π SARS coronavirus 8b reduces viral replication by down-regulating E via an ubiquitin-independent proteasome pathway
The severe acute respiratory syndrome coronavirus (SARS-CoV) 8b protein, which is not expressed by other known coronaviruses, can down-regulate the envelope (E) protein via a proteasome-dependent pathway. Here, we showed that the down-regulation of E is not dependent on the lysine residues on 8b and the reduction of polyubiquitination of E mutants is not correlated with their down-regulation by 8b, suggesting an ubiquitin-independent proteasome pathway is involved. A time-course study revealed that 8b was expressed at late-stages of SARS-CoV infection. By using Vero E6 cells stably expressing green fluorescence protein-tagged 8b, ectopic expression of 8b was shown to significantly reduce the production of progeny virus and down-regulate E expression. Taken together, these results suggest that 8b negatively modulates virus replication by down-regulating E via an ubiquitin-independent proteasome pathway. Β© 2010 Institut Pasteur.
keywords
π severe acute (1373)
π syndrome coronavirus (1074)
π virus replication (219)
π respiratory syndrome (2004)
π results suggest (206)
π acute respiratory (1734)
author
π€ Keng, Choong Tat
π€ Γ
kerstrΓΆm, Sara
π€ Leung, Cynthia Sau Wai
π€ Poon, Leo L.M.
π€ Peiris, J. S.Malik
π€ Mirazimi, Ali
π€ Tan, Yee Joo
year
β° 2011
journal
π Microbes and Infection
issn
π 1769714X 12864579
volume
13
number
2
page
179-188
citedbycount
6
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