Evidence map›Paper›PMID 21307223›Full record

ArticleThe Journal of general virology2011

Discovery of a small arterivirus gene that overlaps the GP5 coding sequence and is important for virus production.

Andrew E Firth, Jessika C Zevenhoven-Dobbe, Norma M Wills, Yun Young Go, Udeni B R Balasuriya, John F Atkins, Eric J Snijder, Clara C Posthuma

Open access · greenAbstract read
In one paragraph

Article in The Journal of general virology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 146 papers.

0numbers the graph read from it
0cells of the map it votes in
146citing papers in PubMed
46.6field-weighted citation impact, top 1% 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

146 citing papers in PubMed, 298 citations in OpenAlex.

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  13. Genetic variation and recombination analysis of theFrontiers in veterinary science · 2024
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  16. Review
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  20. Frontiers in microbiology · 2023
    Article

86 more citing papers are in PubMed but not listed here.

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

8 authors at 4 institutions in 4 countries.

Andrew E FirthDepartment of Pathology, University of Cambridge, Cambridge, UK.
Jessika C Zevenhoven-DobbeMolecular Virology Laboratory, Department of Medical Microbiology, Center of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Norma M WillsDepartment of Human Genetics, University of Utah, Salt Lake City, UT 84112-5330, USA.
Yun Young GoDepartment of Veterinary Science, Maxwell H. Gluck Equine Research Center, University of Kentucky, Lexington, KY 40546-0099, USA.
Udeni B R BalasuriyaDepartment of Veterinary Science, Maxwell H. Gluck Equine Research Center, University of Kentucky, Lexington, KY 40546-0099, USA.
John F AtkinsBioSciences Institute, University College Cork, Cork, Ireland.
Eric J SnijderMolecular Virology Laboratory, Department of Medical Microbiology, Center of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Clara C PosthumaMolecular Virology Laboratory, Department of Medical Microbiology, Center of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Leiden University Medical Center · NLUniversity of Kentucky · USUniversity of Utah · USUniversity of Cambridge · GB

Funding

The range of recoding and analysis of a 50 nt bypass to probe ribosomal functionR01GM079523 · NIGMS · UNIVERSITY OF UTAH · PI ATKINS, JOHN F. · 2007 to 2010
$1.3M
NIGMS NIH HHS R01 GM079523Wellcome Trust 088789
6 · The paper itself

Abstract

The arterivirus family (order Nidovirales) of single-stranded, positive-sense RNA viruses includes porcine respiratory and reproductive syndrome virus and equine arteritis virus (EAV). Their replicative enzymes are translated from their genomic RNA, while their seven structural proteins are encoded by a set of small, partially overlapping genes in the genomic 3'-proximal region. The latter are expressed via synthesis of a set of subgenomic mRNAs that, in general, are functionally monocistronic (except for a bicistronic mRNA encoding the E and GP2 proteins). ORF5, which encodes the major glycoprotein GP5, has been used extensively for phylogenetic analyses. However, an in-depth computational analysis now reveals the arterivirus-wide conservation of an additional AUG-initiated ORF, here termed ORF5a, that overlaps the 5' end of ORF5. The pattern of substitutions across sequence alignments indicated that ORF5a is subject to functional constraints at the amino acid level, while an analysis of substitutions at synonymous sites in ORF5 revealed a greatly reduced frequency of substitution in the portion of ORF5 that is overlapped by ORF5a. The 43-64 aa ORF5a protein and GP5 are probably expressed from the same subgenomic mRNA, via a translation initiation mechanism involving leaky ribosomal scanning. Inactivation of ORF5a expression by reverse genetics yielded a severely crippled EAV mutant, which displayed lower titres and a tiny plaque phenotype. These defects, which could be partially complemented in ORF5a-expressing cells, indicate that the novel protein, which may be the eighth structural protein of arteriviruses, is expressed and important for arterivirus infection.

Indexed as

Amino Acid SequenceAmino Acid SubstitutionAntigens, ViralBase SequenceConserved SequenceEquartevirusGene SilencingMolecular Sequence DataPorcine respiratory and reproductive syndrome virusSequence Homology, Amino AcidViral Envelope ProteinsViral Plaque AssayViral Structural ProteinsVirus ReplicationAntigens, Viralglycoprotein 5, PRRSVGP5 protein, equine arteritis virusViral Envelope ProteinsViral Structural Proteins

Identifiers

PMID21307223
PMCPMC3139419
OpenAlexW2100618023

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.