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  1. Article ; Online: Receptor specificity of the influenza virus hemagglutinin modulates sensitivity to soluble collectins of the innate immune system and virulence in mice.

    Tate, Michelle D / Brooks, Andrew G / Reading, Patrick C

    Virology

    2011  Volume 413, Issue 1, Page(s) 128–138

    Abstract: The hemagglutinin (HA) glycoprotein of influenza virus binds to cell surface sialic acid (SA ... viruses is a critical determinant of virulence in a mouse model of influenza infection. ... from the lungs of virus-infected mice that had been depleted of airway macrophages. Sequence analysis identified ...

    Abstract The hemagglutinin (HA) glycoprotein of influenza virus binds to cell surface sialic acid (SA) to initiate infection. In this study, a mutant of influenza A virus strain BJx109 (H3N2) was plaque-purified from the lungs of virus-infected mice that had been depleted of airway macrophages. Sequence analysis identified a single amino acid substitution (S186I) in the vicinity of the receptor-binding site of HA. This substitution was associated with enhanced binding to α(2,3)-Gal-linked SA and an increased ability to infect murine airway epithelial cells. Mutant viruses were less sensitive to neutralization by mouse airway fluids and less efficient in their ability to infect murine macrophages. Moreover, infection of mice with viruses bearing the S186I substitution led to severe disease, characterized by enhanced virus replication, lung pathology and pulmonary edema. Together, these studies confirm that residue 186 of H3 subtype viruses is a critical determinant of virulence in a mouse model of influenza infection.
    MeSH term(s) Amino Acid Substitution ; Animals ; Cell Line ; Collectins/immunology ; Hemagglutinin Glycoproteins, Influenza Virus/chemistry ; Hemagglutinin Glycoproteins, Influenza Virus/genetics ; Hemagglutinin Glycoproteins, Influenza Virus/metabolism ; Humans ; Immune System/immunology ; Influenza A Virus, H3N2 Subtype/chemistry ; Influenza A Virus, H3N2 Subtype/genetics ; Influenza A Virus, H3N2 Subtype/metabolism ; Influenza A Virus, H3N2 Subtype/pathogenicity ; Influenza, Human/immunology ; Influenza, Human/metabolism ; Influenza, Human/pathology ; Influenza, Human/virology ; Lung/pathology ; Lung/virology ; Male ; Mice ; Mice, Inbred C57BL ; N-Acetylneuraminic Acid/metabolism ; Protein Binding ; Receptors, Virus/metabolism ; Species Specificity ; Virulence
    Chemical Substances Collectins ; Hemagglutinin Glycoproteins, Influenza Virus ; Receptors, Virus ; N-Acetylneuraminic Acid (GZP2782OP0)
    Language English
    Publishing date 2011-04-25
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 200425-2
    ISSN 1096-0341 ; 0042-6822
    ISSN (online) 1096-0341
    ISSN 0042-6822
    DOI 10.1016/j.virol.2011.01.035
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Receptor specificity of the influenza virus hemagglutinin modulates sensitivity to soluble collectins of the innate immune system and virulence in mice

    Tate, Michelle D / Brooks, Andrew G / Reading, Patrick C

    Virology. 2011 Apr. 25, v. 413, no. 1

    2011  

    Abstract: The hemagglutinin (HA) glycoprotein of influenza virus binds to cell surface sialic acid (SA ... viruses is a critical determinant of virulence in a mouse model of influenza infection. ... from the lungs of virus-infected mice that had been depleted of airway macrophages. Sequence analysis identified ...

    Abstract The hemagglutinin (HA) glycoprotein of influenza virus binds to cell surface sialic acid (SA) to initiate infection. In this study, a mutant of influenza A virus strain BJx109 (H3N2) was plaque-purified from the lungs of virus-infected mice that had been depleted of airway macrophages. Sequence analysis identified a single amino acid substitution (S186I) in the vicinity of the receptor-binding site of HA. This substitution was associated with enhanced binding to α(2,3)-Gal-linked SA and an increased ability to infect murine airway epithelial cells. Mutant viruses were less sensitive to neutralization by mouse airway fluids and less efficient in their ability to infect murine macrophages. Moreover, infection of mice with viruses bearing the S186I substitution led to severe disease, characterized by enhanced virus replication, lung pathology and pulmonary edema. Together, these studies confirm that residue 186 of H3 subtype viruses is a critical determinant of virulence in a mouse model of influenza infection.
    Keywords Orthomyxoviridae ; amino acid substitution ; animal models ; edema ; epithelial cells ; glycoproteins ; hemagglutinins ; influenza ; innate immunity ; lungs ; macrophages ; mice ; mutants ; neutralization ; sequence analysis ; sialic acids ; virulence ; virus replication ; viruses
    Language English
    Dates of publication 2011-0425
    Size p. 128-138.
    Publishing place Elsevier Inc.
    Document type Article
    ZDB-ID 200425-2
    ISSN 1096-0341 ; 0042-6822
    ISSN (online) 1096-0341
    ISSN 0042-6822
    DOI 10.1016/j.virol.2011.01.035
    Database NAL-Catalogue (AGRICOLA)

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