๐ Coronavirus nsp10/nsp16 methyltransferase can be targeted by nsp10-derived peptide in vitro and in vivo to reduce replication and pathogenesis
ยฉ 2015, American Society for Microbiology. The 5' cap structures of eukaryotic mRNAs are important for RNA stability and protein translation. Many viruses that replicate in the cytoplasm of eukaryotes have evolved 2'-O-methyltransferases (2'-O-MTase) to autonomously modify their mRNAs and carry a cap-1 structure (m7Gppp. Nm) at the 5' end, thereby facilitating viral replication and escaping innate immune recognition in host cells. Previous studies showed that the 2'-O-MTase activity of severe acute respiratory syndrome coronavirus (SARSCoV) nonstructural protein 16 (nsp16) needs to be activated by nsp10, whereas nsp16 of feline coronavirus (FCoV) alone possesses 2'-O-MTase activity (E. Decroly et al., J Virol 82:8071- 8084, 2008, http://dx.doi.org/10.1128/JVI.00407-08; M. Bouvet et al., PLoS Pathog 6:e1000863, 2010, http://dx.doi.org/10.1371/journal.ppat.1000863; E. Decroly et al., PLoS Pathog 7:e1002059, 2011, http://dx.doi.org/10.1371/journal.ppat.1002059; Y. Chen et al., PLoS Pathog 7:e1002294, 2011, http://dx.doi.org/10.1371 /journal.ppat.1002294). In this study, we demonstrate that stimulation of nsp16 2'-O-MTase activity by nsp10 is a universal and conserved mechanism in coronaviruses, including FCoV, and that nsp10 is functionally interchangeable in the stimulation of nsp16 of different coronaviruses. Based on our current and previous studies, we designed a peptide (TP29) from the sequence of the interaction interface of mouse hepatitis virus (MHV) nsp10 and demonstrated that the peptide inhibits the 2'-O-MTase activity of different coronaviruses in biochemical assays and the viral replication inMHVinfection and SARS-CoV replicon models. Interestingly, the peptide TP29 exerted robust inhibitory effects in vivo in MHV-infected mice by impairingMHVvirulence and pathogenesis through suppressing virus replication and enhancing type I interferon production at an early stage of infection. Therefore, as a proof of principle, the current results indicate that coronavirus 2'-O-MTase activity can be targeted in vitro and in vivo.
keywords
๐ severe acute (1373)
๐ syndrome coronavirus (1074)
๐ hepatitis virus (437)
๐ host cell (262)
๐ mouse hepatitis (371)
๐ innate immune (105)
๐ virus replication (219)
๐ feline coronavirus (148)
๐ respiratory syndrome (2004)
๐ acute respiratory (1734)
๐ results indicate (178)
๐ viral replication (258)
author
๐ค Wang, Yi
๐ค Sun, Ying
๐ค Wu, Andong
๐ค Xu, Shan
๐ค Pan, Ruangang
๐ค Zeng, Cong
๐ค Jin, Xu
๐ค Ge, Xingyi
๐ค Shi, Zhengli
๐ค Ahola, Tero
๐ค Chen, Yu
๐ค Guo, Deyin
year
โฐ 2015
journal
๐ Journal of Virology
issn
๐ 10985514 0022538X
volume
89
number
16
page
8416-8427
citedbycount
12
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