Skip to content

Advertisement

  • Oral presentation
  • Open Access

The early protective innate immune response against West Nile virus

  • 1,
  • 1,
  • 2,
  • 2,
  • 2 and
  • 1Email author
BMC Proceedings20082 (Suppl 1) :S8

https://doi.org/10.1186/1753-6561-2-s1-s8

  • Published:

Keywords

  • West Nile Virus
  • Interferon Regulatory Factor
  • West Nile Virus Infection
  • Cellular Tropism
  • Specific Host Factor

The type I interferon (IFN)-α/β response plays an essential role in controlling West Nile virus (WNV) tropism, replication and spread to the central nervous system (CNS) in mice. Induction of IFN-α/β relies on the detection of viruses by specific host factors known as pattern-recognition receptors. Central to this signaling pathway are the transcription factors interferon regulatory factors (IRF)-3 and IRF-7, which induce IFN-α/β gene expression. We used IRF-3-/-, IRF-7-/- and IRF-3-/- × IRF-7-/- mice to define how a deficiency of master innate immune response transcriptional factors impacts WNV pathogenesis and IFN signaling responses. Whereas WNV-infected wild type mice exhibited 35% mortality, mice lacking IRF-3 and/or IRF-7 had 100% mortality with enhanced viral burdens in peripheral and CNS organs, with altered tissue and cellular tropism. A deficiency in IRF-3 did not alter the systemic IFN response in vivo or IFN-α/β production ex vivo in immune cells. However, IRF-3 restricted WNV replication in macrophages by regulating basal expression of host defense molecules. Moreover, IRF-3 regulated WNV replication through IFN-dependent mechanisms in neurons. In contrast, an absence of IRF-7 abolished the systemic IFN production in mice and abrogated IFN-α responses in primary cells with little effect on IFN-β induction. Notably, a combined deficiency of IRF-3 and IRF-7 sustained enhanced WNV replication in vivo and in primary cells but did not completely abolish the IFN-b responses. These data show an essential role of IRF-3 and IRF-7 in the early control of WNV infection by regulating not only IFN responses but also antiviral programs in a cell/tissue-specific manner.

Authors’ Affiliations

(1)
Washington University School of Medicine, St Louis, MO, USA
(2)
University of Washington School of Medicine, Seattle, WA, USA

Copyright

© Daffis et al; licensee BioMed Central Ltd. 2008

This article is published under license to BioMed Central Ltd.

Advertisement