Evidence map›Paper›PMID 22837419›Full record

ArticleThe Journal of general virology2012

Genomic analysis of 16 Colorado human NL63 coronaviruses identifies a new genotype, high sequence diversity in the N-terminal domain of the spike gene and evidence of recombination.

Samuel R Dominguez, Gregory E Sims, David E Wentworth, Rebecca A Halpin, Christine C Robinson, Christopher D Town, Kathryn V Holmes

Abstract read
In one paragraph

Article in The Journal of general virology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
5.1field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 33 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

7 authors at 3 institutions in 1 country.

Samuel R DominguezDepartment of Microbiology, University of Colorado School of Medicine, Anschutz Medical Campus, 12800 E 19th Ave, Room P18-9403B, Aurora, CO 80045, USA.
Gregory E SimsJ. Craig Venter Institute, 9704 Medical Center Drive, Rockville, MD 20850, USA.
David E WentworthJ. Craig Venter Institute, 9704 Medical Center Drive, Rockville, MD 20850, USA.
Rebecca A HalpinJ. Craig Venter Institute, 9704 Medical Center Drive, Rockville, MD 20850, USA.
Christine C RobinsonDepartment of Pathology and Clinical Medicine, Children's Hospital Colorado, 13123 E 16th Ave, Aurora, CO 80045, USA.
Christopher D TownJ. Craig Venter Institute, 9704 Medical Center Drive, Rockville, MD 20850, USA.
Kathryn V HolmesDepartment of Microbiology, University of Colorado School of Medicine, Anschutz Medical Campus, 12800 E 19th Ave, Room P18-9403B, Aurora, CO 80045, USA.
J. Craig Venter Institute · USUniversity of Colorado Anschutz Medical Campus · USChildren's Hospital Colorado · US

Funding

Epidemiology and Pathogenesis of Novel CoronavirusesK08AI073525 · NIAID · UNIVERSITY OF COLORADO DENVER · PI DOMINGUEZ, SAMUEL RICHARD · 2008 to 2012
$761k
Intramural NIH HHSNIAID NIH HHS 1-K08AI073525NIAID NIH HHS HHSN272200900007CNIAID NIH HHS K08 AI073525
6 · The paper itself

Abstract

This study compared the complete genome sequences of 16 NL63 strain human coronaviruses (hCoVs) from respiratory specimens of paediatric patients with respiratory disease in Colorado, USA, and characterized the epidemiology and clinical characteristics associated with circulating NL63 viruses over a 3-year period. From 1 January 2009 to 31 December 2011, 92 of 9380 respiratory specimens were found to be positive for NL63 RNA by PCR, an overall prevalence of 1 %. NL63 viruses were circulating during all 3 years, but there was considerable yearly variation in prevalence and the month of peak incidence. Phylogenetic analysis comparing the genome sequences of the 16 Colorado NL63 viruses with those of the prototypical hCoV-NL63 and three other NL63 viruses from the Netherlands demonstrated that there were three genotypes (A, B and C) circulating in Colorado from 2005 to 2010, and evidence of recombination between virus strains was found. Genotypes B and C co-circulated in Colorado in 2005, 2009 and 2010, but genotype A circulated only in 2005 when it was the predominant NL63 strain. Genotype C represents a new lineage that has not been described previously. The greatest variability in the NL63 virus genomes was found in the N-terminal domain (NTD) of the spike gene (nt 1-600, aa 1-200). Ten different amino acid sequences were found in the NTD of the spike protein among these NL63 strains and the 75 partial published sequences of NTDs from strains found at different times throughout the world.

Indexed as

Genetic VariationGenotypeRecombination, GeneticAdolescentChildChild, PreschoolColoradoCoronavirus InfectionsCoronavirus NL63, HumanFemaleGenome, ViralHumansInfantInfant, NewbornMaleMembrane GlycoproteinsMembrane GlycoproteinsSpike Glycoprotein, CoronavirusViral Envelope Proteins

Identifiers

PMID22837419
PMCPMC4091283
OpenAlexW2138280137

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.