ABSTRACT:
The activity of five novel gyrase inhibitors was evaluated against 303 nonduplicate
Pseudomonas aeruginosa
strains collected from 53 North American institutions. The most active compound, GP-2, displayed MIC
50
and MIC
90
values of 1 and 2 μg/ml, respectively. Cross-resistance to other commercially available antipseudomonal compounds was not evident, as no major change was observed in the gyrase inhibitor MIC distribution when stratified by nonsusceptible phenotypes, including the fluoroquinolones and those isolates classified as multidrug resistant (MDR).