Abstract |
Human metapneumovirus (hMPV), a leading cause of respiratory tract infections in infants, inhibits type I interferon (IFN) signaling by an unidentified mechanism. In this study, we showed that infection of airway epithelial cells with hMPV decreased cellular level of Janus tyrosine kinase (Jak1) and tyrosine kinase 2 (Tyk2), due to enhanced proteosomal degradation and reduced gene transcription. In addition, hMPV infection also reduced the surface expression of type I IFN receptor (IFNAR). These inhibitory mechanisms are different from the ones employed by respiratory syncytial virus (RSV), which does not affect Jak1, Tyk2 or IFNAR expression, but degrades downstream signal transducer and activator of transcription proteins 2 (STAT2), although both viruses are pneumoviruses belonging to the Paramyxoviridae family. Our study identifies a novel mechanism by which hMPV inhibits STAT1 and 2 activation, ultimately leading to viral evasion of host IFN responses.
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Authors | Junping Ren, Deepthi Kolli, Tianshuang Liu, Renling Xu, Roberto P Garofalo, Antonella Casola, Xiaoyong Bao |
Journal | PloS one
(PLoS One)
Vol. 6
Issue 9
Pg. e24496
( 2011)
ISSN: 1932-6203 [Electronic] United States |
PMID | 21949722
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Protein Subunits
- STAT2 Transcription Factor
- Receptor, Interferon alpha-beta
- Interferon-beta
- Janus Kinase 1
- TYK2 Kinase
- Proteasome Endopeptidase Complex
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Topics |
- Down-Regulation
- Epithelial Cells
(cytology, enzymology, metabolism, virology)
- Humans
- Interferon-beta
(metabolism, pharmacology)
- Janus Kinase 1
(metabolism)
- Metapneumovirus
(physiology)
- Proteasome Endopeptidase Complex
(metabolism)
- Protein Subunits
(metabolism)
- Proteolysis
- Receptor, Interferon alpha-beta
(metabolism)
- STAT2 Transcription Factor
(metabolism)
- Signal Transduction
- TYK2 Kinase
(metabolism)
- Transcription, Genetic
- Virus Replication
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