Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9288364 | Virology | 2005 | 9 Pages |
Abstract
Respiratory syncytial virus (RSV) induces the production of a number of cytokines and chemokines by activation of nuclear factor kappa B (NF-κB). The activation of NF-κB has been shown to depend on viral replication in the infected cells. In this study, we demonstrate that expression of RSV M2-1 protein, a transcriptional processivity and anti-termination factor, is sufficient to activate NF-κB in A549 cells. Electromobility shift assays show increased NF-κB complexes in the nuclei of M2-1-expressing cells. M2-1 protein is found in nuclei of M2-1-expressing cells and in RSV-infected cells. Co-immunoprecipitations of nuclear extracts of M2-1-expressing cells and of RSV-infected cells revealed an association of M2-1 with Rel A protein. Furthermore, the activation of NF-κB depends on the C-terminus of the RSV M2-1 protein, as shown by NF-κB-induced gene expression of a reporter gene construct.
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Authors
Kerstin Reimers, Katja Buchholz, Hermann Werchau,