Synergistic stimulation of type I interferons during influenza virus coinfection promotes Streptococcus pneumoniae colonization in mice.

Abstract

Pneumococcal infection of the respiratory tract is often secondary to recent influenza virus infection and accounts for much of the morbidity and mortality during seasonal and pandemic influenza. Here, we show that coinfection of the upper respiratory tract of mice with influenza virus and pneumococcus leads to synergistic stimulation of type I IFNs and that this impairs the recruitment of macrophages, which are required for pneumococcal clearance, due to decreased production of the chemokine CCL2. Type I IFN expression was induced by pneumococcal colonization alone. Colonization followed by influenza coinfection led to a synergistic type I IFN response, resulting in increased density of colonizing bacteria and susceptibility to invasive infection. This enhanced type I IFN response inhibited production of the chemokine CCL2, which promotes the recruitment of macrophages and bacterial clearance. Stimulation of CCL2 by macrophages upon pneumococcal infection alone required the pattern recognition receptor Nod2 and expression of the pore-forming toxin pneumolysin. Indeed, the increased colonization associated with concurrent influenza virus infection was not observed in mice lacking Nod2 or the type I IFN receptor, or in mice challenged with pneumococci lacking pneumolysin. We therefore propose that the synergistic stimulation of type I IFN production during concurrent influenza virus and pneumococcal infection leads to increased bacterial colonization and suggest that this may contribute to the higher rates of disease associated with coinfection in humans.

• Authors: Shigeki Nakamura, Kimberly M Davis, Jeffrey N Weiser
• Journal: The Journal of clinical investigation (J Clin Invest) Vol. 121 Issue 9 Pg. 3657-65 (Sep 2011) ISSN: 1558-8238 [Electronic] United States
• PMID: 21841308 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)

Chemical References

• Chemokine CCL2
• Interferon Type I
• Nod2 Signaling Adaptor Protein
• Nod2 protein, mouse

Topics

• Animals
• Cells, Cultured
• Chemokine CCL2 (immunology)
• Female
• Interferon Type I (immunology)
• Macrophages (cytology, immunology)
• Male
• Mice
• Mice, Inbred C57BL
• Mice, Knockout
• Nod2 Signaling Adaptor Protein (genetics, metabolism)
• Orthomyxoviridae (immunology, pathogenicity)
• Orthomyxoviridae Infections (complications, immunology, microbiology, virology)
• Pneumococcal Infections (etiology, immunology, microbiology, virology)
• Streptococcus pneumoniae (immunology, pathogenicity)
• Trachea (immunology, microbiology, virology)