Evidence map›Paper›PMID 32252443›Full record

ArticleViruses2020

Differences in Tissue and Species Tropism of Reptarenavirus Species Studied by Vesicular Stomatitis Virus Pseudotypes.

Yegor Korzyukov, Rommel Iheozor-Ejiofor, Lev Levanov, Teemu Smura, Udo Hetzel, Leonora Szirovicza, Juan Carlos de la Torre, Luis Martinez-Sobrido, Anja Kipar, Olli Vapalahti and 1 more

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  6. Experimental Reptarenavirus Infection ofJournal of virology · 2021
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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

11 authors at 3 institutions in 3 countries.

Yegor KorzyukovMedicum, Department of Virology, University of Helsinki, 00100 Helsinki, Finland.
Rommel Iheozor-EjioforMedicum, Department of Virology, University of Helsinki, 00100 Helsinki, Finland.
Lev LevanovMedicum, Department of Virology, University of Helsinki, 00100 Helsinki, Finland.
Teemu SmuraMedicum, Department of Virology, University of Helsinki, 00100 Helsinki, Finland.
Udo HetzelVetsuisse Faculty, Institute of Veterinary Pathology, University of Zürich, 8006 Zürich, Switzerland.
Leonora SziroviczaMedicum, Department of Virology, University of Helsinki, 00100 Helsinki, Finland.
Juan Carlos de la TorreDepartment of Immunology and Microbial Science IMM-6, The Scripps Research Institute, La Jolla, CA 92037, USA.
Luis Martinez-SobridoTexas Biomedical Research Institute, San Antonio, TX 78227, USA.
Anja KiparVetsuisse Faculty, Institute of Veterinary Pathology, University of Zürich, 8006 Zürich, Switzerland.
Olli VapalahtiMedicum, Department of Virology, University of Helsinki, 00100 Helsinki, Finland.
Jussi HepojokiMedicum, Department of Virology, University of Helsinki, 00100 Helsinki, Finland.
University of Helsinki · FIScripps Research Institute · USTexas Biomedical Research Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reptarenaviruses cause Boid Inclusion Body Disease (BIBD), and co-infections by several reptarenaviruses are common in affected snakes. Reptarenaviruses have only been found in captive snakes, and their reservoir hosts remain unknown. In affected animals, reptarenaviruses appear to replicate in most cell types, but their complete host range, as well as tissue and cell tropism are unknown. As with other enveloped viruses, the glycoproteins (GPs) present on the virion's surface mediate reptarenavirus cell entry, and therefore, the GPs play a critical role in the virus cell and tissue tropism. Herein, we employed single cycle replication, GP deficient, recombinant vesicular stomatitis virus (VSV) expressing the enhanced green fluorescent protein (scrVSV∆G-eGFP) pseudotyped with different reptarenavirus GPs to study the virus cell tropism. We found that scrVSV∆G-eGFPs pseudotyped with reptarenavirus GPs readily entered mammalian cell lines, and some mammalian cell lines exhibited higher, compared to snake cell lines, susceptibility to reptarenavirus GP-mediated infection. Mammarenavirus GPs used as controls also mediated efficient entry into several snake cell lines. Our results confirm an important role of the virus surface GP in reptarenavirus cell tropism and that mamma-and reptarenaviruses exhibit high cross-species transmission potential.

Indexed as

Viral Envelope ProteinsViral TropismA549 CellsAnimalsArenaviridaeCell LineChlorocebus aethiopsGreen Fluorescent ProteinsHEK293 CellsHumansSnakesVero CellsVesiculovirusenhanced green fluorescent proteinGreen Fluorescent ProteinsViral Envelope ProteinsarenavirusBIBDpseudotypereptarenavirustissue tropismVSV

Identifiers

PMID32252443
PMCPMC7232232
OpenAlexW3014680653

What OpenQuestion holds

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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.