The Leader Protein of Theiler's Virus Prevents the Activation of PKR
Author(s) -
Fabian Borghese,
Frédéric Sorgeloos,
Teresa Cesaro,
Thomas Michiels
Publication year - 2019
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.01010-19
Subject(s) - protein kinase r , biology , stress granule , eif 2 kinase , protein kinase a , microbiology and biotechnology , activator (genetics) , protein biosynthesis , virus , rna , innate immune system , kinase , interferon , virology , mitogen activated protein kinase kinase , translation (biology) , immune system , messenger rna , cyclin dependent kinase 2 , biochemistry , gene , genetics
The leader (L) protein encoded by cardioviruses is a very short multifunctional protein that contributes to evasion of the host innate immune response. This protein notably prevents the formation of stress granules in infected cells. Using Theiler’s virus as a model, we show that L proteins can act at two levels in the stress response pathway leading to stress granule formation, the most striking one being the inhibition of eucaryotic translation initiation factor 2 alpha kinase 2 (PKR) activation. Interestingly, the leader protein appears to inhibit PKR via a novel mechanism by rendering this kinase unable to detect double-stranded RNA, its typical activator. Unlike other viral proteins, such as influenza virus NS1, the leader protein appears to interact with neither PKR nor double-stranded RNA, suggesting that it acts indirectly to trigger the inhibition of the kinase.
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