8-hydroxy-11-12-epoxyeicosa-5-9-14-trienoic-acid and Pneumococcal-Infections

Topics: 8,11,14-Eicosatrienoic Acid; Animals; Arachidonate 12-Lipoxygenase; Bacillus subtilis; Bacterial Proteins; Bacterial Toxins; Cell Line; Cell Membrane; Clostridium septicum; Female; Humans; Mice; Mice, Inbred C57BL; Mice, Knockout; Neutrophil Infiltration; Neutrophils; Pneumococcal Infections; Streptococcus pneumoniae; Streptolysins; Transendothelial and Transepithelial Migration; Virulence Factors

Acute pulmonary infection by Streptococcus pneumoniae is characterized by high bacterial numbers in the lung, a robust alveolar influx of polymorphonuclear cells (PMNs), and a risk of systemic spread of the bacterium. We investigated host mediators of S. pneumoniae-induced PMN migration and the role of inflammation in septicemia following pneumococcal lung infection. Hepoxilin A3 (HXA3) is a PMN chemoattractant and a metabolite of the 12-lipoxygenase (12-LOX) pathway. We observed that S. pneumoniae infection induced the production of 12-LOX in cultured pulmonary epithelium and in the lungs of infected mice. Inhibition of the 12-LOX pathway prevented pathogen-induced PMN transepithelial migration in vitro and dramatically reduced lung inflammation upon high-dose pulmonary challenge with S. pneumoniae in vivo, thus implicating HXA3 in pneumococcus-induced pulmonary inflammation. PMN basolateral-to-apical transmigration in vitro significantly increased apical-to-basolateral transepithelial migration of bacteria. Mice suppressed in the expression of 12-LOX exhibited little or no bacteremia and survived an otherwise lethal pulmonary challenge. Our data suggest that pneumococcal pulmonary inflammation is required for high-level bacteremia and systemic infection, partly by disrupting lung epithelium through 12-LOX-dependent HXA3 production and subsequent PMN transepithelial migration.

Topics: 8,11,14-Eicosatrienoic Acid; Animals; Arachidonate 12-Lipoxygenase; Bacillus subtilis; Bacteremia; Cell Line, Tumor; Cell Movement; Chemotactic Factors; Humans; Inflammation; Lung; Lung Diseases; Mice; Mice, Inbred C57BL; Mice, Knockout; Neutrophils; Pneumococcal Infections; Streptococcus pneumoniae; Transendothelial and Transepithelial Migration