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Generation of SARS-CoV-2 reporter replicon for high-throughput antiviral screening and testing.
He, Xi; Quan, Shuo; Xu, Min; Rodriguez, Silveria; Goh, Shih Lin; Wei, Jiajie; Fridman, Arthur; Koeplinger, Kenneth A; Carroll, Steve S; Grobler, Jay A; Espeseth, Amy S; Olsen, David B; Hazuda, Daria J; Wang, Dai.
  • He X; Infectious Disease and Vaccines, Merck and Company, Inc., Kenilworth, NJ 07033.
  • Quan S; Infectious Disease and Vaccines, Merck and Company, Inc., Kenilworth, NJ 07033.
  • Xu M; Infectious Disease and Vaccines, Merck and Company, Inc., Kenilworth, NJ 07033.
  • Rodriguez S; Infectious Disease and Vaccines, Merck and Company, Inc., Kenilworth, NJ 07033.
  • Goh SL; Infectious Disease and Vaccines, Merck and Company, Inc., Kenilworth, NJ 07033.
  • Wei J; Infectious Disease and Vaccines, Merck and Company, Inc., Kenilworth, NJ 07033.
  • Fridman A; Infectious Disease and Vaccines, Merck and Company, Inc., Kenilworth, NJ 07033.
  • Koeplinger KA; Infectious Disease and Vaccines, Merck and Company, Inc., Kenilworth, NJ 07033.
  • Carroll SS; Infectious Disease and Vaccines, Merck and Company, Inc., Kenilworth, NJ 07033.
  • Grobler JA; Infectious Disease and Vaccines, Merck and Company, Inc., Kenilworth, NJ 07033.
  • Espeseth AS; Infectious Disease and Vaccines, Merck and Company, Inc., Kenilworth, NJ 07033.
  • Olsen DB; Infectious Disease and Vaccines, Merck and Company, Inc., Kenilworth, NJ 07033.
  • Hazuda DJ; Infectious Disease and Vaccines, Merck and Company, Inc., Kenilworth, NJ 07033.
  • Wang D; Infectious Disease and Vaccines, Merck and Company, Inc., Kenilworth, NJ 07033 dai_wang@merck.com.
Proc Natl Acad Sci U S A ; 118(15)2021 04 13.
Article in English | MEDLINE | ID: covidwho-1152940
ABSTRACT
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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Replicon / High-Throughput Screening Assays / SARS-CoV-2 / COVID-19 Type of study: Experimental Studies Limits: Animals / Humans Language: English Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Replicon / High-Throughput Screening Assays / SARS-CoV-2 / COVID-19 Type of study: Experimental Studies Limits: Animals / Humans Language: English Year: 2021 Document Type: Article