Evidence map›Paper›PMID 32738193›Full record

ArticleCell host & microbe2020

A Replication-Competent Vesicular Stomatitis Virus for Studies of SARS-CoV-2 Spike-Mediated Cell Entry and Its Inhibition.

M Eugenia Dieterle, Denise Haslwanter, Robert H Bortz, Ariel S Wirchnianski, Gorka Lasso, Olivia Vergnolle, Shawn A Abbasi, J Maximilian Fels, Ethan Laudermilch, Catalina Florez and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell host & microbe, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 164 papers.

0numbers the graph read from it
0cells of the map it votes in
164citing papers in PubMed
4.7field-weighted citation impact, top 3% 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

164 citing papers in PubMed, 239 citations in OpenAlex.

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  6. Viral syncytia evolve to resist interferon.Nature communications · 2026
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104 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 3 institutions in 1 country.

M Eugenia DieterleDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Denise HaslwanterDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Robert H BortzDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Ariel S WirchnianskiDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Gorka LassoDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Olivia VergnolleDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Shawn A AbbasiU.S. Army Medical Research Institute of Infectious Diseases, Frederick, MD 21702, USA.
J Maximilian FelsDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Ethan LaudermilchDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Catalina FlorezDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Chemistry and Life Science, United States Military Academy at West Point, West Point, NY 10996, USA.
Amanda MengottoDivision of Infectious Diseases, Department of Medicine, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, NY 10461, USA.
Duncan KimmelDivision of Infectious Diseases, Department of Medicine, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, NY 10461, USA.
Ryan J MalonisDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
George GeorgievDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Jose QuirozDivision of Infectious Diseases, Department of Medicine, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, NY 10461, USA.
Jason BarnhillDepartment of Chemistry and Life Science, United States Military Academy at West Point, West Point, NY 10996, USA.
Liise-Anne PirofskiDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Division of Infectious Diseases, Department of Medicine, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, NY 10461, USA.
Johanna P DailyDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Division of Infectious Diseases, Department of Medicine, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, NY 10461, USA.
John M DyeU.S. Army Medical Research Institute of Infectious Diseases, Frederick, MD 21702, USA.
Jonathan R LaiDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Andrew S HerbertU.S. Army Medical Research Institute of Infectious Diseases, Frederick, MD 21702, USA; The Geneva Foundation, 917 Pacific Avenue, Tacoma, WA 98402, USA. Electronic address: andrew.s.herbert4.ctr@mail.mil.
Kartik ChandranDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA. Electronic address: kartik.chandran@einsteinmed.org.
Rohit K JangraDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA. Electronic address: rohit.jangra@einsteinmed.org.
Albert Einstein College of Medicine · USUnited States Army Medical Research Institute of Infectious Diseases · USUnited States Military Academy · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007288 · NIGMS · YESHIVA UNIVERSITY · PI AKABAS, MYLES H. · 1985 to 2022
$35.6M
Prometheus: A Platform for Rapid Development of Human Antibody-based Therapeutics and Prophylactics against Emerging Viral ThreatsU19AI142777 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI CHANDRAN, KARTIK · 2019 to 2023
$21.9M
Dissecting the receptor-mediated infection mechanisms of hantavirusesR01AI132633 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI CHANDRAN, KARTIK · 2017 to 2021
$3.2M
Antibodies, B cells and resistance to human cryptococcosisR01AI143453 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI PIROFSKI, LIISE-ANNE · 2019 to 2024
$3.2M
Engineered, multispecific antibodies as broad anti-filovirus therapeuticsR01AI125462 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI LAI, JONATHAN R. · 2017 to 2020
$3.0M
Antibody therapy for pneumococcal diseaseR01AI123654 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI PIROFSKI, LIISE-ANNE · 2017 to 2021
$2.1M
Plasmodium phospholipase A2s as potential novel drug targetsR21AI141367 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI DAILY, JOHANNA PATRICIA · 2019 to 2020
$459k
Discovery & characterization of human monoclonal antibodies targeting multiple arthritogenic alphavirusesF30AI150055 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI MALONIS, RYAN J · 2020 to 2022
$150k
NIAID NIH HHS F30 AI150055NIAID NIH HHS R01 AI123654NIAID NIH HHS R01 AI125462NIAID NIH HHS R01 AI132633NIAID NIH HHS R01 AI143453NIAID NIH HHS R21 AI141367NIAID NIH HHS U19 AI142777NIGMS NIH HHS T32 GM007288
6 · The paper itself

Abstract

There is an urgent need for vaccines and therapeutics to prevent and treat COVID-19. Rapid SARS-CoV-2 countermeasure development is contingent on the availability of robust, scalable, and readily deployable surrogate viral assays to screen antiviral humoral responses, define correlates of immune protection, and down-select candidate antivirals. Here, we generate a highly infectious recombinant vesicular stomatitis virus (VSV) bearing the SARS-CoV-2 spike glycoprotein S as its sole entry glycoprotein and show that this recombinant virus, rVSV-SARS-CoV-2 S, closely resembles SARS-CoV-2 in its entry-related properties. The neutralizing activities of a large panel of COVID-19 convalescent sera can be assessed in a high-throughput fluorescent reporter assay with rVSV-SARS-CoV-2 S, and neutralization of rVSV-SARS-CoV-2 S and authentic SARS-CoV-2 by spike-specific antibodies in these antisera is highly correlated. Our findings underscore the utility of rVSV-SARS-CoV-2 S for the development of spike-specific therapeutics and for mechanistic studies of viral entry and its inhibition.

Indexed as

Angiotensin-Converting Enzyme 2AnimalsAntiviral AgentsBetacoronavirusCell LineChlorocebus aethiopsCoronavirus InfectionsCOVID-19COVID-19 Drug TreatmentCOVID-19 VaccinesDrug Evaluation, PreclinicalHost Microbial InteractionsHumansMutationNeutralization TestsPandemicsACE2 protein, humanAngiotensin-Converting Enzyme 2Antiviral AgentsCOVID-19 VaccinesPeptidyl-Dipeptidase AReceptors, VirusSerine EndopeptidasesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2TMPRSS2 protein, humanViral VaccinesACE2antiviral drugsconvalescent plasmaCOVID-19neutralization assayneutralizing antibodySARS-CoV-2serologysurrogateVSV

Identifiers

PMID32738193
PMCPMC7332447
OpenAlexW3039409489

What OpenQuestion holds

Textmetadata
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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.