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Infection and Immunity, December 2006, p. 6707-6721, Vol. 74, No. 12
0019-9567/06/$08.00+0     doi:10.1128/IAI.00789-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

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

Lynnelle A. McNamee* and Allen G. Harmsen

Veterinary Molecular Biology Department, Montana State University, Molecular Biosciences Bldg., 960 Technology Blvd., Bozeman, Montana 59718

Received 16 May 2006/ Returned for modification 5 July 2006/ Accepted 6 September 2006

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.

* Corresponding author. Mailing address: Veterinary Molecular Biology Department, 960 Technology Blvd., Bozeman, MT 59718. Phone: (406) 994-7697. Fax: (406) 994-4303. E-mail: mcnamela{at}yahoo.com.

{triangledown} Published ahead of print on 18 September 2006.

Editor: R. P. Morrison

Infection and Immunity, December 2006, p. 6707-6721, Vol. 74, No. 12
0019-9567/06/$08.00+0     doi:10.1128/IAI.00789-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.



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