Evidence map›Paper›PMID 26457367›Full record

ArticleVirology2015

Replacement of the hepatitis E virus ORF3 protein PxxP motif with heterologous late domain motifs affects virus release via interaction with TSG101.

Scott P Kenney, Jacquelyn L Wentworth, Connie L Heffron, Xiang-Jin Meng

Open access · greenAbstract read
In one paragraph

Article in Virology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Morphogenesis of Hepatitis E Virus.Advances in experimental medicine and biology · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Structural and molecular biology of hepatitis E virus.Computational and structural biotechnology journal · 2021
    Review
  11. Article
  12. Stem Cell-Derived Culture Models of Hepatitis E Virus Infection.Cold Spring Harbor perspectives in medicine · 2019
    Review
  13. Evolutionary Origins of Enteric Hepatitis Viruses.Cold Spring Harbor perspectives in medicine · 2018
    Review
  14. Article
  15. Article
  16. Hepatitis E virus: advances and challenges.Nature reviews. Gastroenterology & hepatology · 2018
    Review
  17. Article
  18. Hepatitis E virus ORF3 is a functional ion channel required for release of infectious particles.Proceedings of the National Academy of Sciences of the United States of America · 2017
    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

4 authors at 3 institutions in 1 country.

Scott P KenneyDepartment of Biomedical Sciences and Pathobiology, College of Veterinary Medicine, Virginia Polytechnic Institute and State University (Virginia Tech), Blacksburg, VA, USA.
Jacquelyn L WentworthVirginia Tech Carilion School of Medicine, Roanoke, VA, USA.
Connie L HeffronDepartment of Biomedical Sciences and Pathobiology, College of Veterinary Medicine, Virginia Polytechnic Institute and State University (Virginia Tech), Blacksburg, VA, USA.
Xiang-Jin MengDepartment of Biomedical Sciences and Pathobiology, College of Veterinary Medicine, Virginia Polytechnic Institute and State University (Virginia Tech), Blacksburg, VA, USA. Electronic address: xjmeng@vt.edu.
Virginia Tech · USCarilion Clinic · USVirginia–Maryland College of Veterinary Medicine · US

Funding

A Chicken Model to Study Hepatitis E Virus PathogenesisR01AI050611 · NIAID · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI MENG, XIANG-JIN · 2002 to 2023
$6.1M
Mechanism of Hepatitis E Virus Replication and PathogenesisR01AI074667 · NIAID · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI MENG, XIANG-JIN · 2008 to 2016
$3.1M
NIAID NIH HHS R01 AI050611NIAID NIH HHS R01 AI074667
6 · The paper itself

Abstract

The ORF3 protein of hepatitis E virus (HEV) contains a "PSAP" amino acid late domain motif, which allows for interaction with the endosomal sorting complexes required for transport (ESCRT) pathway aiding virion release. Late domain motifs are interchangeable with other viral late domain motifs in several enveloped viruses, however, it remains unknown whether HEV shares this functional interchangeability and what implications this might have on viral replication. In this study, by substituting heterologous late domain motifs (PPPY, YPDL, and PSAA) for the HEV ORF3 late domain (PSAP), we demonstrated that deviation from the PSAP motif reduces virus release as measured by viral RNA in culture media. Virus release could not be restored by insertion of a heterologous late domain motif or by supplying wild-type ORF3 in trans, suggesting that the HEV PSAP motif is required for viral exit which cannot be bypassed by the use of alternative heterologous late domains.

Indexed as

Virus ReleaseAmino Acid MotifsDNA-Binding ProteinsEndosomal Sorting Complexes Required for TransportHepatitis EHepatitis E virusHost-Pathogen InteractionsHumansProtein BindingProtein Structure, TertiaryTranscription FactorsTsg101 ProteinViral ProteinsVirus ReplicationDNA-Binding ProteinsEndosomal Sorting Complexes Required for TransportORF3 protein, Hepatitis E virusTranscription FactorsTsg101 ProteinViral ProteinsHepatitis E virus (HEV)Late domainOpen reading frame 3 (ORF3)PxxP motifVirus release

Identifiers

PMID26457367
PMCPMC4679584
OpenAlexW1913238803

What OpenQuestion holds

Textmetadata
LicenceTDM
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.