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Bacterial Infections

Both Influenza-Induced Neutrophil Dysfunction and Neutrophil-Independent Mechanisms Contribute to Increased Susceptibility to a Secondary Streptococcus pneumoniae Infection

Lynnelle A. McNamee, Allen G. Harmsen
Lynnelle A. McNamee
Veterinary Molecular Biology Department, Montana State University, Molecular Biosciences Bldg., 960 Technology Blvd., Bozeman, Montana 59718
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  • For correspondence: mcnamela@yahoo.com
Allen G. Harmsen
Veterinary Molecular Biology Department, Montana State University, Molecular Biosciences Bldg., 960 Technology Blvd., Bozeman, Montana 59718
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DOI: 10.1128/IAI.00789-06
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ABSTRACT

Since secondary Streptococcus pneumoniae infections greatly increase the mortality of influenza infections, we determined the relative roles of neutrophil-dependent and -independent mechanisms in increased susceptibility to S. pneumoniae during influenza infection. Mice infected with influenza for 6 days, but not 3 days, showed a significant increase in susceptibility to S. pneumoniae infection compared to mice not infected with influenza. There was significant neutrophil accumulation in the lungs of S. pneumoniae-infected mice regardless of whether or not they were infected with influenza for 3 or 6 days. Depletion of neutrophils in these mice resulted in increased susceptibility to S. pneumoniae in both the non-influenza-infected mice and mice infected with influenza for 3 days but not in the mice infected with influenza for 6 days, indicating that a prior influenza infection of 6 days may compromise neutrophil function, resulting in increased susceptibility to a S. pneumoniae infection. Neutrophils from the lungs of mice infected with influenza for 3 or 6 days exhibited functional impairment in the form of decreased phagocytosis and intracellular reactive oxygen species generation in response to S. pneumoniae. In addition, neutrophil-depleted mice infected with influenza for 6 days were more susceptible to S. pneumoniae than neutrophil-depleted mice not infected with influenza, indicating that neutrophil-independent mechanisms also contribute to influenza-induced increased susceptibility to S. pneumoniae. Pulmonary interleukin-10 levels were increased in coinfected mice infected with influenza for 6 days but not 3 days. Thus, an influenza infection of 6 days increases susceptibility to S. pneumoniae by both suppression of neutrophil function and by neutrophil-independent mechanisms such as enhanced cytokine production.

  • Copyright © 2006 American Society for Microbiology
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Both Influenza-Induced Neutrophil Dysfunction and Neutrophil-Independent Mechanisms Contribute to Increased Susceptibility to a Secondary Streptococcus pneumoniae Infection
Lynnelle A. McNamee, Allen G. Harmsen
Infection and Immunity Nov 2006, 74 (12) 6707-6721; DOI: 10.1128/IAI.00789-06

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Both Influenza-Induced Neutrophil Dysfunction and Neutrophil-Independent Mechanisms Contribute to Increased Susceptibility to a Secondary Streptococcus pneumoniae Infection
Lynnelle A. McNamee, Allen G. Harmsen
Infection and Immunity Nov 2006, 74 (12) 6707-6721; DOI: 10.1128/IAI.00789-06
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KEYWORDS

Leukocyte Disorders
neutrophils
Orthomyxoviridae Infections
Pneumonia, Pneumococcal

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