Evidence map›Paper›PMID 32814791›Full record

ArticleScientific reports2020

Genome-wide analysis of SARS-CoV-2 virus strains circulating worldwide implicates heterogeneity.

M Rafiul Islam, M Nazmul Hoque, M Shaminur Rahman, A S M Rubayet Ul Alam, Masuda Akther, J Akter Puspo, Salma Akter, Munawar Sultana, Keith A Crandall, M Anwar Hossain

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 168 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
168citing papers in PubMed, 3 pooled it
7.1field-weighted citation impact, top 2% 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

168 citing papers in PubMed, 3 syntheses or guidelines pooled it, 294 citations in OpenAlex.

  1. COVID-19 pandemic: the delta variant, T-cell responses, and the efficacy of developing vaccines.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
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  9. Detection of SARS-CoV-2 variants in hospital wastewater in Peru, 2022.Revista peruana de medicina experimental y salud publica · 2024
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  14. Human Challenge Studies with Coronaviruses Old and New.Current topics in microbiology and immunology · 2024
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108 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

M Rafiul Islam *Department of Microbiology, University of Dhaka, Dhaka, 1000, Bangladesh.
M Nazmul Hoque *Department of Microbiology, University of Dhaka, Dhaka, 1000, Bangladesh.
M Shaminur Rahman *Department of Microbiology, University of Dhaka, Dhaka, 1000, Bangladesh.
A S M Rubayet Ul AlamDepartment of Microbiology, Jashore University of Science and Technology, Jashore, 7408, Bangladesh.
Masuda AktherDepartment of Microbiology, University of Dhaka, Dhaka, 1000, Bangladesh.
J Akter PuspoDepartment of Microbiology, University of Dhaka, Dhaka, 1000, Bangladesh.
Salma AkterDepartment of Microbiology, University of Dhaka, Dhaka, 1000, Bangladesh.
Munawar SultanaDepartment of Microbiology, University of Dhaka, Dhaka, 1000, Bangladesh.
Keith A CrandallComputational Biology Institute, Milken Institute School of Public Health, The George Washington University, Washington, USA.
M Anwar HossainDepartment of Microbiology, University of Dhaka, Dhaka, 1000, Bangladesh. hossaina@du.ac.bd.
University of Dhaka · BDBangabandhu Sheikh Mujibur Rahman Agricultural University · BDMilken Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), a novel evolutionary divergent RNA virus, is responsible for the present devastating COVID-19 pandemic. To explore the genomic signatures, we comprehensively analyzed 2,492 complete and/or near-complete genome sequences of SARS-CoV-2 strains reported from across the globe to the GISAID database up to 30 March 2020. Genome-wide annotations revealed 1,516 nucleotide-level variations at different positions throughout the entire genome of SARS-CoV-2. Moreover, nucleotide (nt) deletion analysis found twelve deletion sites throughout the genome other than previously reported deletions at coding sequence of the ORF8 (open reading frame), spike, and ORF7a proteins, specifically in polyprotein ORF1ab (n = 9), ORF10 (n = 1), and 3´-UTR (n = 2). Evidence from the systematic gene-level mutational and protein profile analyses revealed a large number of amino acid (aa) substitutions (n = 744), demonstrating the viral proteins heterogeneous. Notably, residues of receptor-binding domain (RBD) showing crucial interactions with angiotensin-converting enzyme 2 (ACE2) and cross-reacting neutralizing antibody were found to be conserved among the analyzed virus strains, except for replacement of lysine with arginine at 378th position of the cryptic epitope of a Shanghai isolate, hCoV-19/Shanghai/SH0007/2020 (EPI_ISL_416320). Furthermore, our results of the preliminary epidemiological data on SARS-CoV-2 infections revealed that frequency of aa mutations were relatively higher in the SARS-CoV-2 genome sequences of Europe (43.07%) followed by Asia (38.09%), and North America (29.64%) while case fatality rates remained higher in the European temperate countries, such as Italy, Spain, Netherlands, France, England and Belgium. Thus, the present method of genome annotation employed at this early pandemic stage could be a promising tool for monitoring and tracking the continuously evolving pandemic situation, the associated genetic variants, and their implications for the development of effective control and prophylaxis strategies.

Indexed as

Genetic HeterogeneityGlobal HealthAmino Acid SequenceAngiotensin-Converting Enzyme 2Antibodies, NeutralizingBase Pair MismatchBase SequenceBetacoronavirusClimateCoronavirus InfectionsCOVID-19Genome, ViralGenome-Wide Association StudyHumansOpen Reading FramesPandemicsACE2 protein, humanAngiotensin-Converting Enzyme 2Antibodies, NeutralizingPeptidyl-Dipeptidase ASpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID32814791
PMCPMC7438523
OpenAlexW3067557104

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.