4.3 Article

Sabotage of antiviral signaling and effectors by influenza viruses

Journal

BIOLOGICAL CHEMISTRY
Volume 389, Issue 10, Pages 1299-1305

Publisher

WALTER DE GRUYTER GMBH
DOI: 10.1515/BC.2008.146

Keywords

influenza virus; innate immunity; interferon; NS1 protein; RIG-I; signaling

Funding

  1. Deutsche Forschungsgemeinschaft [Wo 554/3-2]
  2. German Ministry of Health
  3. European Union (Flusecure, FluVacc and Euroflu).

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Vertebrate cells activate multiple signaling modules upon virus infection to eliminate the invading pathogen and to prevent the establishment of a persistent infection. A major immediate response pathway is controlled by the RNA helicases RIG-I and MDA5, which, after recognition of viral nucleic acids, signal induction of the interferon (IFN)-alpha/beta cytokine family that upregulates numerous antiviral effector proteins. Virulent viruses, in contrast, have learned during co-evolution with their hosts to manipulate or avoid this response in order to prevail in a repulsive environment. Focusing on the influenza viruses and their IFN-antagonistic NS1 proteins, we summarize recent progress in this rapidly evolving field at the intersection of virology and immunobiology involving studies of how viral pathogens induce and sabotage cellular defenses.

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