Evidence map›Paper›PMID 18474558›Full record

ArticleThe Journal of general virology2008

Genomic and biological characterization of aggressive and docile strains of lymphocytic choriomeningitis virus rescued from a plasmid-based reverse-genetics system.

Minjie Chen, Shuiyun Lan, Rong Ou, Graeme E Price, Hong Jiang, Juan Carlos de la Torre, Demetrius Moskophidis

Open access · greenAbstract readComparative Study
In one paragraph

Article in The Journal of general virology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Chronic infection perturbs the affinity hierarchy of antiviral B cells.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. A unique variant of lymphocytic choriomeningitis virus that induces pheromone binding protein MUP: Critical role for CTL.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  7. Arenavirus Quasispecies and Their Biological Implications.Current topics in microbiology and immunology · 2016
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. 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 at 2 institutions in 1 country.

Minjie ChenCenter for Molecular Chaperones/Radiobiology and Cancer Virology, Medical College of Georgia, Augusta, GA 30912, USA.
Shuiyun LanCenter for Molecular Chaperones/Radiobiology and Cancer Virology, Medical College of Georgia, Augusta, GA 30912, USA.
Rong OuCenter for Molecular Chaperones/Radiobiology and Cancer Virology, Medical College of Georgia, Augusta, GA 30912, USA.
Graeme E PriceCenter for Molecular Chaperones/Radiobiology and Cancer Virology, Medical College of Georgia, Augusta, GA 30912, USA.
Hong JiangCenter for Molecular Chaperones/Radiobiology and Cancer Virology, Medical College of Georgia, Augusta, GA 30912, USA.
Juan Carlos de la TorreMolecular Integrative Neuroscience Department (MIND), The Scripps Research Institute, La Jolla, CA 92037, USA.
Demetrius MoskophidisCenter for Molecular Chaperones/Radiobiology and Cancer Virology, Medical College of Georgia, Augusta, GA 30912, USA.
Augusta University · USScripps Research Institute · US

Funding

REVERSE GENETICS OF ARENAVIRUSESR01AI047140 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI DE LA TORRE, JUAN C. · 2001 to 2011
$3.0M
PERSISTENCE OF LCMV BY EXHAUSTION OF CYTOTOXIC T CELLSR01AI042114 · NIAID · MEDICAL COLLEGE OF GEORGIA (MCG) · PI MOSKOFIDIS, DIMITRIOS · 1998 to 2006
$1.9M
NIAID NIH HHS AI42114NIAID NIH HHS R01 AI042114NIAID NIH HHS R01 AI047140
6 · The paper itself

Abstract

Arenaviruses include several causative agents of haemorrhagic fever disease in humans. In addition, the prototypic arenavirus lymphocytic choriomeningitis virus (LCMV) is a superb model for the study of virus-host interactions, including the basis of viral persistence and associated diseases. There is little understanding about the molecular mechanisms concerning the regulation and specific role of viral proteins in modulating arenavirus-host cell interactions either associated with an acute or persistent infection, and associated disease. Here, we report the genomic and biological characterization of LCMV strains 'Docile' (persistent) and 'Aggressive' (not persistent) recovered from cloned cDNA via reverse genetics. Our results confirmed that the cloned viruses accurately recreated the in vivo phenotypes associated with the corresponding natural Docile and Aggressive viral isolates. In addition, we provide evidence that the ability of the Docile strain to persist is determined by the nature of both S and L RNA segments. Thus, our findings provide the foundation for studies aimed at gaining a detailed understanding of viral determinants of LCMV persistence in its natural host, which may aid in the development of vaccines to prevent or treat the diseases caused by arenaviruses in humans.

Indexed as

PlasmidsAnimalsCell LineCricetinaeHost-Pathogen InteractionsLymphocytic ChoriomeningitisLymphocytic choriomeningitis virusMiceMice, Inbred C57BLReassortant VirusesRNA, ViralRodent DiseasesSequence Analysis, RNAVirulenceRNA, Viral

Identifiers

PMID18474558
PMCPMC2652504
OpenAlexW70708574

What OpenQuestion holds

Textmetadata
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.