๐ Coronavirus protein processing and RNA synthesis is inhibited by the cysteine proteinase inhibitor E64d
Mouse hepatitis virus strain A59 (MHV-A59) encodes within the 22-kb gene 1 a large polyprotein containing three proteinase domains with proven or predicted cysteine catalytic residues E64d, a specific, irreversible inhibitor of cysteine (thiol) proteinases, inhibits the processing of the gene 1 polyprotein. Specifically, E64d blocks the carboxy-terminal cleavage of p65. E64d also inhibits replication of MHV-A59 in routine DBT cells in a dose-dependent manner, resulting in reduced virus titers and viral syncytia formation. This inhibition of replication is associated with a rapid shutoff of new viral RNA synthesis, in a manner similar to that seen in the presence of cycloheximide. The E64d-associated inhibition of RNA synthesis likely results from E64d-specific inhibition of processing of the gene 1 polyprotein, resulting in inactive proteinase or replicase proteins. These results indicate that processing of the MHV-A59 gene 1-encoded polyprotein is required throughout infection to sustain RNA synthesis and virus replication. ยฉ 1995 Academic Press, Inc.
keywords
๐ dose-dependent manner (15)
๐ hepatitis virus (437)
๐ virus replication (219)
๐ virus strain (138)
๐ results indicate (178)
author
๐ค Kim, James C.
๐ค Spence, Robert A.
๐ค Currier, Paul F.
๐ค Lu, Xiaotao
๐ค Denison, Mark R.
year
โฐ 1995
journal
๐ Virology
issn
๐ 00426822
volume
208
number
1
page
1-8
citedbycount
72
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