Evidence map›Paper›PMID 15939791›Full record

ArticleThe Journal of experimental medicine2005

Divergent and convergent evolution after a common-source outbreak of hepatitis C virus.

Stuart C Ray, Liam Fanning, Xiao-Hong Wang, Dale M Netski, Elizabeth Kenny-Walsh, David L Thomas

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed
10.4field-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

94 citing papers in PubMed, 187 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. CD8Frontiers in immunology · 2022
    Article
  7. Article
  8. Review
  9. Adaptive Immune Response against Hepatitis C Virus.International journal of molecular sciences · 2020
    Review
  10. Inconsistent temporal patterns of genetic variation of HCV among high-risk subjects may impact inference of transmission networks.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2019
    Article
  11. Review
  12. Differential escape of HCV from CD8Journal of viral hepatitis · 2019
    Article
  13. Neutral Theory and Rapidly Evolving Viral Pathogens.Molecular biology and evolution · 2018
    Article
  14. Evidence of CD4Scientific reports · 2018
    Article
  15. Complex patterns of Hepatitis-C virus longitudinal clustering in a high-risk population.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2018
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

34 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

6 authors at 4 institutions in 3 countries.

Stuart C RayDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA. sray@jhmi.edu
Liam Fanning
Xiao-Hong Wang
Dale M Netski
Elizabeth Kenny-Walsh
David L Thomas
Johns Hopkins Medicine · USNational University of Ireland · IEArmy Medical University · CNJohns Hopkins University · US

Funding

Virus-Host Interactions in Hepatitis C Virus (HCV) InfectionsU19AI040035 · NIAID · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI THOMAS, DAVID L · 1996 to 2009
$12.0M
The Progression of Hepatitis C Among IDUs with HIVR01DA016078 · NIDA · JOHNS HOPKINS UNIVERSITY · PI BALAGOPAL, ASHWIN, THOMAS, DAVID L · 2002 to 2016
$10.9M
NIAID NIH HHS U19 AI040035NIAID NIH HHS U19 AI40035NIDA NIH HHS R01 DA016078
6 · The paper itself

Abstract

The genomic sequences of viruses that are highly mutable and cause chronic infection tend to diverge over time. We report that these changes represent both immune-driven selection and, in the absence of immune pressure, reversion toward an ancestral consensus. Sequence changes in hepatitis C virus (HCV) structural and nonstructural genes were studied in a cohort of women accidentally infected with HCV in a rare common-source outbreak. We compared sequences present in serum obtained 18-22 yr after infection to sequences present in the shared inoculum and found that HCV evolved along a distinct path in each woman. Amino acid substitutions in known epitopes were directed away from consensus in persons having the HLA allele associated with that epitope (immune selection), and toward consensus in those lacking the allele (reversion). These data suggest that vaccines for genetically diverse viruses may be more effective if they represent consensus sequence, rather than a human isolate.

Indexed as

Evolution, MolecularAllelesAmino Acid SubstitutionAnimalsConsensus SequenceEpitopes, T-LymphocyteHepacivirusHepatitis CHepatitis C AntigensHLA AntigensMiceSelection, GeneticViral Hepatitis VaccinesViral Structural ProteinsEpitopes, T-LymphocyteHepatitis C AntigensHLA AntigensViral Hepatitis VaccinesViral Structural Proteins

Identifiers

PMID15939791
PMCPMC2213258
OpenAlexW2098062401

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.