Evidence map›Paper›PMID 30082709›Full record

ArticleScientific reports2018

PLVAP and GKN3 Are Two Critical Host Cell Receptors Which Facilitate Japanese Encephalitis Virus Entry Into Neurons.

Sriparna Mukherjee, Nabonita Sengupta, Ankur Chaudhuri, Irshad Akbar, Noopur Singh, Sibani Chakraborty, Amol Ratnakar Suryawanshi, Arindam Bhattacharyya, Anirban Basu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
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  9. Review
  10. Review
  11. The role of PLVAP in endothelial cells.Cell and tissue research · 2023
    Review
  12. Review
  13. Japanese Encephalitis Virus-Infected Cells.Sub-cellular biochemistry · 2023
    Article
  14. Article
  15. Article
  16. Neuroinflammation in neurodegenerationFrontiers in immunology · 2022
    Review
  17. Article
  18. Review
  19. Article
  20. 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 5 institutions in 1 country.

Sriparna MukherjeeNational Brain Research Centre, Manesar, Haryana, 122052, India.
Nabonita SenguptaNational Brain Research Centre, Manesar, Haryana, 122052, India.
Ankur ChaudhuriWest Bengal State University, North 24 Parganas, Barasat, Kolkata, 700126, India.
Irshad AkbarNational Brain Research Centre, Manesar, Haryana, 122052, India.
Noopur SinghNational Brain Research Centre, Manesar, Haryana, 122052, India.
Sibani ChakrabortyWest Bengal State University, North 24 Parganas, Barasat, Kolkata, 700126, India.
Amol Ratnakar SuryawanshiClinical Proteomics, Institute of Life Sciences, Bhubaneswar, Odisha, 751023, India.ORCID 0000-0001-8519-2467
Arindam BhattacharyyaImmunology Lab, Department of Zoology, University of Calcutta, 35, Ballygunge Circular Road, Kolkata, 700019, India. arindam19@yahoo.com.
Anirban BasuNational Brain Research Centre, Manesar, Haryana, 122052, India. anirban@nbrc.ac.in.ORCID 0000-0002-5200-2054
National Brain Research Centre · INUniversity of Calcutta · INWest Bengal State University · INIndian Institute of Science Bangalore · INInstitute of Life Sciences · IN

Funding

Council of Scientific and Industrial Research (CSIR) 27(0307)/14/EMR-IIDepartment of Biotechnology, Ministry of Science and Technology (DBT) BT/PR22341/MED/122/55/2016Department of Science and Technology, Ministry of Science and Technology (DST) If140074
6 · The paper itself

Abstract

Japanese Encephalitis Virus (JEV), a globally important pathogen, belongs to the family Flaviviridae, is transmitted between vertebrate hosts by mosquitoes, principally by Culex tritaeniorhynchus. The E-glycoprotein of the virus mediates its attachment to the host cell receptors. In this study, we cloned and purified JEV E-glycoprotein in pET28a vector using E. coli BL21 (DE3) cells. A pull down assay was performed using plasma membrane fraction of BALB/c mouse brain and E-glycoprotein as a bait protein. 2-Dimensional Gel Electrophoresis based separation of the interacting proteins was analyzed by mass spectrometry. Among all the identified partners of E-glycoprotein, PLVAP (Plasmalemma vesicle associated protein) and GKN3 (Gastrokine3) showed significant up-regulation in both JEV infected mouse brain and neuro2a cells. In-silico studies also predicted significant interaction of these receptors with E-glycoprotein. Additionally, overexperssion and silencing of these receptors resulted in increase and reduction in viral load respectively, suggesting them as two critical cellular receptors governing JEV entry and propagation in neurons. In support, we observed significant expression of PLVAP but not GKN3 in post-mortem autopsied human brain tissue. Our results establish two novel receptor proteins in neurons in case of JEV infection, thus providing potential targets for antiviral research.

Indexed as

AnimalsBrainCarrier ProteinsCell Line, TumorElectrophoresis, Gel, Two-DimensionalEncephalitis, JapaneseEncephalitis Virus, JapaneseFemaleMaleMass SpectrometryMembrane ProteinsMiceMice, Inbred BALB CNeuronsViral Envelope ProteinsCarrier Proteinsgastrokine 3 protein, mouseMembrane ProteinsPlvap protein, mouseViral Envelope Proteins

Identifiers

PMID30082709
PMCPMC6079088
OpenAlexW2885661907

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.