Evidence map›Paper›PMID 30111564›Full record

ArticleJournal of virology2018

The Human Cytomegalovirus Trimer and Pentamer Promote Sequential Steps in Entry into Epithelial and Endothelial Cells at Cell Surfaces and Endosomes.

Jing Liu, Ted S Jardetzky, Andrea L Chin, David C Johnson, Adam L Vanarsdall

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 3% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Pooled it
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  7. The Pentamer glycoprotein complex inhibits viral Immediate Early transcription during Human Cytomegalovirus infections.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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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

5 authors at 2 institutions in 1 country.

Jing LiuDepartment of Structural Biology, Stanford University School of Medicine, Stanford, California, USA.
Ted S JardetzkyDepartment of Structural Biology, Stanford University School of Medicine, Stanford, California, USA.
Andrea L ChinDepartment of Molecular Microbiology and Immunology, Oregon Health & Science University, Portland, Oregon, USA.
David C JohnsonDepartment of Molecular Microbiology and Immunology, Oregon Health & Science University, Portland, Oregon, USA.
Adam L VanarsdallDepartment of Molecular Microbiology and Immunology, Oregon Health & Science University, Portland, Oregon, USA vanarsda@ohsu.edu.
Oregon Health & Science University · USStanford University · US

Funding

Human cytomegalovirus entry into epithelial and endothelial cellsR01AI081517 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI JOHNSON, DAVID C. · 2009 to 2019
$4.6M
Structure and function of HCMV gHgL complexesR21AI133192 · NIAID · STANFORD UNIVERSITY · PI JARDETZKY, THEODORE S · 2017 to 2018
$432k
Characterization of HCMV entry receptorsR21AI133014 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI VANARSDALL, ADAM L · 2018 to 2019
$424k
NIAID NIH HHS R01 AI081517NIAID NIH HHS R21 AI133014NIAID NIH HHS R21 AI133192
6 · The paper itself

Abstract

Human cytomegalovirus (HCMV) infects a wide variety of human cell types by different entry pathways that involve distinct envelope glycoprotein complexes that include gH/gL, a trimer complex consisting of gHgL/gO, and a pentamer complex consisting of gH/gL/UL128/UL130/UL131. We characterized the effects of soluble forms of these proteins on HCMV entry. Soluble trimer and pentamer blocked entry of HCMV into epithelial and endothelial cells, whereas soluble gH/gL did not. Trimer inhibited HCMV entry into fibroblast cells, but pentamer and gH/gL did not. Both trimer and pentamer bound to the surfaces of fibroblasts and epithelial cells, whereas gH/gL did not bind to either cell type. Cell surface binding of trimer and pentamer did not involve heparin sulfate moieties. The ability of soluble trimer to block entry of HCMV into epithelial cells did not involve platelet-derived growth factor PDGFRα, which has been reported as a trimer receptor for fibroblasts. Soluble trimer reduced the amount of virus particles that could be adsorbed onto the surface of epithelial cells, whereas soluble pentamer had no effect on virus adsorption. However, soluble pentamer reduced the ability of virus particles to exit from early endosomes into the cytoplasm and then travel to the nucleus. These studies support a model in which both the trimer and pentamer are required for HCMV entry into epithelial and endothelial cells, with trimer interacting with cell surface receptors other than PDGFR and pentamer acting later in the entry pathway to promote egress from endosomes.

Indexed as

Virus InternalizationCell MembraneCells, CulturedCytomegalovirusCytomegalovirus InfectionsDNA, ViralEndosomesEpithelial CellsHumansHuman Umbilical Vein Endothelial CellsMembrane GlycoproteinsProtein BindingProtein MultimerizationRetinal Pigment EpitheliumViral Envelope ProteinsDNA, ViralMembrane GlycoproteinsViral Envelope ProteinsHCMV entryHCMV tropismpentamertrimer

Identifiers

PMID30111564
PMCPMC6189492
OpenAlexW2887660674

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.