Evidence map›Paper›PMID 28196955›Full record

ArticlemBio2017

Identification of Human Junctional Adhesion Molecule 1 as a Functional Receptor for the Hom-1 Calicivirus on Human Cells.

Stanislav V Sosnovtsev, Carlos Sandoval-Jaime, Gabriel I Parra, Christine M Tin, Ronald W Jones, Jo Soden, Donna Barnes, Jim Freeth, Alvin W Smith, Kim Y Green

Open access · goldAbstract read
In one paragraph

Article in mBio, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.4field-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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Bile acids and ceramide overcome the entry restriction for GII.3 human norovirus replication in human intestinal enteroids.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  8. Review
  9. Article
  10. Review
  11. Viruses · 2019
    Review
  12. Article
  13. Virus recognition of glycan receptors.Current opinion in virology · 2019
    Review
  14. Immune Response Modulation by Caliciviruses.Frontiers in immunology · 2019
    Review
  15. Article
  16. Structural basis for murine norovirus engagement of bile acids and the CD300lf receptor.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  17. Review
  18. Article
  19. 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

10 authors at 2 institutions in 1 country.

Stanislav V SosnovtsevCaliciviruses Section, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, Maryland, USA ss216m@nih.gov.
Carlos Sandoval-JaimeCaliciviruses Section, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, Maryland, USA.
Gabriel I ParraCaliciviruses Section, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, Maryland, USA.
Christine M TinCaliciviruses Section, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, Maryland, USA.
Ronald W JonesCaliciviruses Section, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, Maryland, USA.
Jo SodenRetrogenix Ltd., Whaley Bridge, High Peak, United Kingdom.
Donna BarnesRetrogenix Ltd., Whaley Bridge, High Peak, United Kingdom.
Jim FreethRetrogenix Ltd., Whaley Bridge, High Peak, United Kingdom.
Alvin W SmithLaboratory for Calicivirus Studies, Oregon State University, Corvallis, Oregon, USA.
Kim Y GreenCaliciviruses Section, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, Maryland, USA.
National Institute of Allergy and Infectious Diseases · USOregon State University · US

Funding

Noroviruses and Epidemic GastroenteritisZIAAI000897 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI GREEN, KIM Y. · 2009 to 2025
$29.6M
6 · The paper itself

Abstract

The Hom-1 vesivirus was reported in 1998 following the inadvertent transmission of the animal calicivirus San Miguel sea lion virus to a human host in a laboratory. We characterized the Hom-1 strain and investigated the mechanism by which human cells could be infected. An expression library of 3,559 human plasma membrane proteins was screened for reactivity with Hom-1 virus-like particles, and a single interacting protein, human junctional adhesion molecule 1 (hJAM1), was identified. Transient expression of hJAM1 conferred susceptibility to Hom-1 infection on nonpermissive Chinese hamster ovary (CHO) cells. Virus infection was markedly inhibited when CHO cells stably expressing hJAM were pretreated with anti-hJAM1 monoclonal antibodies. Cell lines of human origin were tested for growth of Hom-1, and efficient replication was observed in HepG2, HuH7, and SK-CO15 cells. The three cell lines (of hepatic or intestinal origin) were confirmed to express hJAM1 on their surface, and clustered regularly interspaced short palindromic repeats/Cas9-mediated knockout of the hJAM1 gene in each line abolished Hom-1 propagation. Taken together, our data indicate that entry of the Hom-1 vesivirus into these permissive human cell lines is mediated by the plasma membrane protein hJAM1 as a functional receptor.

Indexed as

Virus ReplicationAnimalsCatsCell Adhesion MoleculesCell MembraneCHO CellsCricetinaeCricetulusHumansReceptors, Cell SurfaceReceptors, VirusVesivirusCell Adhesion MoleculesF11R protein, humanReceptors, Cell SurfaceReceptors, Virus

Identifiers

PMID28196955
PMCPMC5312078
OpenAlexW2588214353

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.