We tested the antimicrobial activities of meropenem (MEPM), imipenem (IPM), panipenem (PAPM), piperacillin (PIPC), cefepime (CFPM), aztreonam (AZT), amikacin (AMK), and levofloxacin (LVFX) against 106 clinical
Pseudomonas aeruginosa isolates and 64 clinical
Acinetobacter spp. iso lates with reduced susceptibility to carbapenems. Using NCCLS breakpoints, the percentages of
P. aeruginosa strains susceptible to AMK and
Acinetobacter spp. strains susceptible to LVFX were found to be 51.1% and 55.6%, respectively, which represented the highest activity among 8 antimicrobial agents in each organism. Referring to the correlations among MICs of carbapenems, MEPM showed a higher activity than IPM and PAPM in both organisms; 29 of the 94 strains (30.9%) of IPMresistant P. aeruginosa were susceptible to MEPM. Further study for resistance mechanisms to carbapenems by the disk diffusion method using 2-mercaptopropionic acid revealed that 8 of the 64
Acinetobacter spp. isolates (12.5%) were metallo-β-lactamase producers, while none of 106 P. aeruginosa isolates were metallo-β-lactamase producers. PCR analysis using blaIMP-specific primers confirmed that 4 of the 8 metallo-β-lactamase-producing
Acinetobacter spp. isolates detected by the disk diffusion method were carrying the
blaIMP gene. The identification of metallo-β-lactamase-producing
Acinetobacter spp. isolates implies that metallo-β-lactamase genes have been disseminated among various gramnegative pathogens.
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