Affiliation:
1. Division of Infectious Diseases, Department of Medicine, The Children's Hospital Medical Center, and Department of Pediatrics, Harvard Medical School, Boston, Massachusetts 02115
Abstract
To evaluate ampicillin (Amp) and chloramphenicol (Cm) alone and in combination againstHaemophilus influenzaetype b, we examined the viability of 5 log10colony-forming units (CFU) of early-log-phase organisms per ml after 4 and 8 h of incubation with the drug(s). Nine Amp-susceptible (Amps) and five Amp-resistant (Ampr) systemic isolates were examined. Antibiotic concentrations included: the minimum inhibitory concentration (MIC) of Amp, 50% of the MIC of Amp, 25% of the MIC of Amp, the MIC of Cm, 50% of the MIC of Cm, 25% of the MIC of Cm, and nine combinations of these concentrations. Both Amp and Cm at their MIC significantly reduced bacterial titers of AmpsH. influenzaetype b after 8 h of incubation (1.36 and 1.47 log10CFU/ml, respectively; bothp< 0.01); only Cm at its MIC significantly reduced the number of viable organisms after 4 h (0.91 log10CFU/ml;P< 0.001). With Amprorganisms, significant reductions in mean bacterial titers occurred after 4 and 8 h of incubation in the presence of Amp at its MIC (1.66 and 2.06 log10CFU/ml, respectively; bothP< 0.02); smaller but significant reductions were noted after 4 and 8 with Cm at its MIC (0.56 and 0.87 log20CFU/ml, respectively; bothP< 0.025). Antagonism with Ampsor Amprstrains was not seen. We conclude that combinations of Amp and Cm have indifferent effects on Ampsand AmprH. influenzaetype b.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
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