π The ADP-ribose-1β³-monophosphatase domains of severe acute respiratory syndrome coronavirus and human coronavirus 229E mediate resistance to antiviral interferon responses
Several plus-strand RNA viruses encode proteins containing macrodomains. These domains possess ADP-ribose-1β³-phosphatase (ADRP) activity and/or bind poly(ADP-ribose), poly(A) or poly(G). The relevance of these activities in the viral life cycle has not yet been resolved. Here, we report that genetically engineered mutants of severe acute respiratory syndrome coronavirus (SARS-CoV) and human coronavirus 229E (HCoV-229E) expressing ADRP-deficient macrodomains displayed an increased sensitivity to the antiviral effect of alpha interferon compared with their wild-type counterparts. The data suggest that macrodomain-associated ADRP activities may have a role in viral escape from the innate immune responses of the host. Β© 2011.
keywords
π severe acute (1373)
π syndrome coronavirus (1074)
π life cycle (63)
π innate immune (105)
π human coronavirus (623)
π immune response (314)
π data suggest (146)
π immune responses (142)
π respiratory syndrome (2004)
π acute respiratory (1734)
author
π€ Kuri, Thomas
π€ Eriksson, Klara K.
π€ Putics, Akos
π€ ZΓΌst, Roland
π€ Snijder, Eric J.
π€ Davidson, Andrew D.
π€ Siddell, Stuart G.
π€ Thiel, Volker
π€ Ziebuhr, John
π€ Weber, Friedemann
year
β° 2011
journal
π Journal of General Virology
issn
π 00221317 14652099
volume
92
number
8
page
1899-1905
citedbycount
42
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