Evidence map›Paper›PMID 35071267›Full record

ArticleFrontiers in medicine2021

Genome Sequencing Reveals a Mixed Picture of SARS-CoV-2 Variant of Concern Circulation in Eastern Uttar Pradesh, India.

Hirawati Deval, Dimpal A Nyayanit, Shailendra Kumar Mishra, Pragya D Yadav, Kamran Zaman, Prem Shankar, Brij R Misra, Sthita Pragnya Behera, Niraj Kumar, Abhinendra Kumar and 13 more

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Article in Frontiers in medicine, 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
1.0field-weighted citation impact, top 24% 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, 10 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

23 authors at 4 institutions in 1 country.

Hirawati DevalIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Dimpal A NyayanitIndian Council of Medical Research (ICMR)-National Institute of Virology, Pune, India.
Shailendra Kumar MishraIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Pragya D YadavIndian Council of Medical Research (ICMR)-National Institute of Virology, Pune, India.
Kamran ZamanIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Prem ShankarAll India Institute of Medical Sciences, Gorakhpur, India.
Brij R MisraIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Sthita Pragnya BeheraIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Niraj KumarIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Abhinendra KumarIndian Council of Medical Research (ICMR)-National Institute of Virology, Pune, India.
Pooja BhardwajIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Gaurav Raj DwivediIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Rajeev SinghIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Anita M SheteIndian Council of Medical Research (ICMR)-National Institute of Virology, Pune, India.
Priyanka PanditIndian Council of Medical Research (ICMR)-National Institute of Virology, Pune, India.
Ashok K PandeyIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Girijesh Kumar YadavIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Shashi GuptaIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Manoj KumarIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Asif KavathekarIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Ravi Shankar SinghIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Sanjay PrajapatiIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Rajni KantIndian Council of Medical Research (ICMR)-Regional Medical Research Centre, Gorakhpur, India.
Indian Council of Medical Research · INRegional Medical Research Centre · INICMR-National Institute of Virology · INAll India Institute of Medical Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Uttar Pradesh is the densely populated state of India and is the sixth highest COVID-19 affected state with 22,904 deaths recorded on November 12, 2021. Whole-genome sequencing (WGS) is being used as a potential approach to investigate genomic evolution of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus. In this study, a total of 87 SARS-CoV-2 genomes-49 genomes from the first wave (March 2020 to February 2021) and 38 genomes from the second wave (March 2021 to July 2021) from Eastern Uttar Pradesh (E-UP) were sequenced and analyzed to understand its evolutionary pattern and variants against publicaly available sequences. The complete genome analysis of SARS-CoV-2 during the first wave in E-UP largely reported transmission of G, GR, and GH clades with specific mutations. In contrast, variants of concerns (VOCs) such as Delta (71.0%) followed by Delta AY.1 (21.05%) and Kappa (7.9%) lineages belong to G clade with prominent signature amino acids were introduced in the second wave. Signature substitution at positions S:L452R, S:P681R, and S:D614G were commonly detected in the Delta, Delta AY.1, and Kappa variants whereas S:T19R and S:T478K were confined to Delta and Delta AY.1 variants only. Vaccine breakthrough infections showed unique mutational changes at position S:D574Y in the case of the Delta variant, whereas position S:T95 was conserved among Kappa variants compared to the Wuhan isolate. During the transition from the first to second waves, a shift in the predominant clade from GH to G clade was observed. The identified spike protein mutations in the SARS-CoV-2 genome could be used as the potential target for vaccine and drug development to combat the effects of the COVID-19 disease.

Indexed as

COVID-19 breakthrough infectionEastern Uttar Pradesh IndiamutationsSARS-CoV-2variant of concernwhole-genome sequencing

Identifiers

PMID35071267
PMCPMC8777020
OpenAlexW4206307850

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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.