INTERACTION OF PSEUDOMONAS-AERUGINOSA WITH HUMAN RESPIRATORY MUCOSA IN-VITRO

Citation
Kwt. Tsang et al., INTERACTION OF PSEUDOMONAS-AERUGINOSA WITH HUMAN RESPIRATORY MUCOSA IN-VITRO, The European respiratory journal, 7(10), 1994, pp. 1746-1753
Citations number
64
Categorie Soggetti
Respiratory System
ISSN journal
09031936
Volume
7
Issue
10
Year of publication
1994
Pages
1746 - 1753
Database
ISI
SICI code
0903-1936(1994)7:10<1746:IOPWHR>2.0.ZU;2-N
Abstract
Pseudomonas aeruginosa commonly infects the airways of patients with c ystic fibrosis and bronchiectasis. It produces several toxins that slo w ciliary beat, stimulate mucus production and damage epithelium. It a dheres to epithelial cells, damaged mucosa (in animal models), and muc us. However, little is known of the interaction of P. aeruginosa with intact human respiratory mucosa We have studied the interactions of a nonmucoid clinical isolate of P. aeruginosa with adenoid tissue in a n ovel organ culture model with an air-mucosal interphase P. aeruginosa (5.9+/-0.9x10(6) colony-forming units (cfu)) was pipetted onto the org an culture surface, and incubated for 15 min, 1, 2, 4, 8, 12, 16, and 24 h, at 37 degrees C in 5% CO2 in a humidified atmosphere. Assessment has been made by transmission and scanning electron microscopy. Trans mission electron microscopy (TEM) showed that uninfected organ culture s had normal ultrastructure. TEM of infected organ cultures at 8 h sho wed significant epithelial damage: 43.9+/-10% of cells extruding from the epithelial surface, 17.7+/-3% of cells with loss of cilia, 32.9+/- 10.22 of cells with mitochondrial damage, and 11.6+/-3% of cells with cytoplasmic blebbing. P. aeruginosa only infrequently adhered to norma l epithelium, but adhered to areas of epithelial damage and to basemen t membrane. Scanning electron microscopy (SEM) of organ cultures up to 2 h found P. aeruginosa only infrequently associated with mucus. SEM at 4 h revealed P. aeruginosa predominantly associated with mucus and extruded damaged epithelial cells, but also occasionally associated wi th cilia, and very occasionally with unciliated cells. SEM also reveal ed loss of epithelial tight junctions in P. aeruginosa infected organ cultures, and P. aeruginosa were frequently seen in the gaps between e pithelial cells. An extracellular matrix, possibly of bacterial origin , was seen bridging the space between bacteria and cell surface. We co nclude that P. aeruginosa infection of this organ culture caused tissu e damage and that P. aeruginosa preferentially adhered to mucus, damag ed epithelium and basement membrane.