Journal of Antimicrobial Chemotherapy (1994) 33, 765-775
© 1994 The British Society for Antimicrobial Chemotherapy
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The effect of erythromycin on Pseudomonas aeruginosa and neutrophil mediated epithelial damage
aHost Defence Unit, National Heart & Lung Institute Emmanuel Kaye Building, Manresa Road, London SW36LR bRoyal Postgraduate Medical School, Hammersmith Hospital Du Cane Road, London W120HS, UK cDepartment of Infection & Inflammation, Chest Disease Research Institute, Kyoto University Kyoto, 606, Japan
Received 20 April 1993; accepted 23 November 1993
*Corresponding author
Erythromycin therapy for long periods may benefit patients with chronic bronchial sepsis colonized by Pseudomonas aeruginosa despite the lack of antibacterial activity. We have investigated the effect of filtrates of 24 h P. aeruginosa cultures (CF) with or without erythromycin 05, 5, 20mg/L on human nasal epithelium in the absence or presence of polymorphonuclear leucocytes (PMN). Ciliary beat frequency (CBF) and epithelium integrity were examined for 4 h. Erythromycin (20 mg/L) alone did not affect epithelium. CF without erythromycin slowed CBF by 635% of control at 4 h, and caused disruption of surface integrity in 80% of the epithelium. Addition of erythromycin to CF did not inhibit these effects. Erythromycin did not affect growth of P. aeruginosa. Filtrates of P. aeruginosa cultured with erythromycin (5 and 20 mg/L) caused less CBF slowing (372% and 192% of control, respectively) and epithelial disruption (42% and 67%, respectively). Unstimulated PMN (107/mL) slowed CBF by 13% of control at 4 h but did not cause epithelial disruption. PMN and CF together slowed CBF (954% of control) and damaged epithelium (933% of epithelium disrupted) synergically. Pre-incubation of PMN with erythromycin did not inhibit these effects. PMN and filtrates of P. aeruginosa cultured with erythromycin (5 and 20 mg/L) caused less CBF slowing (580% and 336% of control, respectively) and epithelial disruption (400% and 133%, respectively). Erythromycin may benefit patients by reducing P. aeruginosa production of factors which damage epithelium and stimulate neutrophil mediated cytotoxicity.
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