Penicillin pharmacodynamics in four experimental pneumococcal infection models

Clinical and animal studies indicate that with optimal dosing, penicillin may still be effective against penicillin-nonsusceptible pneumococci (PNSP). The present study examined whether the same strains of penicillin-susceptible pneumococci (PSP) and PNSP differed in their pharmacodynamic responses to penicillin by using comparable penicillin dosing regimens in four animal models: peritonitis, pneumonia, and thigh infection in mice and tissue cage infection in rabbits. Two multidrug-resistant isolates of Streptococcus pneumoniae type 6B were used, one for which the penicillin MIC was 0.016 mug/ml and the other for which the penicillin MIC was 1.0 mug/ml. Two additional strains of PNSP were studied in the rabbit. The animals were treated with five different penicillin regimens resulting in different maximum concentrations of drugs in serum (C(max)s) and times that the concentrations were greater than the MIC (T(>MIC)s). The endpoints were bacterial viability counts after 6 h of treatment in the mice and 24 h of treatment in the rabbits. Similar pharmacodynamic effects were observed in all models. In the mouse models bactericidal activity depended on the T->MIC and to a lesser extent on the C-max/MIC and the generation time but not on the area under the concentration-time curve (AUC)/MIC. Maximal bactericidal activities were similar for both PSP and PNSP, being the highest in the peritoneum and blood (similar to6 log(10) CFU/ml), followed by the thigh (similar to3 log(10) CFU/thigh), and being the lowest in the lung (similar to1 log(10) CFU/lung). In the rabbit model the maximal effect was similar to6 log(10) CFU/ml after 24 h. In the mouse models bactericidal activity became marked when T->MIC was greater than or equal to 65% of the experimental time and C-max was greater than or equal to 15 times the MIG, and in the rabbit model bactericidal activity became marked when T->MIC was greater than or equal to 35%, C-max was greater than or equal to5 times the MIG, and the AUC at 24 h/MIC exceeded 25. By optimization of the C-max/MIC ratio and T->MIC, the MIC of penicillin for pneumococci can be used to guide therapy and maximize therapeutic efficacy in nonmeningeal infections caused by PNSP.