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J Gen Virol 88 (2007), 1319-1323; DOI 10.1099/vir.0.82526-0

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Short Communication

Human MxA protein confers resistance to double-stranded RNA viruses of two virus families

Egbert Mundt{dagger}

Institute of Molecular Biology, Friedrich-Loeffler-Institut, 17493 Greifswald-Insel Riems, Germany

Correspondence
Egbert Mundt
emundt{at}uga.edu

The interferon-induced human MxA protein belongs to the dynamin superfamily of large GTPases and accumulates in the cytoplasm. MxA is a key component of the innate antiviral response and has previously been shown to inhibit several viruses with single-stranded RNA genomes of both polarities and a DNA virus. In addition, MxA also targets two double-stranded RNA viruses, Infectious bursal disease virus and a mammalian reovirus as shown in this study. Thus, the antiviral spectrum of human MxA is broader than hitherto suspected. Interestingly, virus growth was not affected in cells expressing MxA(E645R), a mutant form of MxA that showed antiviral activity against orthomyxoviruses.

{dagger}Present address: Poultry Diagnostic and Research Center, College of Veterinary Medicine, The University of Georgia, 953 College Station Rd, Athens, GA 30602, USA.




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A. Hoenen, W. Liu, G. Kochs, A. A. Khromykh, and J. M. Mackenzie
West Nile virus-induced cytoplasmic membrane structures provide partial protection against the interferon-induced antiviral MxA protein
J. Gen. Virol., November 1, 2007; 88(11): 3013 - 3017.
[Abstract] [Full Text] [PDF]




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