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TRIM5α Restricts Flavivirus Replication by Targeting the Viral Protease for Proteasomal Degradation.
- Source :
-
Cell reports [Cell Rep] 2019 Jun 11; Vol. 27 (11), pp. 3269-3283.e6. - Publication Year :
- 2019
-
Abstract
- Tripartite motif-containing protein 5α (TRIM5α) is a cellular antiviral restriction factor that prevents early events in retrovirus replication. The activity of TRIM5α is thought to be limited to retroviruses as a result of highly specific interactions with capsid lattices. In contrast to this current understanding, we show that both human and rhesus macaque TRIM5α suppress replication of specific flaviviruses. Multiple viruses in the tick-borne encephalitis complex are sensitive to TRIM5α-dependent restriction, but mosquito-borne flaviviruses, including yellow fever, dengue, and Zika viruses, are resistant. TRIM5α suppresses replication by binding to the viral protease NS2B/3 to promote its K48-linked ubiquitination and proteasomal degradation. Importantly, TRIM5α contributes to the antiviral function of IFN-I against sensitive flaviviruses in human cells. Thus, TRIM5α possesses remarkable plasticity in the recognition of diverse virus families, with the potential to influence human susceptibility to emerging flaviviruses of global concern.<br /> (Published by Elsevier Inc.)
- Subjects :
- Animals
Antiviral Restriction Factors
Cats
Chlorocebus aethiops
Dendritic Cells metabolism
Dendritic Cells virology
Flavivirus pathogenicity
Flavivirus physiology
Flavivirus Infections virology
HEK293 Cells
Humans
Protein Binding
Proteolysis
Substrate Specificity
Ubiquitination
Vero Cells
Flavivirus Infections metabolism
Peptide Hydrolases metabolism
Proteasome Endopeptidase Complex metabolism
Tripartite Motif Proteins metabolism
Ubiquitin-Protein Ligases metabolism
Viral Proteins metabolism
Virus Replication
Subjects
Details
- Language :
- English
- ISSN :
- 2211-1247
- Volume :
- 27
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Cell reports
- Publication Type :
- Academic Journal
- Accession number :
- 31189110
- Full Text :
- https://doi.org/10.1016/j.celrep.2019.05.040