Evidence map›Paper›PMID 32886709›Full record

ArticlePLoS pathogens2020

Cross-utilisation of template RNAs by alphavirus replicases.

Laura Sandra Lello, Age Utt, Koen Bartholomeeusen, Sainan Wang, Kai Rausalu, Catherine Kendall, Sandra Coppens, Rennos Fragkoudis, Andrew Tuplin, Luke Alphey and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2020. 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
3.6field-weighted citation impact, top 6% 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, 31 citations in OpenAlex.

  1. Article
  2. Transgene sequence codon optimization and composition determines replication competence of self-amplifying RNA.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. The advent of clinical self-amplifying RNA vaccines.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Safety concern of recombination between self-amplifying mRNA vaccines and viruses is mitigated in vivo.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  12. Review
  13. Mimicking superinfection exclusion disrupts alphavirus infection and transmission in the yellow fever mosquitoProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  14. Article
  15. A trans-amplifying RNA simplified to essential elements is highly replicative and robustly immunogenic in mice.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  16. Trans-amplifying RNA: Translational application in gene therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  17. Article
  18. Review
  19. Article
  20. Article
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

12 authors at 6 institutions in 3 countries.

Laura Sandra LelloInstitute of Technology, University of Tartu, Tartu, Estonia.
Age UttInstitute of Technology, University of Tartu, Tartu, Estonia.ORCID 0000-0002-6709-2507
Koen BartholomeeusenDepartment of Biomedical Sciences, Institute of Tropical Medicine, Antwerpen, Belgium.
Sainan WangInstitute of Technology, University of Tartu, Tartu, Estonia.ORCID 0000-0002-7046-4965
Kai RausaluInstitute of Technology, University of Tartu, Tartu, Estonia.ORCID 0000-0002-8926-5907
Catherine KendallFaculty of Biological Sciences and Astbury Centre for Structural and Molecular Biology, University of Leeds, Leeds, United Kingdom.ORCID 0000-0002-1037-2436
Sandra CoppensDepartment of Biomedical Sciences, Institute of Tropical Medicine, Antwerpen, Belgium.
Rennos FragkoudisUniversity of Nottingham, School of Veterinary Medicine and Science, Loughborough, United Kingdom.
Andrew TuplinFaculty of Biological Sciences and Astbury Centre for Structural and Molecular Biology, University of Leeds, Leeds, United Kingdom.ORCID 0000-0003-2524-707X
Luke AlpheyThe Pirbright Institute, Woking, United Kingdom.ORCID 0000-0002-2916-3802
Kevin K AriënDepartment of Biomedical Sciences, Institute of Tropical Medicine, Antwerpen, Belgium.
Andres MeritsInstitute of Technology, University of Tartu, Tartu, Estonia.ORCID 0000-0001-8193-0071
University of Tartu · EEInstituut voor Tropische Geneeskunde · BEUniversity of Leeds · GBThe Pirbright Institute · GBUniversity of Antwerp · BEUniversity of Nottingham · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/E/I/00007033Biotechnology and Biological Sciences Research Council BBS/E/I/00007038Biotechnology and Biological Sciences Research Council BBS/E/I/00007039Medical Research Council MR/NO1054X/1Wellcome Trust 200171/Z/15/Z
6 · The paper itself

Abstract

Most alphaviruses (family Togaviridae) including Sindbis virus (SINV) and other human pathogens, are transmitted by arthropods. The first open reading frame in their positive strand RNA genome encodes for the non-structural polyprotein, a precursor to four separate subunits of the replicase. The replicase interacts with cis-acting elements located near the intergenic region and at the ends of the viral RNA genome. A trans-replication assay was developed and used to analyse the template requirements for nine alphavirus replicases. Replicases of alphaviruses of the Semliki Forest virus complex were able to cross-utilize each other's templates as well as those of outgroup alphaviruses. Templates of outgroup alphaviruses, including SINV and the mosquito-specific Eilat virus, were promiscuous; in contrast, their replicases displayed a limited capacity to use heterologous templates, especially in mosquito cells. The determinants important for efficient replication of template RNA were mapped to the 5' region of the genome. For SINV these include the extreme 5'- end of the genome and sequences corresponding to the first stem-loop structure in the 5' untranslated region. Mutations introduced in these elements drastically reduced infectivity of recombinant SINV genomes. The trans-replicase tools and approaches developed here can be instrumental in studying alphavirus recombination and evolution, but can also be applied to study other viruses such as picornaviruses, flaviviruses and coronaviruses.

Indexed as

AlphavirusGenome, ViralNucleic Acid ConformationRNA-Dependent RNA PolymeraseRNA, ViralViral ProteinsCell Line, TumorHEK293 CellsHumansRNA-Dependent RNA PolymeraseRNA, ViralViral Proteins

Identifiers

PMID32886709
PMCPMC7498090
OpenAlexW3083003653

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.