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Antiviral activity of interferon-λ in chickens

tetano

Editor, Senior Moderator
J Virol. 2013 Dec 26. [Epub ahead of print]
Antiviral activity of interferon-λ in chickens.
Reuter A, Soubies S, H?rtle S, Schusser B, Kaspers B, Staeheli P, Rubbenstroth D.
Author information
Abstract

Interferons (IFNs) are essential components of the antiviral defense system of vertebrates. In mammals, functional receptors for type III IFN (IFN-λ) are mainly found on epithelial cells and IFN-λ was demonstrated to play a crucial role in limiting viral infections of mucosal surfaces. To determine whether IFN-λ plays a similar role in birds, we produced recombinant chicken IFN-λ (chIFN-λ) and we used the replication-competent retroviral RCAS vector system to generate mosaic-transgenic chicken embryos that constitutively express chIFN-λ. We could demonstrate that chIFN-λ markedly inhibited replication of various virus strains, including highly pathogenic influenza A viruses, in ovo and in vivo, as well as in epithelium-rich tissue and cell culture systems. In contrast, chicken fibroblasts responded poorly to chIFN-λ. When applied in vivo to three-week-old chickens, recombinant chIFN-λ strongly induced the IFN-responsive Mx gene in epithelium-rich organs such as lung, trachea and intestinal tract. Correspondingly, these organs were found to express high transcript levels of the putative chIFN-λ receptor alpha chain (chIL28RA) gene. Transfection of chicken fibroblasts with a chIL28RA expression construct rendered these cells responsive to chIFN-λ treatment, indicating that receptor expression determines cell type specificity of IFN-λ action in chickens. Surprisingly, mosaic-transgenic chickens perished soon after hatching, demonstrating a detrimental effect of constitutive chIFN-λ expression. Our data highlight fundamental similarities between the IFN-λ systems of mammals and birds, and suggest that type III IFN might play a role in defending mucosal surfaces against viral intruders in most if not all vertebrates.

PMID:
24371053
[PubMed - as supplied by publisher]

http://www.ncbi.nlm.nih.gov/pubmed/24371053
 
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