Evidence map›Paper›PMID 18815310›Full record

ArticleJournal of virology2008

Human cytomegalovirus glycoproteins gB and gH/gL mediate epithelial cell-cell fusion when expressed either in cis or in trans.

Adam L Vanarsdall, Brent J Ryckman, Marie C Chase, David C Johnson

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 114 papers.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed
4.2field-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

114 citing papers in PubMed, 148 citations in OpenAlex.

  1. Trial
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  13. Virus-Induced Cell Fusion and Syncytia Formation.Results and problems in cell differentiation · 2024
    Article
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54 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Adam L VanarsdallDept. of Molecular Microbiology and Immunology, Oregon Health and Science University, 3181 SW Sam Jackson Park Rd., Portland, OR 97239, USA.
Brent J Ryckman
Marie C Chase
David C Johnson
Oregon Health & Science University · US

Funding

INTERACTIONS AT THE MICROBE/HOST INTERFACET32AI007472 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI LANDFEAR, SCOTT M · 1995 to 2019
$6.7M
INHIBITION OF CLASS I ANTIGEN PRESENTATION BY HSV ICP47R01EY011245 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JOHNSON, DAVID C. · 1996 to 2008
$3.6M
Herpes Simplex Virus Transmission Across Cell JunctionsR01AI055051 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI JOHNSON, DAVID C. · 2003 to 2007
$1.5M
Herpes Simplex Virus US9 in Ocular DiseaseF32EY015965 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI RYCKMAN, BRENT J. · 2004 to 2006
$134k
NEI NIH HHS EY11245NEI NIH HHS F32 EY015965NEI NIH HHS F32-EY015965NEI NIH HHS R01 EY011245NIAID NIH HHS AI055051NIAID NIH HHS R01 AI055051NIAID NIH HHS T32 AI007472NIAID NIH HHS T32-AI07472
6 · The paper itself

Abstract

Herpesviruses use a cascade of interactions with different cell surface molecules to gain entry into cells. In many cases, this involves binding to abundant glycosaminoglycans or integrins followed by interactions with more limited cell surface proteins, leading to fusion with cellular membranes. Human cytomegalovirus (HCMV) has the ability to infect a wide variety of human cell types in vivo. However, very little is known about which HCMV glycoproteins mediate entry into various cell types, including relevant epithelial and endothelial cells. For other herpesviruses, studies of cell-cell fusion induced by viral proteins have provided substantial information about late stages of entry. In this report, we describe the fusion of epithelial, endothelial, microglial, and fibroblast cells in which HCMV gB and gH/gL were expressed from nonreplicating adenovirus vectors. Fusion frequently involved the majority of cells, and gB and gH/gL were both necessary and sufficient for fusion, whereas no fusion occurred when either glycoprotein was omitted. Coexpression of UL128, UL130, and UL131 did not enhance fusion. We concluded that the HCMV core fusion machinery consists of gB and gH/gL. Coimmunoprecipitation indicated that HCMV gB and gH/gL can interact. Importantly, expression of gB and gH/gL in trans (gB-expressing cells mixed with other gH/gL-expressing cells) resulted in substantial fusion. We believe that this is the first description of a multicomponent viral fusion machine that can be split between cells. If gB and gH/gL must interact for fusion, then these molecules must reach across the space between apposing cells. Expression of gB and gH/gL in trans with different cell types revealed surface molecules that are required for fusion on HCMV-permissive cells but not on nonpermissive cells.

Indexed as

Cell FusionCell LineEpithelial CellsHumansImmunoprecipitationMembrane GlycoproteinsViral Envelope ProteinsViral Proteinsglycoprotein B, Simplexvirusglycoprotein H, CytomegalovirusMembrane GlycoproteinsUL115 protein, Human herpesvirus 5UL128 protein, human cytomegalovirusViral Envelope ProteinsViral Proteins

Identifiers

PMID18815310
PMCPMC2583677
OpenAlexW2171072908

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.