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Antimicrobial Agents and Chemotherapy, June 2008, p. 2163-2168, Vol. 52, No. 6
0066-4804/08/$08.00+0     doi:10.1128/AAC.01532-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Potency of SMP-601, a Novel Carbapenem, in Hematogenous Murine Bronchopneumonia Caused by Methicillin-Resistant and Vancomycin-Intermediate Staphylococcus aureus{triangledown}

Rie Kihara,1 Katsunori Yanagihara,2,3* Yoshitomo Morinaga,2,3 Nobuko Araki,2 Shigeki Nakamura,3 Masafumi Seki,3 Koichi Izumikawa,3 Hiroshi Kakeya,3 Yoshihiro Yamamoto,3 Kazuhiro Tsukamoto,1 Shimeru Kamihira,2 and Shigeru Kohno3

Department of Pharmacotherapeutics, Nagasaki University Graduate School of Pharmaceutical Sciences,1 Department of Laboratory Medicine,2 Second Department of Internal Medicine, Nagasaki University Graduate School of Medical Sciences, Nagasaki, Japan3

Received 28 November 2007/ Returned for modification 23 January 2008/ Accepted 28 March 2008

We compared the potency of SMP-601, a novel carbapenem, with that of vancomycin in a murine model of hematogenous bronchopneumonia infection caused by methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-intermediate S. aureus (VISA). The MICs of SMP-601 and vancomycin against MRSA were 2 and 1 µg/ml, respectively, while those against VISA were 2 and 8 µg/ml, respectively. Treatment with SMP-601 resulted in a significant decrease in the number of viable bacteria in the MRSA infection model (control, 100 mg/kg vancomycin, and 100 mg/kg SMP-601, 8.42 ± 0.50, 5.29 ± 0.71, and 5.50 ± 0.58 log CFU/lung, respectively,) and in the VISA infection model (control, 100 mg/kg vancomycin, and 100 mg/kg SMP-601, 9.64 ± 0.63, 8.72 ± 0.45, 7.42 ± 0.14 log CFU/lung) (mean ± standard error of the mean). The survival rate in the VISA infection model treated with SMP-601 (70%) was significantly higher than those in the other two groups (20% for vancomycin and 0% for control; P < 0.05). Histopathological examination revealed that inflammatory changes in the SMP-601-treated group were less marked than in the other two groups. The results of pharmacokinetic-pharmacodynamic analysis supported the results of the bacteriological, histopathological and survival studies. Our results demonstrate the potency of SMP-601 against MRSA and VISA in murine hematogenous pulmonary infection.


* Corresponding author. Mailing address: Department of Laboratory Medicine, Nagasaki University School of Medicine, 1-7-1 Sakamoto, Nagasaki 852-8501, Japan. Phone: 81-95-849-7276. Fax: 81-95-849-7285. E-mail: kyana-ngs{at}umin.ac.jp

{triangledown} Published ahead of print on 7 April 2008.


Antimicrobial Agents and Chemotherapy, June 2008, p. 2163-2168, Vol. 52, No. 6
0066-4804/08/$08.00+0     doi:10.1128/AAC.01532-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.







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