Evidence map›Paper›PMID 32970329›Full record

ArticleJournal of medical virology2021

Genomic and proteomic mutation landscapes of SARS-CoV-2.

Christian Luke D C Badua, Karol Ann T Baldo, Paul Mark B Medina

Open access · bronzeAbstract read
In one paragraph

Article in Journal of medical virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 7% 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

55 citing papers in PubMed, 2 syntheses or guidelines pooled it, 111 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

3 authors at 1 institution in 1 country.

Christian Luke D C BaduaDepartment of Biochemistry and Molecular Biology, Biological Models Laboratory, University of the Philippines Manila, Ermita, Manila, Philippines.ORCID 0000-0002-1114-1322
Karol Ann T BaldoDepartment of Biochemistry and Molecular Biology, Biological Models Laboratory, University of the Philippines Manila, Ermita, Manila, Philippines.ORCID 0000-0001-7854-7004
Paul Mark B MedinaDepartment of Biochemistry and Molecular Biology, Biological Models Laboratory, University of the Philippines Manila, Ermita, Manila, Philippines.ORCID 0000-0001-6116-1818
University of the Philippines Manila · PH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ongoing pandemic caused by a novel coronavirus, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), affects thousands of people every day worldwide. Hence, drugs and vaccines effective against all variants of SARS-CoV-2 are crucial today. Viral genome mutations exist commonly which may impact the encoded proteins, possibly resulting to varied effectivity of detection tools and disease treatment. Thus, this study surveyed the SARS-CoV-2 genome and proteome and evaluated its mutation characteristics. Phylogenetic analyses of SARS-CoV-2 genes and proteins show three major clades and one minor clade (P6810S; ORF1ab). The overall frequency and densities of mutations in the genes and proteins of SARS-CoV-2 were observed. Nucleocapsid exhibited the highest mutation density among the structural proteins while the spike D614G was the most common, occurring mostly in genomes outside China and United States. ORF8 protein had the highest mutation density across all geographical areas. Moreover, mutation hotspots neighboring and at the catalytic site of RNA-dependent RNA polymerase were found that might challenge the binding and effectivity of remdesivir. Mutation coldspots may present as conserved diagnostic and therapeutic targets were found in ORF7b, ORF9b, and ORF14. These findings suggest that the virion's genotype and phenotype in a specific population should be considered in developing diagnostic tools and treatment options.

Indexed as

Genome, ViralMutationPhylogenyProteomeChinaCOVID-19Evolution, MolecularGenomicsHumansOpen Reading FramesProteomicsSARS-CoV-2Spike Glycoprotein, CoronavirusUnited StatesViral ProteinsORF7b protein, SARS-CoV-2ORF8 protein, SARS-CoV-2ProteomeSpike Glycoprotein, CoronavirusViral Proteinscoldspotcoronavirusgenetic variabilitymutationmutation hotspotSARS-CoV-2virus bioinformatics

Identifiers

PMID32970329
PMCPMC7537117
OpenAlexW3088334807

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.