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  1. Article: Filamentous influenza A virus infection predisposes mice to fatal septicemia following superinfection with Streptococcus pneumoniae serotype 3.

    Speshock, Janice L / Doyon-Reale, Nicole / Rabah, R / Neely, Melody N / Roberts, Paul C

    Infection and immunity

    2007  Volume 75, Issue 6, Page(s) 3102–3111

    Abstract: ... pneumoniae serotype 3. S. pneumoniae superinfection results in rapid dissemination of the bacterium ... from the respiratory tract and systemic spread to all major organs of the mice, resulting in fatal septicemia ... self-limiting influenza virus infection is followed by mild, self-limiting superinfection with S ...

    Abstract Previous studies have demonstrated that animals exposed to Streptococcus pneumoniae while recovering from influenza A virus infection exhibit exacerbated disease symptoms. However, many of the current animal models exploring dual viral and bacterial synergistic exacerbations of respiratory disease have utilized mouse-adapted influenza virus and strains of Streptococcus pneumoniae that in themselves are highly lethal to mice. Here we describe a mouse model of bacterial superinfection in which a mild, self-limiting influenza virus infection is followed by mild, self-limiting superinfection with S. pneumoniae serotype 3. S. pneumoniae superinfection results in rapid dissemination of the bacterium from the respiratory tract and systemic spread to all major organs of the mice, resulting in fatal septicemia. This phenomenon in mice was observed in superinfected animals undergoing an active viral infection as well as in mice that had completely cleared the virus 7 to 8 days prior to superinfection. Neutrophils were the predominant cellular inflammatory infiltrate in the lungs of superinfected mice compared to singly infected animals. Among other cytokines and chemokines, the neutrophil activator granulocyte colony-stimulating factor (G-CSF) was found to be significantly overexpressed in the spleens, lungs, and brains of superinfected animals. High G-CSF protein levels were observed in sera and lung lavage fluid from superinfected animals, suggesting that G-CSF is a major contributor to synergistic exacerbation of disease leading to fatal septicemia.
    MeSH term(s) Animals ; Disease Models, Animal ; Disease Susceptibility ; Granulocyte-Macrophage Colony-Stimulating Factor ; Humans ; Influenza A virus/immunology ; Influenza, Human/complications ; Influenza, Human/immunology ; Mice ; Mice, Inbred BALB C ; Orthomyxoviridae Infections/complications ; Pneumococcal Infections/etiology ; Pneumococcal Infections/immunology ; Pneumococcal Infections/microbiology ; Pneumococcal Infections/mortality ; Sepsis/etiology ; Sepsis/mortality ; Streptococcus pneumoniae/immunology ; Superinfection/microbiology ; Superinfection/pathology
    Chemical Substances Granulocyte-Macrophage Colony-Stimulating Factor (83869-56-1)
    Language English
    Publishing date 2007-06
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 218698-6
    ISSN 1098-5522 ; 0019-9567
    ISSN (online) 1098-5522
    ISSN 0019-9567
    DOI 10.1128/IAI.01943-06
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Filamentous Influenza A Virus Infection Predisposes Mice to Fatal Septicemia following Superinfection with Streptococcus pneumoniae Serotype 3

    Speshock, Janice L / Doyon-Reale, Nicole / Rabah, R / Neely, Melody N / Roberts, Paul C

    Infection and immunity. 2007 June, v. 75, no. 6

    2007  

    Abstract: ... pneumoniae serotype 3. S. pneumoniae superinfection results in rapid dissemination of the bacterium ... from the respiratory tract and systemic spread to all major organs of the mice, resulting in fatal septicemia ... self-limiting influenza virus infection is followed by mild, self-limiting superinfection with S ...

    Abstract Previous studies have demonstrated that animals exposed to Streptococcus pneumoniae while recovering from influenza A virus infection exhibit exacerbated disease symptoms. However, many of the current animal models exploring dual viral and bacterial synergistic exacerbations of respiratory disease have utilized mouse-adapted influenza virus and strains of Streptococcus pneumoniae that in themselves are highly lethal to mice. Here we describe a mouse model of bacterial superinfection in which a mild, self-limiting influenza virus infection is followed by mild, self-limiting superinfection with S. pneumoniae serotype 3. S. pneumoniae superinfection results in rapid dissemination of the bacterium from the respiratory tract and systemic spread to all major organs of the mice, resulting in fatal septicemia. This phenomenon in mice was observed in superinfected animals undergoing an active viral infection as well as in mice that had completely cleared the virus 7 to 8 days prior to superinfection. Neutrophils were the predominant cellular inflammatory infiltrate in the lungs of superinfected mice compared to singly infected animals. Among other cytokines and chemokines, the neutrophil activator granulocyte colony-stimulating factor (G-CSF) was found to be significantly overexpressed in the spleens, lungs, and brains of superinfected animals. High G-CSF protein levels were observed in sera and lung lavage fluid from superinfected animals, suggesting that G-CSF is a major contributor to synergistic exacerbation of disease leading to fatal septicemia.
    Keywords Influenza A virus ; Streptococcus pneumoniae ; animal models ; bacteria ; chemokines ; granulocyte colony-stimulating factor ; lungs ; mice ; neutrophils ; septicemia ; serotypes ; viruses
    Language English
    Size p. 3102-3111.
    Publishing place American Society for Microbiology
    Document type Article
    ZDB-ID 218698-6
    ISSN 1098-5522 ; 0019-9567
    ISSN (online) 1098-5522
    ISSN 0019-9567
    Database NAL-Catalogue (AGRICOLA)

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