Evidence map›Paper›PMID 31641088›Full record

ArticlemBio2019

Attenuation of Live-Attenuated Yellow Fever 17D Vaccine Virus Is Localized to a High-Fidelity Replication Complex.

Emily H Davis, Andrew S Beck, Ashley E Strother, Jill K Thompson, Steven G Widen, Stephen Higgs, Thomas G Wood, Alan D T Barrett

Open access · goldAbstract read
In one paragraph

Article in mBio, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  3. Review
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  5. West Nile virus unmasked: from gene variability to future challenges.Frontiers in cellular and infection microbiology · 2025
    Review
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  7. Article
  8. Replication Kinetics of a Candidate Live-Attenuated Vaccine for Cache Valley Virus inVector borne and zoonotic diseases (Larchmont, N.Y.) · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Intra-Host Diversity of Dengue Virus in Mosquito Vectors.Frontiers in cellular and infection microbiology · 2022
    Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  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

8 authors at 2 institutions in 1 country.

Emily H Davis *Department of Pathology, The University of Texas Medical Branch, Galveston, Texas, USA.
Andrew S Beck *Department of Pathology, The University of Texas Medical Branch, Galveston, Texas, USA.
Ashley E StrotherDepartment of Pathology, The University of Texas Medical Branch, Galveston, Texas, USA.
Jill K ThompsonDepartment of Biochemistry and Molecular Biology, The University of Texas Medical Branch, Galveston, Texas, USA.
Steven G WidenDepartment of Biochemistry and Molecular Biology, The University of Texas Medical Branch, Galveston, Texas, USA.
Stephen HiggsBiosecurity Research Institute, Kansas State University, Manhattan, Kansas, USA.
Thomas G WoodDepartment of Biochemistry and Molecular Biology, The University of Texas Medical Branch, Galveston, Texas, USA.
Alan D T BarrettDepartment of Pathology, The University of Texas Medical Branch, Galveston, Texas, USA abarrett@utmb.edu.
The University of Texas Medical Branch at Galveston · USKansas State University · US

Funding

Biodefense Training ProgramT32AI060549 · NIAID · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI ASHOK K CHOPRA, Janice J Endsley · 2004 to 2026
$3.0M
Next Generation sequencing of yellow fever 17D vaccine virusR21AI113407 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI BARRETT, ALAN D.T. · 2015 to 2016
$426k
NIAID NIH HHS R21 AI113407NIAID NIH HHS T32 AI060549
6 · The paper itself

Abstract

The molecular basis of attenuation for live-attenuated vaccines is poorly understood. The yellow fever (YF) 17D vaccine virus was derived from the wild-type, parental strain Asibi virus by serial passage in chicken tissue and has proven to be a very safe and efficacious vaccine. We have previously shown that wild-type Asibi is a typical RNA virus with high genetic diversity, while the 17D vaccine virus has very little genetic diversity. To investigate this further, we treated Asibi and 17D viruses with ribavirin, a GTP analog with strong antiviral activity that increases levels of mutations in the viral genome. As expected, ribavirin treatment introduced mutations into the Asibi virus genome at a very high frequency and decreased viral infectivity while, in contrast, the 17D vaccine virus was resistant to ribavirin, as treatment with the antiviral introduced very few mutations into the genome, and viral infectivity was not lost. The results were confirmed for another YF wild-type parental and vaccine pair, a wild-type French viscerotropic virus and French neurotropic vaccine. Using recombinant Asibi and 17D viruses, ribavirin sensitivity was located to viral nonstructural genes. Thus, two live-attenuated YF vaccine viruses are genetically stable even under intense mutagenic pressure, suggesting that attenuation of live-attenuated YF vaccines is due, at least in part, to fidelity of the replication complex resulting in high genetic stability.

Indexed as

AnimalsAntiviral AgentsGenetic VariationHumansPolymorphism, Single NucleotideRibavirinVaccines, AttenuatedYellow FeverYellow Fever VaccineYellow fever virusAntiviral AgentsRibavirinVaccines, AttenuatedYellow Fever Vaccineattenuationlive virus vaccinequasispeciesribavirinvaccineyellow fever

Identifiers

PMID31641088
PMCPMC6805994
OpenAlexW2982164257

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.