Abstract
The Thogoto virus ML protein suppresses interferon synthesis in infected cells. Nevertheless, a virus mutant lacking ML remained highly pathogenic in standard laboratory mice. It was strongly attenuated, however, in mice carrying the interferon-responsive Mx1 gene found in wild mice, demonstrating that enhanced interferon synthesis is protective only if appropriate antiviral effector molecules are present. Our study shows that the virulence-enhancing effects of some viral interferon antagonists may escape detection in conventional animal models.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Animals, Newborn
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Disease Models, Animal
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GTP-Binding Proteins / genetics
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GTP-Binding Proteins / metabolism*
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Interferons / biosynthesis
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Mice
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Mice, Inbred BALB C
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Mutation
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Myxovirus Resistance Proteins
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Orthomyxoviridae Infections / physiopathology*
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Orthomyxoviridae Infections / virology
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Thogotovirus / genetics
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Thogotovirus / pathogenicity*
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Viral Matrix Proteins / genetics
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Viral Matrix Proteins / metabolism*
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Virulence
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Virulence Factors / genetics
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Virulence Factors / metabolism*
Substances
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Mx1 protein, mouse
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Myxovirus Resistance Proteins
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Viral Matrix Proteins
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Virulence Factors
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Interferons
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GTP-Binding Proteins