Evidence map›Paper›PMID 25385608›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

In vitro evolution of high-titer, virus-like vesicles containing a single structural protein.

Nina F Rose, Linda Buonocore, John B Schell, Anasuya Chattopadhyay, Kapil Bahl, Xinran Liu, John K Rose

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.4field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Rational design of self-amplifying virus-like vesicles with Ebola virus glycoprotein as vaccines.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  5. Article
  6. Article
  7. Viral Replicon Systems and Their Biosafety Aspects.Applied biosafety : journal of the American Biological Safety Association · 2023
    Review
  8. Article
  9. Article
  10. Advances in COVID-19 mRNA vaccine development.Signal transduction and targeted therapy · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Mechanisms of Innate Immune Activation by a Hybrid Alphavirus-Rhabdovirus Vaccine Platform.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2020
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Homologous recombination is an intrinsic defense against antiviral RNA interference.Proceedings of the National Academy of Sciences of the United States of America · 2018
    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 1 institution in 1 country.

Nina F RoseDepartment of Pathology, Yale University School of Medicine, New Haven, CT 06510; and.
Linda BuonocoreDepartment of Pathology, Yale University School of Medicine, New Haven, CT 06510; and.
John B SchellDepartment of Pathology, Yale University School of Medicine, New Haven, CT 06510; and.
Anasuya ChattopadhyayDepartment of Pathology, Yale University School of Medicine, New Haven, CT 06510; and.
Kapil BahlDepartment of Pathology, Yale University School of Medicine, New Haven, CT 06510; and.
Xinran LiuCenter for Cellular and Molecular Imaging, Yale University School of Medicine, New Haven, CT 06510.
John K RoseDepartment of Pathology, Yale University School of Medicine, New Haven, CT 06510; and john.rose@yale.edu.
Yale University · US

Funding

Yale University Clinical and Translational Science Award ProgramUL1TR000142 · NCATS · YALE UNIVERSITY · PI SHERWIN, ROBERT S · 2012 to 2015
$31.8M
IMMUNE RESPONSES TO VSV/HIV/SIV HYBRIDS IN MACAQUESR01AI045510 · NIAID · YALE UNIVERSITY · PI ROSE, JOHN K. · 1999 to 2010
$6.4M
Development of VSV/HIV Recombinants as HIV VaccinesR37AI040357 · NIAID · YALE UNIVERSITY · PI ROSE, JOHN K. · 2003 to 2012
$3.1M
NCATS NIH HHS UL1 TR000142NIAID NIH HHS R01 AI045510NIAID NIH HHS R01AI-045510NIAID NIH HHS R37 AI040357NIAID NIH HHS R37AI-040357
6 · The paper itself

Abstract

Self-propagating, infectious, virus-like vesicles (VLVs) are generated when an alphavirus RNA replicon expresses the vesicular stomatitis virus glycoprotein (VSV G) as the only structural protein. The mechanism that generates these VLVs lacking a capsid protein has remained a mystery for over 20 years. We present evidence that VLVs arise from membrane-enveloped RNA replication factories (spherules) containing VSV G protein that are largely trapped on the cell surface. After extensive passaging, VLVs evolve to grow to high titers through acquisition of multiple point mutations in their nonstructural replicase proteins. We reconstituted these mutations into a plasmid-based system from which high-titer VLVs can be recovered. One of these mutations generates a late domain motif (PTAP) that is critical for high-titer VLV production. We propose a model in which the VLVs have evolved in vitro to exploit a cellular budding pathway that is hijacked by many enveloped viruses, allowing them to bud efficiently from the cell surface. Our results suggest a basic mechanism of propagation that may have been used by primitive RNA viruses lacking capsid proteins. Capsids may have evolved later to allow more efficient packaging of RNA, greater virus stability, and evasion of innate immunity.

Indexed as

Biological EvolutionAlphavirusAmino Acid MotifsIn Vitro TechniquesMicroscopy, Electron, TransmissionViral Structural ProteinsViral Structural Proteinsevolutionlate domainSFV repliconVSV glycoprotein

Identifiers

PMID25385608
PMCPMC4250146
OpenAlexW2050133902

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.