Login / Signup

Generation of SARS-CoV-2 reporter replicon for high-throughput antiviral screening and testing.

Xi HeShuo QuanMin XuSilveria RodriguezShih Lin GohJiajie WeiArthur FridmanKenneth A KoeplingerSteve S CarrollJay A GroblerAmy S EspesethDavid B OlsenDaria J HazudaDai Wang
Published in: Proceedings of the National Academy of Sciences of the United States of America (2021)
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) research and antiviral discovery are hampered by the lack of a cell-based virus replication system that can be readily adopted without biosafety level 3 (BSL-3) restrictions. Here, the construction of a noninfectious SARS-CoV-2 reporter replicon and its application in deciphering viral replication mechanisms and evaluating SARS-CoV-2 inhibitors are presented. The replicon genome is replication competent but does not produce progeny virions. Its replication can be inhibited by RdRp mutations or by known SARS-CoV-2 antiviral compounds. Using this system, a high-throughput antiviral assay has also been developed. Significant differences in potencies of several SARS-CoV-2 inhibitors in different cell lines were observed, which highlight the challenges of discovering antivirals capable of inhibiting viral replication in vivo and the importance of testing compounds in multiple cell culture models. The generation of a SARS-CoV-2 replicon provides a powerful platform to expand the global research effort to combat COVID-19.
Keyphrases
  • sars cov
  • respiratory syndrome coronavirus
  • high throughput
  • single cell
  • small molecule
  • stem cells
  • signaling pathway
  • cell therapy
  • dna methylation
  • genome wide