Evidence map›Paper›PMID 33667722›Full record

ArticleInfection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases2021

Different selection dynamics of S and RdRp between SARS-CoV-2 genomes with and without the dominant mutations.

Necla Koçhan, Doğa Eskier, Aslı Suner, Gökhan Karakülah, Yavuz Oktay

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In one paragraph

Article in Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.3field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 18 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

5 authors at 3 institutions in 1 country.

Necla KoçhanIzmir Biomedicine and Genome Center (IBG), Izmir, Turkey.
Doğa EskierIzmir Biomedicine and Genome Center (IBG), Izmir, Turkey; Izmir International Biomedicine and Genome Institute (iBG-Izmir), Dokuz Eylül University, Izmir, Turkey.
Aslı SunerDepartment of Biostatistics and Medical Informatics, Faculty of Medicine, Ege University, Izmir, Turkey.
Gökhan KarakülahIzmir Biomedicine and Genome Center (IBG), Izmir, Turkey; Izmir International Biomedicine and Genome Institute (iBG-Izmir), Dokuz Eylül University, Izmir, Turkey. Electronic address: gokhan.karakulah@deu.edu.tr.
Yavuz OktayIzmir Biomedicine and Genome Center (IBG), Izmir, Turkey; Izmir International Biomedicine and Genome Institute (iBG-Izmir), Dokuz Eylül University, Izmir, Turkey; Department of Medical Biology, Faculty of Medicine, Dokuz Eylül University, Izmir, Turkey. Electronic address: yavuz.oktay@ibg.edu.tr.
Dokuz Eylül University · TRIzmir University · TREge University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SARS-CoV-2 is a betacoronavirus responsible for the COVID-19 pandemic that has affected millions of people worldwide. Pharmaceutical research against COVID-19 and the most frequently used tests for SARS-CoV-2 both depend on the genomic and peptide sequences of the virus for their robustness. Therefore, understanding the mutation rates and content of the virus is critical. Two key proteins for SARS-CoV-2 infection and replication are the S protein, responsible for viral entry into the cells, and RdRp, the RNA polymerase responsible for replicating the viral genome. Due to their roles in the viral cycle, these proteins are crucial for the fitness and infectiousness of the virus. Our previous findings had shown that the two most frequently observed mutations in the SARS-CoV-2 genome, 14408C>T in the RdRp coding region, and 23403A>G in the S gene, are correlated with higher mutation density over time. In this study, we further detail the selection dynamics and the mutation rates of SARS-CoV-2 genes, comparing them between isolates carrying both mutations, and isolates carrying neither. We find that the S gene and the RdRp coding region show the highest variance between the genotypes, and their selection dynamics contrast each other over time. The S gene displays higher tolerance for positive selection in mutant isolates early during the appearance of the double mutant genotype, and undergoes increasing negative selection over time, whereas the RdRp region in the mutant isolates shows strong negative selection throughout the pandemic.

Indexed as

Genome, ViralPoint MutationCOVID-19Evolution, MolecularGene Expression Regulation, ViralGenotypeHumansMutation RateOpen Reading FramesRNA-Dependent RNA PolymeraseSARS-CoV-2Selection, GeneticSpike Glycoprotein, CoronavirusUnited KingdomUnited StatesRNA-Dependent RNA PolymeraseSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19Mutation ratesRdRpRNA-dependent RNA polymeraseSARS-CoV-2Surface glycoprotein

Identifiers

PMID33667722
PMCPMC7925239
OpenAlexW3133860031

What OpenQuestion holds

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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.