Evidence map›Paper›PMID 31548390›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Structural and functional analyses reveal promiscuous and species specific use of ephrin receptors by Cedar virus.

Eric D Laing, Chanakha K Navaratnarajah, Sofia Cheliout Da Silva, Stephanie R Petzing, Yan Xu, Spencer L Sterling, Glenn A Marsh, Lin-Fa Wang, Moushimi Amaya, Dimitar B Nikolov and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

53 citing papers in PubMed, 67 citations in OpenAlex.

  1. One health (Amsterdam, Netherlands) · 2026
    Review
  2. Article
  3. Article
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  7. Article
  8. Review
  9. Dengue Virus NS1 Binds Ephrin B1 to Trigger Endothelial Dysfunction.bioRxiv : the preprint server for biology · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Review
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  15. Article
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  18. Article
  19. Review
  20. Molecular determinants of cross-species transmission in emerging viral infections.Microbiology and molecular biology reviews : MMBR · 2024
    Review
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

13 authors at 5 institutions in 3 countries.

Eric D LaingDepartment of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814.
Chanakha K NavaratnarajahDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN 55905.
Sofia Cheliout Da SilvaDepartment of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814.
Stephanie R PetzingDepartment of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814.
Yan XuStructural Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065.
Spencer L SterlingDepartment of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814.
Glenn A MarshCommonwealth Scientific and Industrial Research Organization Australian Animal Health Laboratory, Geelong, VIC 3219, Australia.
Lin-Fa WangProgramme in Emerging Infectious Diseases, Duke-National University of Singapore Medical School, Singapore 169857.ORCID 0000-0003-2752-0535
Moushimi AmayaDepartment of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814.
Dimitar B NikolovStructural Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065.
Roberto CattaneoDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN 55905.ORCID 0000-0001-6881-2548
Christopher C BroderDepartment of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814; christopher.broder@usuhs.edu xukai99@gmail.com.ORCID 0000-0001-5382-0510
Kai XuStructural Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065; christopher.broder@usuhs.edu xukai99@gmail.com.ORCID 0000-0001-5412-6942
Uniformed Services University of the Health Sciences · USMemorial Sloan Kettering Cancer Center · USMayo Clinic in Arizona · USAustralian Centre for Disease Preparedness · AUNational University of Singapore · SG

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
STRUCTURAL STUDY OF EPH RECEPTORS AND EPHRINSR01NS038486 · NINDS · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI NIKOLOV, DIMITAR B · 1999 to 2018
$5.9M
Vaccines and Therapeutics for Nipah and Hendra virusU01AI077995 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI BRODER, CHRISTOPHER C · 2008 to 2012
$5.5M
Nipah Virus and Hendra Virus Entry and Virion AssemblyR01AI054715 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI BRODER, CHRISTOPHER C · 2006 to 2016
$3.1M
A Recombinant Cedar Virus-based Henipavirus Replication Platform for High-throughput Inhibitor ScreeningR21AI137813 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI BRODER, CHRISTOPHER C, RONG, LIJUN · 2018 to 2019
$425k
NCI NIH HHS P30 CA008748NIAID NIH HHS R01 AI054715NIAID NIH HHS R21 AI137813NIAID NIH HHS U01 AI077995NINDS NIH HHS R01 NS038486
6 · The paper itself

Abstract

Cedar virus (CedV) is a bat-borne henipavirus related to Nipah virus (NiV) and Hendra virus (HeV), zoonotic agents of fatal human disease. CedV receptor-binding protein (G) shares only ∼30% sequence identity with those of NiV and HeV, although they can all use ephrin-B2 as an entry receptor. We demonstrate that CedV also enters cells through additional B- and A-class ephrins (ephrin-B1, ephrin-A2, and ephrin-A5) and report the crystal structure of the CedV G ectodomain alone and in complex with ephrin-B1 or ephrin-B2. The CedV G receptor-binding site is structurally distinct from other henipaviruses, underlying its capability to accommodate additional ephrin receptors. We also show that CedV can enter cells through mouse ephrin-A1 but not human ephrin-A1, which differ by 1 residue in the key contact region. This is evidence of species specific ephrin receptor usage by a henipavirus, and implicates additional ephrin receptors in potential zoonotic transmission.

Indexed as

AnimalsCell FusionEphrin-B1Ephrin-B2Ephrin-B3HenipavirusHenipavirus InfectionsHumansMiceMutationProtein BindingProtein ConformationReceptors, VirusSpecies SpecificityViral Envelope ProteinsVirus Internalizationattachment protein GEphrin-B1Ephrin-B2Ephrin-B3Receptors, VirusViral Envelope ProteinsCedar virusentryephrinshenipavirusesvirus receptors

Identifiers

PMID31548390
PMCPMC6789926
OpenAlexW2975394596

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.