Evidence map›Paper›PMID 35491102›Full record

ArticleCell structure and function2022

A method for the generation of pseudovirus particles bearing SARS coronavirus spike protein in high yields.

Yoichiro Fujioka, Sayaka Kashiwagi, Aiko Yoshida, Aya O Satoh, Mari Fujioka, Maho Amano, Yohei Yamauchi, Yusuke Ohba

Open access · goldAbstract read
In one paragraph

Article in Cell structure and function, 2022. 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
0.9field-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, 10 citations in OpenAlex.

  1. SARS-CoV-2 uptake and inflammatory response in senescent endothelial cells are regulated by the BSG/VEGFR2 pathway.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Review
  3. Article
  4. Article
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

8 authors at 4 institutions in 3 countries.

Yoichiro FujiokaDepartment of Cell Physiology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University.
Sayaka KashiwagiDepartment of Cell Physiology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University.
Aiko YoshidaDepartment of Cell Physiology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University.
Aya O SatohDepartment of Cell Physiology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University.
Mari FujiokaDepartment of Cell Physiology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University.
Maho AmanoDepartment of Cell Physiology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University.
Yohei YamauchiAMED-CREST, Japan Agency for Medical Research and Development.
Yusuke OhbaDepartment of Cell Physiology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University.
Hokkaido University · JPJapan Agency for Medical Research and Development · JPBioSurfaces (United States) · USUniversity of Bristol · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ongoing severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has threatened human health and the global economy. Development of additional vaccines and therapeutics is urgently required, but such development with live virus must be conducted with biosafety level 3 confinement. Pseudotyped viruses have been widely adopted for studies of virus entry and pharmaceutical development to overcome this restriction. Here we describe a modified protocol to generate vesicular stomatitis virus (VSV) pseudotyped with SARS-CoV or SARS-CoV-2 spike protein in high yield. We found that a large proportion of pseudovirions produced with the conventional transient expression system lacked coronavirus spike protein at their surface as a result of inhibition of parental VSV infection by overexpression of this protein. Establishment of stable cell lines with an optimal expression level of coronavirus spike protein allowed the efficient production of progeny pseudoviruses decorated with spike protein. This improved VSV pseudovirus production method should facilitate studies of coronavirus entry and development of antiviral agents.Key words: severe acute respiratory syndrome coronavirus (SARS-CoV), SARS-CoV-2, pseudovirus, vesicular stomatitis virus (VSV), spike protein.

Indexed as

Spike Glycoprotein, CoronavirusVesicular stomatitis Indiana virusSARS-CoV-2Spike Glycoprotein, Coronavirusspike protein, SARS-CoV-2pseudovirusSARS-CoV-2severe acute respiratory syndrome coronavirus (SARS-CoV)spike proteinvesicular stomatitis virus (VSV)

Identifiers

PMID35491102
PMCPMC10511058
OpenAlexW4225302717

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.