Evidence map›Paper›PMID 29514899›Full record

ArticleJournal of virology2018

Role of Microvesicles in the Spread of Herpes Simplex Virus 1 in Oligodendrocytic Cells.

Raquel Bello-Morales, Beatriz Praena, Carmen de la Nuez, María Teresa Rejas, Milagros Guerra, Marcos Galán-Ganga, Manuel Izquierdo, Víctor Calvo, Claude Krummenacher, José Antonio López-Guerrero

Open access · hybridAbstract 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 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.6field-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

54 citing papers in PubMed, 73 citations in OpenAlex.

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  13. Extracellular vesicles as tools and targets in therapy for diseases.Signal transduction and targeted therapy · 2024
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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

10 authors at 3 institutions in 2 countries.

Raquel Bello-MoralesUniversidad Autónoma de Madrid, Departamento de Biología Molecular, Cantoblanco, Madrid, Spain angeles.b@uam.es.ORCID https://orcid.org/0000-0002-8526-6590
Beatriz PraenaUniversidad Autónoma de Madrid, Departamento de Biología Molecular, Cantoblanco, Madrid, Spain.
Carmen de la NuezUniversidad Autónoma de Madrid, Departamento de Biología Molecular, Cantoblanco, Madrid, Spain.
María Teresa RejasCentro de Biología Molecular Severo Ochoa, CSIC-UAM, Cantoblanco, Madrid, Spain.
Milagros GuerraCentro de Biología Molecular Severo Ochoa, CSIC-UAM, Cantoblanco, Madrid, Spain.
Marcos Galán-GangaUniversidad Autónoma de Madrid, Facultad de Medicina, Madrid, Spain.
Manuel IzquierdoUniversidad Autónoma de Madrid, Facultad de Medicina, Madrid, Spain.
Víctor CalvoUniversidad Autónoma de Madrid, Facultad de Medicina, Madrid, Spain.
Claude KrummenacherDepartment of Biological Sciences and Department of Molecular and Cellular Biosciences, Rowan University, Glassboro, New Jersey, USA.
José Antonio López-GuerreroUniversidad Autónoma de Madrid, Departamento de Biología Molecular, Cantoblanco, Madrid, Spain.
Centro de Biología Molecular Severo Ochoa · ESUniversidad Autónoma de Madrid · ESRowan University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herpes simplex virus 1 (HSV-1) is a neurotropic pathogen that can infect many types of cells and establishes latent infections in the neurons of sensory ganglia. In some cases, the virus spreads into the central nervous system, causing encephalitis or meningitis. Cells infected with several different types of viruses may secrete microvesicles (MVs) containing viral proteins and RNAs. In some instances, extracellular microvesicles harboring infectious virus have been found. Here we describe the features of shedding microvesicles released by the human oligodendroglial HOG cell line infected with HSV-1 and their participation in the viral cycle. Using transmission electron microscopy, we detected for the first time microvesicles containing HSV-1 virions. Interestingly, the Chinese hamster ovary (CHO) cell line, which is resistant to infection by free HSV-1 virions, was susceptible to HSV-1 infection after being exposed to virus-containing microvesicles. Therefore, our results indicate for the first time that MVs released by infected cells contain virions, are endocytosed by naive cells, and lead to a productive infection. Furthermore, infection of CHO cells was not completely neutralized when virus-containing microvesicles were preincubated with neutralizing anti-HSV-1 antibodies. The lack of complete neutralization and the ability of MVs to infect nectin-1/HVEM-negative CHO-K1 cells suggest a novel way for HSV-1 to spread to and enter target cells. Taken together, our results suggest that HSV-1 could spread through microvesicles to expand its tropism and that microvesicles could shield the virus from neutralizing antibodies as a possible mechanism to escape the host immune response.

Indexed as

AnimalsAntibodies, ViralCell-Derived MicroparticlesCell LineCell MembraneChlorocebus aethiopsCHO CellsCricetulusEndocytosisHeLa CellsHerpes SimplexHerpesvirus 1, HumanHumansMicroscopy, Electron, TransmissionOligodendrogliaVero CellsAntibodies, Viralextracellular vesiclesherpes simplex virusmicrovesiclesoligodendrocytesviral spread

Identifiers

PMID29514899
PMCPMC5923088
OpenAlexW2794346498

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.