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

Authors :
Dieterle ME
Haslwanter D
Bortz RH 3rd
Wirchnianski AS
Lasso G
Vergnolle O
Abbasi SA
Fels JM
Laudermilch E
Florez C
Mengotto A
Kimmel D
Malonis RJ
Georgiev G
Quiroz J
Barnhill J
Pirofski LA
Daily JP
Dye JM
Lai JR
Herbert AS
Chandran K
Jangra RK
Source :
Cell host & microbe [Cell Host Microbe] 2020 Sep 09; Vol. 28 (3), pp. 486-496.e6. Date of Electronic Publication: 2020 Jul 03.
Publication Year :
2020

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.<br />Competing Interests: Declaration of Interests K.C. is a member of the scientific advisory board of Integrum Scientific, LLC.<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1934-6069
Volume :
28
Issue :
3
Database :
MEDLINE
Journal :
Cell host & microbe
Publication Type :
Academic Journal
Accession number :
32738193
Full Text :
https://doi.org/10.1016/j.chom.2020.06.020