Evidence map›Paper›PMID 23698302›Full record

ArticleJournal of virology2013

Epstein-Barr virus transcytosis through polarized oral epithelial cells.

Sharof M Tugizov, Rossana Herrera, Joel M Palefsky

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
3.3field-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

68 citing papers in PubMed, 92 citations in OpenAlex.

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  11. Tissue and cellular tropism ofVeterinary pathology · 2024
    Article
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  13. Comparative Analysis of the Humoral Immune Response to the EBV Proteome across EBV-Related Malignancies.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2023
    Article
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8 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

3 authors at 1 institution in 1 country.

Sharof M TugizovDepartment of Medicine, University of California San Francisco, San Francisco, California, USA. sharof.tugizov@ucsf.edu
Rossana Herrera
Joel M Palefsky
University of California, San Francisco · US

Funding

Molecular mechanisms of oral HIV transmission modeling MTCTR01DE023315 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI TUGIZOV, SHAROF M · 2013 to 2017
$2.3M
EBV BMRF-2 Protein in Infection of Oral Epithelial CellsR01DE014894 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI TUGIZOV, SHAROF M · 2003 to 2007
$1.5M
HIV transcellular and transsynaptic penetration of mucosal epitheliumR21DE021011 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI TUGIZOV, SHAROF M · 2010 to 2011
$423k
HIV AND EBV INTERACTION IN ORAL MUCOSAL EPITHELIUMR21DE016009 · NIDCR · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI TUGIZOV, SHAROF M · 2004 to 2005
$417k
NIDCR NIH HHS R01 DE014894NIDCR NIH HHS R01 DE023315NIDCR NIH HHS R01 DE14894NIDCR NIH HHS R21 DE016009NIDCR NIH HHS R21 DE021011
6 · The paper itself

Abstract

Although Epstein-Barr virus (EBV) is an orally transmitted virus, viral transmission through the oropharyngeal mucosal epithelium is not well understood. In this study, we investigated how EBV traverses polarized human oral epithelial cells without causing productive infection. We found that EBV may be transcytosed through oral epithelial cells bidirectionally, from both the apical to the basolateral membranes and the basolateral to the apical membranes. Apical to basolateral EBV transcytosis was substantially reduced by amiloride, an inhibitor of macropinocytosis. Electron microscopy showed that virions were surrounded by apical surface protrusions and that virus was present in subapical vesicles. Inactivation of signaling molecules critical for macropinocytosis, including phosphatidylinositol 3-kinases, myosin light-chain kinase, Ras-related C3 botulinum toxin substrate 1, p21-activated kinase 1, ADP-ribosylation factor 6, and cell division control protein 42 homolog, led to significant reduction in EBV apical to basolateral transcytosis. In contrast, basolateral to apical EBV transcytosis was substantially reduced by nystatin, an inhibitor of caveolin-mediated virus entry. Caveolae were detected in the basolateral membranes of polarized human oral epithelial cells, and virions were detected in caveosome-like endosomes. Methyl β-cyclodextrin, an inhibitor of caveola formation, reduced EBV basolateral entry. EBV virions transcytosed in either direction were able to infect B lymphocytes. Together, these data show that EBV transmigrates across oral epithelial cells by (i) apical to basolateral transcytosis, potentially contributing to initial EBV penetration that leads to systemic infection, and (ii) basolateral to apical transcytosis, which may enable EBV secretion into saliva in EBV-infected individuals.

Indexed as

ADP-Ribosylation Factor 6AmilorideAnimalsCallithrixCell LineDNA PrimersFluorescent Antibody TechniqueHerpesvirus 4, HumanHumansImmunoglobulin GKeratinocytesMicroscopy, Electron, TransmissionMouth MucosaNystatinPalatine TonsilPolymerase Chain ReactionADP-Ribosylation Factor 6AmilorideARF6 protein, humanDNA PrimersImmunoglobulin GNystatinRNA, Small Interfering

Identifiers

PMID23698302
PMCPMC3700193
OpenAlexW2116092241

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.