Service de Bactériologie-Virologie-Hygiène, CHU Henri Mondor, Assistance Publique-Hôpitaux de Paris, Université Paris 12, 94010 Créteil Cedex, France.
Int J Antimicrob Agents. 2011 Mar;37(3):235-9. doi: 10.1016/j.ijantimicag.2010.11.035. Epub 2011 Feb 4.
The aims of this study were to determine the in vitro activity profile of ceftobiprole, a pyrrolidinone cephalosporin, against a large number of bacterial pathogens and to propose zone diameter breakpoints for clinical categorisation according to the European Committee on Antimicrobial Susceptibility Testing (EUCAST) minimum inhibitory concentration (MIC) breakpoints. MICs of ceftobiprole were determined by broth microdilution against 1548 clinical isolates collected in eight French hospitals. Disk diffusion testing was performed using 30 μg disks according to the method of the Comité de l'Antibiogramme de la Société Française de Microbiologie (CA-SFM). The in vitro activity of ceftobiprole, expressed by MIC(50/90) (MICs for 50% and 90% of the organisms, respectively) (mg/L), was as follows: meticillin-susceptible Staphylococcus aureus, 0.25/0.5; meticillin-resistant S. aureus (MRSA), 1/2; meticillin-susceptible coagulase-negative staphylococci (CoNS), 0.12/0.5; meticillin-resistant CoNS, 1/2; penicillin-susceptible Streptococcus pneumoniae, ≤ 0.008/0.03; penicillin-resistant S. pneumoniae, 0.12/0.5; viridans group streptococci, 0.03/0.12; β-haemolytic streptococci, ≤ 0.008/0.016; Enterococcus faecalis, 0.25/1; Enterococcus faecium, 64/128; Enterobacteriaceae, 0.06/32; Pseudomonas aeruginosa, 4/16; Acinetobacter baumannii, 0.5/64; Haemophilus influenzae, 0.03/0.12; and Moraxella catarrhalis, 0.25/0.5. According to the regression curve, zone diameter breakpoints could be 28, 26, 24 and 22 mm for MICs of 0.5, 1, 2 and 4 mg/L respectively. In conclusion, this study confirms the potent in vitro activity of ceftobiprole against many Gram-positive bacteria, including MRSA but not E. faecium, whilst maintaining a Gram-negative spectrum similar to the advanced-generation cephalosporins such as cefepime. Thus ceftobiprole appears to be well suited for the empirical treatment of a variety of healthcare-associated infections.
本研究旨在确定头孢托罗匹酯(一种吡咯烷酮头孢菌素)对大量细菌病原体的体外活性,并根据欧洲抗菌药物敏感性试验委员会(EUCAST)最低抑菌浓度(MIC)折点提出用于临床分类的抑菌圈直径折点。采用肉汤微量稀释法对来自法国 8 家医院的 1548 株临床分离株进行了头孢托罗匹酯 MIC 测定。采用 30μg 药敏纸片,按法国微生物学会药敏试验委员会(CA-SFM)方法进行药敏纸片扩散试验。头孢托罗匹酯的体外活性以 MIC(50/90)(分别为 50%和 90%受试菌的 MIC)表示,结果如下:甲氧西林敏感金黄色葡萄球菌为 0.25/0.5;耐甲氧西林金黄色葡萄球菌(MRSA)为 1/2;甲氧西林敏感凝固酶阴性葡萄球菌(CoNS)为 0.12/0.5;耐甲氧西林凝固酶阴性葡萄球菌(MRCoNS)为 1/2;青霉素敏感肺炎链球菌≤0.008/0.03;青霉素耐药肺炎链球菌为 0.12/0.5;草绿色链球菌属为 0.03/0.12;β-溶血性链球菌属≤0.008/0.016;粪肠球菌为 0.25/1;屎肠球菌为 64/128;肠杆菌科细菌为 0.06/32;铜绿假单胞菌为 0.04/0.16;鲍曼不动杆菌为 0.5/64;流感嗜血杆菌为 0.03/0.12;卡他莫拉菌为 0.25/0.5。根据回归曲线,对于 MIC 为 0.5、1、2 和 4mg/L 的头孢托罗匹酯,抑菌圈直径折点分别为 28、26、24 和 22mm。总之,本研究证实头孢托罗匹酯对许多革兰阳性菌具有较强的体外活性,包括耐甲氧西林金黄色葡萄球菌(但不包括屎肠球菌),同时保持与头孢吡肟等第三代头孢菌素相似的革兰阴性谱。因此,头孢托罗匹酯似乎非常适合用于治疗各种与医疗保健相关的感染。