The in vitro susceptibilities of 150 clinical isolates of Pseudomonas aeruginosa to the aminoglycoside tobramycin and eight other antimicrobials were evaluated. The Food and Drug Administration standardized disk diffusion method showed that tobramycin inhibited 100% of the 150 isolates with gentamicin inhibiting only 90.7%. The difference between colistin (97.3%) and tobramycin was less marked. Carbenicillin (87.3%) was found to be slightly less active than gentamicin. Only a small percentage of the isolates were inhibited by the other drugs used. By using a minimal inhibitory concentration of 4 ,ug/ml in brain heart infusion broth as the level of susceptibility, it was found that only three of the isolates showed resistance to tobramycin, whereas 20 of the isolates were resistant to gentamicin. Approximately half of the isolates were inhibited by 0.5 Mg/ml or less of tobramycin, whereas 1.5 Mg of gentamicin per ml was required to inhibit 50% of susceptible strains.Tobramycin (17) has been evaluated by both the disk diffusion method and the broth dilution method with regard to its in vitro activity against a variety of gram-negative bacilli. Included in many studies are isolates of Pseudomonas aeruginosa (3-5, 7, 8, 12, 13, 15, 16, 19). This study was undertaken to evaluate a sample of consecutive clinical isolates of P. aeruginosa for their susceptibility to tobramycin, gentamicin, colistin, carbenicillin, ampicillin, kanamycin, cephalothin, chloramphenicol, and tetracycline hydrochloride. Due to conflicting reports concerning the comparable efficacy of tobramycin and gentamicin (3,5,7,15,16), both the disk method and broth dilution method were used for these two drugs with only the disk diffusion method being used for the other seven drugs.
MATERIALS AND METHODSIsolates. Through the cooperation of the Director of Clinical Laboratories of the University Hospital, University of Mississippi Medical Center, consecutive isolates of Pseudomonas from clinical specimens were obtained. Each isolate was plated on eosin methylene blue agar (Difco) to assure purity, and a mixed colonial population was transferred to triple sugar iron (TSI) agar (Difco) slants for initial confirmation of identification. The isolates were then inoculated to pigment production medium A and B of King et al. (11). A total of 150 isolates producing pyocyanin on the A medium (10) with colonial morphology and reactions on TSI typical of P. aeruginosa were used in subsequent antibiotic testing. After confirmation of identification, the isolates were transferred to brain heart infusion agar (Difco) slants, incubated overnight at 37 C, and stored at 4 C until tested. The storage time of an isolate usually was less than 2 weeks and never exceeded 6 weeks.