Abstract
Severe human disease caused by the emerging H7N9 influenza virus in China warrants a rapid response. Here, we present a recombinant Newcastle disease virus expressing a North American lineage H7 influenza virus hemagglutinin. Sera from immunized mice were cross-reactive to a broad range of H7 subtype viruses and inhibited hemagglutination by the novel H7 hemagglutinin. Immunized mice were protected against a heterologous H7 subtype challenge, and genetic analysis suggested that cross-protective antibodies recognize conserved antigenic sites.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Antibodies, Viral / immunology*
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Blotting, Western
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China
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Cluster Analysis
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Communicable Diseases, Emerging / immunology*
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Communicable Diseases, Emerging / prevention & control
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Conserved Sequence / immunology
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Cross Reactions / immunology*
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Enzyme-Linked Immunosorbent Assay
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Genetic Vectors / genetics
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Hemagglutinin Glycoproteins, Influenza Virus / genetics
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Hemagglutinin Glycoproteins, Influenza Virus / immunology*
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Humans
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Immune Sera / immunology
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Influenza A virus / genetics
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Influenza A virus / immunology*
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Mice
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Models, Genetic
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Newcastle disease virus / immunology*
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Newcastle disease virus / metabolism
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Orthomyxoviridae Infections / immunology*
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Orthomyxoviridae Infections / prevention & control
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Phylogeny
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Reverse Genetics / methods
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Viral Vaccines / immunology
Substances
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Antibodies, Viral
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Hemagglutinin Glycoproteins, Influenza Virus
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Immune Sera
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Viral Vaccines
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hemagglutinin, avian influenza A virus