Impairment of Antibacterial Defense Mechanisms of the Lung by Extrapulmonary Infection

• Published in: The Journal of infectious diseases 1986-02, Vol.153 (2), p.202-208
• Main Authors: White, Jon C., Nelson, Steve, Winkelstein, Jerry A., Booth, Frank V. McL, Jakab, George J.
• Format: Article
• Language: English
• Subjects: Aerosols; Animals; Antibacterials; Bacteria; Bacterial diseases; Biological and medical sciences; Caseins - pharmacology; Complement C3 - analysis; Complement C5 - analysis; Escherichia coli; Escherichia coli Infections - complications; Escherichia coli Infections - immunology; Experimental bacterial diseases and models; Female; Glycogen - pharmacology; Infections; Infectious diseases; Inhalation; Lung - immunology; Lung - microbiology; Lung Diseases - complications; Lung Diseases - immunology; Lungs; Macrophages, Peritoneal - immunology; Medical sciences; Mice; Mortality; Neutrophils - immunology; Original Articles; Peritoneal Cavity - microbiology; Peritonitis; Peritonitis - complications; Peritonitis - immunology; Pseudomonas aeruginosa; Pseudomonas Infections - complications; Pseudomonas Infections - immunology; Sepsis; Staphylococcal Infections - complications; Staphylococcal Infections - immunology
• ISSN: 0022-1899; 1537-6613
• DOI: 10.1093/infdis/153.2.202

To determine whether extrapulmonary infection alters antibacterial defenses of the lung, we challenged mice with peritonitis due to Escherichia coli by aerosol inhalation with either Staphylococus aureus or Pseudomonas aeruginosa. In animals without peritonitis, 14070 ± 5070 and 11 070 ± 1070 of the initially deposited viable S. aureus and P. aeruginosa, respectively, remained in the lungs at 4 hr. In contrast, in mice with peritonitis, at 4 hr 45% ± 9% of the staphylococci were recoved, and the P. aeruginosa had increased to 948% ± 354% of the initial inoculum. Proliferation of P. aeruginosa in mice with peritonitis was associated with impaired recruitment of polymorphonuclear neutrophils (PMNs) into the lungs. In contrast, a noninfectious stimulus induced more PMNs into the peritoneal cavity than did intraabdominal sepsis but only minimally impaired PMN recruitment into the lungs after aerosol challenge with P. aeruginosa. Sterile intraperitoneal stimulation did not significantly impair intrapulmonary killing of P. aeruginosa. Levels of antigenic C3 and functionally active C5 were significantly depleted in mice with peritonitis due to E. coli. We conclude that the systemic effects of sepsis, including complement depletion, contribute to the decreased pulmonary PMN recruitment and to impaired intrapulmonary bacterial killing of animals with peritonitis due to E. coli.