Implanted
medical devices such as central venous catheters are
highly susceptible to microbial colonization and biofilm formation
and are a major risk factor for nosocomial infections. The opportunistic
pathogen Pseudomonas aeruginosa uses
exopolysaccharides, such as Psl, for both initial surface attachment
and biofilm formation. We have previously shown that chemically immobilizing
the Psl-specific glycoside hydrolase, PslGh, to a material
surface can inhibit P. aeruginosa biofilm
formation. Herein, we show that PslGh can be uniformly
immobilized on the lumen surface of medical-grade, commercial polyethylene,
polyurethane, and polydimethylsiloxane (silicone) catheter tubing.
We confirmed that the surface-bound PslGh was uniformly
distributed along the catheter length and remained active even after
storage for 30 days at 4 °C. P. aeruginosa colonization and biofilm formation under dynamic flow culture conditions in vitro showed a 3-log reduction in the number of bacteria
during the first 11 days, and a 2-log reduction by day 14 for PslGh-modified PE-100 catheters, compared to untreated catheter
controls. In an in vivo rat infection model, PslGh-modified PE-100 catheters showed a ∼1.5-log reduction
in the colonization of the clinical P. aeruginosa ATCC 27853 strain after 24 h. These results demonstrate the robust
ability of surface-bound glycoside hydrolase enzymes to inhibit biofilm
formation and their potential to reduce rates of device-associated
infections.