Evidence map›Paper›PMID 34086776›Full record

ArticlePloS one2021

Comparative analysis of neuroinvasion by Japanese encephalitis virulent and vaccine viral strains in an in vitro model of human blood-brain barrier.

Cécile Khou, Marco Aurelio Díaz-Salinas, Anaelle da Costa, Christophe Préhaud, Patricia Jeannin, Philippe V Afonso, Marco Vignuzzi, Monique Lafon, Nathalie Pardigon

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. 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

9 authors at 2 institutions in 1 country.

Cécile KhouUnité de Recherche et d'Expertise Environnement et Risques Infectieux, Groupe Arbovirus, Institut Pasteur, Paris, France.
Marco Aurelio Díaz-SalinasUnité de Recherche et d'Expertise Environnement et Risques Infectieux, Groupe Arbovirus, Institut Pasteur, Paris, France.ORCID 0000-0003-2983-0123
Anaelle da CostaUnité de Neuro-Immunologie Virale, Institut Pasteur, Paris, France.
Christophe PréhaudUnité de Neuro-Immunologie Virale, Institut Pasteur, Paris, France.
Patricia JeanninUnité d'Epidémiologie et Physiopathologie des Virus Oncogènes, Institut Pasteur, CNRS UMR 3569, Paris, France.
Philippe V AfonsoUnité d'Epidémiologie et Physiopathologie des Virus Oncogènes, Institut Pasteur, CNRS UMR 3569, Paris, France.
Marco VignuzziUnité des Populations Virales et Pathogenèse, Institut Pasteur, Paris, France.
Monique LafonUnité de Neuro-Immunologie Virale, Institut Pasteur, Paris, France.ORCID 0000-0002-4423-7996
Nathalie PardigonUnité de Recherche et d'Expertise Environnement et Risques Infectieux, Groupe Arbovirus, Institut Pasteur, Paris, France.ORCID 0000-0003-1973-1631
Institut Pasteur · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Japanese encephalitis virus (JEV) is the major cause of viral encephalitis in South East Asia. It has been suggested that, as a consequence of the inflammatory process during JEV infection, there is disruption of the blood-brain barrier (BBB) tight junctions that in turn allows the virus access to the central nervous system (CNS). However, what happens at early times of JEV contact with the BBB is poorly understood. In the present work, we evaluated the ability of both a virulent and a vaccine strain of JEV (JEV RP9 and SA14-14-2, respectively) to cross an in vitro human BBB model. Using this system, we demonstrated that both JEV RP9 and SA14-14-2 are able to cross the BBB without disrupting it at early times post viral addition. Furthermore, we find that almost 10 times more RP9 infectious particles than SA14-14 cross the model BBB, indicating this BBB model discriminates between the virulent RP9 and the vaccine SA14-14-2 strains of JEV. Beyond contributing to the understanding of early events in JEV neuroinvasion, we demonstrate this in vitro BBB model can be used as a system to study the viral determinants of JEV neuroinvasiveness and the molecular mechanisms by which this flavivirus crosses the BBB during early times of neuroinvasion.

Indexed as

Models, BiologicalBlood-Brain BarrierCell LineEncephalitis, JapaneseEncephalitis Virus, JapaneseEndothelial CellsHumansRNA, ViralVirulenceVirus ReplicationRNA, Viral

Identifiers

PMID34086776
PMCPMC8177624
OpenAlexW3164399286

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.