Replication and single-cycle delivery of SARS-CoV-2 replicons.
Options
BORIS DOI
Date of Publication
November 26, 2021
Publication Type
Article
Author
Ricardo-Lax, Inna | |
Luna, Joseph M | |
Le Pen, Jérémie | |
Yu, Yingpu | |
Hoffmann, H-Heinrich | |
Schneider, William M | |
Razooky, Brandon S | |
Fernandez-Martinez, Javier | |
Schmidt, Fabian | |
Weisblum, Yiska | |
Schmied, Kimberly | |
Michailidis, Eleftherios | |
Peace, Avery | |
Sánchez-Rivera, Francisco J | |
Lowe, Scott W | |
Rout, Michael P | |
Hatziioannou, Theodora | |
Bieniasz, Paul D | |
Poirier, John T | |
MacDonald, Margaret R | |
Rice, Charles M |
Series
Science
ISSN or ISBN (if monograph)
0036-8075
Publisher
American Association for the Advancement of Science
Language
English
Publisher DOI
PubMed ID
34648371
Description
Molecular virology tools are critical for basic studies of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and for developing new therapeutics. Experimental systems that do not rely on viruses capable of spread are needed for potential use in lower-containment settings. In this work, we use a yeast-based reverse genetics system to develop spike-deleted SARS-CoV-2 self-replicating RNAs. These noninfectious self-replicating RNAs, or replicons, can be trans-complemented with viral glycoproteins to generate replicon delivery particles for single-cycle delivery into a range of cell types. This SARS-CoV-2 replicon system represents a convenient and versatile platform for antiviral drug screening, neutralization assays, host factor validation, and viral variant characterization.
File(s)
File | File Type | Format | Size | License | Publisher/Copright statement | Content | |
---|---|---|---|---|---|---|---|
Thiel_Replication_and_single-cycle_delivery_science.abj8430.pdf | text | Adobe PDF | 1.17 MB | published |