morphological and bactericidal effects of amikacin, meropenem and imipenem on pseudomonas aeruginosa

conclusions induction of coccoid form of p. aeruginosa may be one of the important reasons for antibiotic treatment failure; therefore, prescribed dose of antibiotics should be carefully managed to prevent increasing antibiotic resistance and coccoid bacteria induction. results all used antibiotics at sub mic concentration had capability to induce coccoid bacteria. the highest rate of induced coccoid bacteria was 98.2% after 8 days, with contribution of imipenem and meropenem at 2 μg/ml concentration. amikacin at 4 μg/ml concentration induced lower rate of coccoid bacteria (55.05%). amikacin had a strong bactericidal effect on coccoid bacteria at 8 μg/ml concentration. imipenem and meropenem showed very weak bactericidal effect on coccoid bacteria. materials and methods eight p. aeruginosa isolates obtained from clinical samples of burned patients and standard strain atcc 27853 were used in this study. isolates were identified by biochemical tests and confirmed by pcr method using its specific primer. minimum inhibitory concentrations (mics) of three antibiotics were determined by e-test method. bacteria were exposed to antibiotics at different concentrations. bacterial morphology in different days was examined by specific microscope and viability of isolates was examined by flow cytometry objectives the aim of this study was to determine in vitro morphological and bactericidal effects of amikacin, meropenem and imipenem on p. aeruginosa isolated from clinical specimens. background pseudomonas aeruginosa might be converted to coccoid bacteria under antibiotic stress. bacterial conversion would increase resistance to antibiotics due to changes in cell wall crosslink or decreased metabolic activity. morphology of p. aeruginosa under stress conditions (presence of antibiotics) can be changed to elongated bacilli, u shape and finally coccoid bacteria. results of several researches showed that coccoid bacteria are one of the most important aspects of drug resistance. it would be the major reason for treatment failure.