Evidence map›Paper›PMID 23559477›Full record

ArticleThe Journal of general virology2013

An infectious recombinant foot-and-mouth disease virus expressing a fluorescent marker protein.

Julian Seago, Nicholas Juleff, Katy Moffat, Stephen Berryman, John M Christie, Bryan Charleston, Terry Jackson

Abstract read
In one paragraph

Article in The Journal of general virology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Infectious Recombinant Senecavirus A Expressing p16International journal of molecular sciences · 2023
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Emergency Services of Viral RNAs: Repair and Remodeling.Microbiology and molecular biology reviews : MMBR · 2018
    Review
  16. Article
  17. Article
  18. 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

7 authors.

Julian SeagoThe Pirbright Institute, Woking, Surrey GU24 0NF, UK.
Nicholas JuleffThe Pirbright Institute, Woking, Surrey GU24 0NF, UK.
Katy MoffatThe Pirbright Institute, Woking, Surrey GU24 0NF, UK.
Stephen BerrymanThe Pirbright Institute, Woking, Surrey GU24 0NF, UK.
John M ChristieInstitute of Molecular Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow G12 8QQ, UK.
Bryan CharlestonThe Pirbright Institute, Woking, Surrey GU24 0NF, UK.
Terry JacksonThe Pirbright Institute, Woking, Surrey GU24 0NF, UK.

Funding

Biotechnology and Biological Sciences Research Council BBS/E/I/00001709Biotechnology and Biological Sciences Research Council BBS/E/I/00001715Wellcome Trust 089755
6 · The paper itself

Abstract

Foot-and-mouth disease virus (FMDV) is one of the most extensively studied animal pathogens because it remains a major threat to livestock economies worldwide. However, the dynamics of FMDV infection are still poorly understood. The application of reverse genetics provides the opportunity to generate molecular tools to further dissect the FMDV life cycle. Here, we have used reverse genetics to determine the capsid packaging limitations for a selected insertion site in the FMDV genome. We show that exogenous RNA up to a defined length can be stably introduced into the FMDV genome, whereas larger insertions are excised by recombination events. This led us to construct a recombinant FMDV expressing the fluorescent marker protein, termed iLOV. Characterization of infectious iLOV-FMDV showed the virus has a plaque morphology and rate of growth similar to the parental virus. In addition, we show that cells infected with iLOV-FMDV are easily differentiated by flow cytometry using the inherent fluorescence of iLOV and that cells infected with iLOV-FMDV can be monitored in real-time with fluorescence microscopy. iLOV-FMDV therefore offers a unique tool to characterize FMDV infection in vitro, and its applications for in vivo studies are discussed.

Indexed as

Recombination, GeneticAnimalsCells, CulturedCytopathogenic Effect, ViralEpitheliumFlow CytometryFoot-and-Mouth DiseaseFoot-and-Mouth Disease VirusGoatsGreen Fluorescent ProteinsGreen Fluorescent Proteins

Identifiers

PMID23559477
PMCPMC3709630

What OpenQuestion holds

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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.