peptide region, heptapeptide repeat (HR)-1 domains, signal peptide domain, and transmembrane region, respectively. However, no mutations were recorded in the HR-2 and cytoplasmic domains of the S protein. Interestingly, 13.39% (N = 15) of these mutations were reported to increase the infectivity and pathogenicity of the virus; 2% (N = 3) were known to be vaccine breakthrough mutations, and 0.89% (N = 1) were known to escape neutralizing antibodies. The biological significance of 82% (N = 92) of the reported mutations is yet unknown. As SARS-CoV-2 variants are emerging rapidly, it is critical to continuously monitor local viral mutations to understand national trends of virus circulation. This can tremendously help in designing better preventive regimens in the country, and avoid vaccine breakthrough infections.

Indexed as

COVID-19SARS-CoV-2Amino AcidsAnimalsAntibodies, NeutralizingPandemicsPeptidesSpike Glycoprotein, CoronavirusAmino AcidsAntibodies, NeutralizingPeptidesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2B.1.617.2COVID-19 second waveIndiaSARS-CoV-2spike protein variantswhole-genome

Identifiers

PMID35266305
PMCPMC9115369
OpenAlexW4220881631

What OpenQuestion holds

Textmetadata
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.