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Properties of H7N7 influenza A virus strain SC35M lacking interferon antagonist NS1 in mice and chickens

Jürgen Stech^2,

¹ Department of Virology, University of Freiburg, 79104 Freiburg, Germany
² Institute for Virology, University of Marburg, Marburg, Germany
³ Institute for Animal Physiology, University of Munich, Munich, Germany
⁴ Institute of Virology and Immunoprophylaxis, Mittelhäusern, Switzerland
⁵ Institute for Medical Virology, University of Zürich, Zürich, Switzerland

Correspondence
Peter Staeheli
peter.staeheli{at}uniklinik-freiburg.de

Non-structural protein NS1 of influenza A virus counteracts the host immune response by blocking the synthesis of type I interferon (IFN). As deletion of the complete NS1 gene has to date been reported only in the human H1N1 strain A/PR/8/34, it remained unclear whether NS1 is a non-essential virulence factor in other influenza A virus strains as well. In this report, the properties of NS1-deficient mutants derived from strain SC35M (H7N7) are described. A mutant of SC35M that completely lacks the NS1 gene was an excellent inducer of IFN in mammalian and avian cells in culture and, consequently, was able to multiply efficiently only in cell lines with defects in the type I IFN system. Virus mutants carrying C-terminally truncated versions of NS1 were less powerful inducers of IFN and were attenuated less strongly in human A549 cells. Although attenuated in wild-type mice, these mutants remained highly pathogenic for mice lacking the IFN-regulated antiviral factor Mx1. In contrast, the NS1-deficient SC35M mutant was completely non-pathogenic for wild-type mice, but remained pathogenic for mice lacking Mx1 and double-stranded RNA-activated protein kinase (PKR). Wild-type SC35M, but not the NS1-deficient mutant virus, was able to replicate in the upper respiratory tract of birds, but neither virus induced severe disease in adult chickens. Altogether, this study supports the view that NS1 represents a non-essential virulence factor of different influenza A viruses.

Published online ahead of print on 2 February 2007 as DOI 10.1099/vir.0.82764-0.

Present address: Friedrich Loeffler Institute, Federal Research Institute for Animal Health, Greifswald, Germany.

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