Kosowska-Shick Klaudia, Ednie Lois M, McGhee Pamela, Appelbaum Peter C
Hershey Medical Center, Hershey, PA 17033, USA.
Antimicrob Agents Chemother. 2009 Jun;53(6):2239-47. doi: 10.1128/AAC.01531-08. Epub 2009 Mar 23.
For 297 penicillin-susceptible, -intermediate, and -resistant pneumococcal strains, the sulopenem MIC(50)s were 0.008, 0.06, and 0.25, respectively, and the sulopenem MIC(90)s were 0.016, 0.25, and 0.5 microg/ml, respectively. The MIC(50)s of amoxicillin for the corresponding strains were 0.03, 0.25, and 2.0 microg/ml, respectively, and the MIC(90)s were 0.03, 1.0, and 8.0 microg/ml, respectively. The combination of amoxicillin and clavulanate gave MICs similar to those obtained with amoxicillin alone. The sulopenem MICs were similar to those of imipenem and meropenem. The MICs of ss-lactams increased with those of penicillin G, and among the quinolones tested, moxifloxacin had the lowest MICs. Additionally, 45 strains of drug-resistant type 19A pneumococci were tested by agar dilution and gave sulopenem MIC(50)s and MIC(90)s of 1.0 and 2.0 microg/ml, respectively. Both sulopenem and amoxicillin (with and without clavulanate) were bactericidal against all 12 strains tested at 2x MIC after 24 h. Thirty-one strains from 10 countries with various penicillin, amoxicillin, and carbapenems MICs, including those with the highest sulopenem MICs, were selected for sequencing analysis of the pbp1a, pbp2x, and pbp2b regions encoding the transpeptidase active site and MurM. We did not find any correlations between specific penicillin-binding protein-MurM patterns and changes in the MICs.
对于297株对青霉素敏感、中介和耐药的肺炎球菌菌株,舒洛培南的MIC50分别为0.008、0.06和0.25,舒洛培南的MIC90分别为0.016、0.25和0.5μg/ml。相应菌株的阿莫西林MIC50分别为0.03、0.25和2.0μg/ml,MIC90分别为0.03、1.0和8.0μg/ml。阿莫西林与克拉维酸联合使用时的MIC与单独使用阿莫西林时相似。舒洛培南的MIC与亚胺培南和美罗培南相似。β-内酰胺类药物的MIC随青霉素G的MIC升高而升高,在所测试的喹诺酮类药物中,莫西沙星的MIC最低。此外,通过琼脂稀释法对45株耐药的19A血清型肺炎球菌进行了测试,舒洛培南的MIC50和MIC90分别为1.0和2.0μg/ml。舒洛培南和阿莫西林(含或不含克拉维酸)在2倍MIC浓度下对所有12株测试菌株作用24小时后均具有杀菌作用。从10个国家选取了31株具有不同青霉素、阿莫西林和碳青霉烯类药物MIC的菌株,包括舒洛培南MIC最高的菌株,对编码转肽酶活性位点和MurM的pbp1a、pbp2x和pbp2b区域进行测序分析。我们未发现特定青霉素结合蛋白-MurM模式与MIC变化之间存在任何相关性。