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2008-2009 年收集的欧洲和中东地区复杂性皮肤和皮肤组织感染分离株的体外 ceftaroline 及对照抗菌药物活性研究。

In vitro activity of ceftaroline and comparator antimicrobials against European and Middle East isolates from complicated skin and skin-structure infections collected in 2008-2009.

机构信息

Quotient Bioresearch Ltd., Fordham, UK.

出版信息

Int J Antimicrob Agents. 2012 Sep;40(3):227-34. doi: 10.1016/j.ijantimicag.2012.05.014. Epub 2012 Jul 15.

Abstract

The activities of ceftaroline, the active metabolite of the pro-drug ceftaroline fosamil, a novel anti-meticillin-resistant staphylococcal cephalosporin, and nine comparators were determined against surveillance isolates collected in 2008-2009. Over 3000 isolates associated with complicated skin and skin-structure infections (cSSSIs) were collected from 106 centres in 19 countries. MICs were determined using CLSI broth microdilution methodology. Clonal relatedness of meticillin-resistant Staphylococcus aureus (MRSA) with raised ceftaroline MICs (2 mg/L) was assessed by MLST, PFGE and mec typing. The presence of Panton-Valentine leukocidin in these isolates was also determined. Ceftaroline was active against 500 MRSA and 479 meticillin-susceptible S. aureus, with MIC(50/90) values of 0.5/2 mg/L and 0.25/0.25 mg/L, respectively. For coagulase-negative staphylococci (CoNS), the ceftaroline MIC(50/90) values for meticillin-resistant strains (n=159) were the same as those seen for MRSA. Meticillin-susceptible CoNS (n=113) had the same MIC(90) as that seen with S. aureus, but the MIC(50) was lower at 0.06 mg/L. Ceftaroline was also active against β-haemolytic streptococci (n=526; MIC(50/90)=0.004/0.015 mg/L), other streptococci (n=75; 0.015/0.06 mg/L), common Enterobacteriaceae (n=897; 0.25/≥128 mg/L) and Enterococcus faecalis (n=329; 1/16 mg/L). Those MRSA with ceftaroline MICs of 2mg/L were found to be from four clonal groups associated with the country of origin. These data confirm the broad-spectrum in vitro activity of ceftaroline against cSSSI pathogens. Ceftaroline is unique among clinically available cephalosporins, having good in vitro activity against MRSA and meticillin-resistant CoNS and moderate activity against Gram-negative bacteria.

摘要

测定了前药头孢洛林酯的活性代谢物头孢洛林以及新型抗耐甲氧西林葡萄球菌头孢菌素的活性,以及 9 种对照药物对 2008-2009 年收集的监测分离株的活性。从 19 个国家的 106 个中心收集了超过 3000 株与复杂皮肤和皮肤结构感染(cSSSIs)相关的分离株。使用 CLSI 肉汤微量稀释法测定 MIC。通过 MLST、PFGE 和 mec 分型评估了头孢洛林 MIC(2mg/L)升高的耐甲氧西林金黄色葡萄球菌(MRSA)的克隆相关性。还确定了这些分离株中是否存在杀白细胞素。头孢洛林对 500 株 MRSA 和 479 株耐甲氧西林金黄色葡萄球菌具有活性,MIC(50/90)值分别为 0.5/2mg/L 和 0.25/0.25mg/L。对于凝固酶阴性葡萄球菌(CoNS),头孢洛林对耐甲氧西林菌株(n=159)的 MIC(50/90)值与 MRSA 相同。耐甲氧西林凝固酶阴性葡萄球菌(n=113)的 MIC(90)与金黄色葡萄球菌相同,但 MIC(50)较低,为 0.06mg/L。头孢洛林对β-溶血性链球菌(n=526;MIC(50/90)=0.004/0.015mg/L)、其他链球菌(n=75;0.015/0.06mg/L)、常见肠杆菌科(n=897;0.25/≥128mg/L)和粪肠球菌(n=329;1/16mg/L)也具有活性。头孢洛林 MIC 为 2mg/L 的这些 MRSA 来自与起源国相关的四个克隆群。这些数据证实了头孢洛林对 cSSSI 病原体具有广泛的体外活性。头孢洛林在临床上可用的头孢菌素中是独一无二的,对 MRSA 和耐甲氧西林凝固酶阴性葡萄球菌具有良好的体外活性,对革兰氏阴性菌具有中度活性。

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