JMI Laboratories, North Liberty, IA, USA.
JMI Laboratories, North Liberty, IA, USA.
Diagn Microbiol Infect Dis. 2014 Apr;78(4):422-8. doi: 10.1016/j.diagmicrobio.2013.08.027. Epub 2014 Jan 18.
Ceftaroline, the active metabolite of the prodrug ceftaroline fosamil, is a new cephalosporin with bactericidal activity against resistant Gram-positive organisms including methicillin-resistant Staphylococcus aureus (MRSA) and multidrug-resistant strains of Streptococcus pneumoniae, and commonly isolated Gram-negative organisms, including ceftriaxone-susceptible Enterobacteriaceae. We evaluated the in vitro activity of ceftaroline and selected comparator agents against bacterial isolates collected from patients with acute bacterial skin and skin structure infections (ABSSSIs) in the USA. A total of 6222 isolates were collected from 67 medical centers distributed across all nine USA census regions between 2009 and 2011 and tested for susceptibility by reference broth microdilution methods. Ceftaroline was very active against S. aureus (MIC50/90, 0.5/1 μg/mL; 99.6% susceptible), including MRSA (MIC50/90, 0.5/1 μg/mL; 99.1% susceptible). Against β-hemolytic streptococci, the activity of ceftaroline (MIC50/90, ≤0.015/0.03 μg/mL; 100.0% susceptible) was comparable to that of both penicillin (MIC50/90, ≤0.06/≤0.06 μg/mL; 100.0% susceptible) and ceftriaxone (MIC50/90, ≤0.25/≤0.25 μg/mL; 100.0% susceptible). Ceftaroline was also highly active against viridans group streptococci (MIC50/90, 0.03/0.06 μg/mL). Similar to ceftriaxone and ceftazidime, ceftaroline was active against wild-type strains of Escherichia coli (MIC50/90, 0.12/0.25 μg/mL; 94.0% susceptible) and Klebsiella pneumoniae (MIC50/90, 0.12/0.25 μg/mL; 96.8% susceptible); however, the ceftaroline activity was compromised among strains with an extended-spectrum β-lactamase-phenotype (MIC50/90, >32/>32 μg/mL for both E. coli and K. pneumoniae). In summary, ceftaroline showed potent activity against a large contemporary collection (6222) of bacterial isolates associated with ABSSSI in the USA.
头孢洛林是前体药物头孢洛林酯的活性代谢物,是一种新型头孢菌素,对包括耐甲氧西林金黄色葡萄球菌(MRSA)和多药耐药肺炎链球菌以及常见分离的革兰氏阴性菌在内的耐药革兰氏阳性菌具有杀菌活性。我们评估了头孢洛林及其选定的对照药物对 2009 年至 2011 年间美国采集的急性细菌性皮肤和皮肤结构感染(ABSSSI)患者的细菌分离株的体外活性。共有 6222 株分离株来自美国九个普查区的 67 个医疗中心,通过参考肉汤微量稀释法进行了药敏试验。头孢洛林对金黄色葡萄球菌(MIC50/90,0.5/1μg/mL;99.6%敏感),包括耐甲氧西林金黄色葡萄球菌(MIC50/90,0.5/1μg/mL;99.1%敏感)具有很强的活性。对于β-溶血性链球菌,头孢洛林的活性(MIC50/90,≤0.015/0.03μg/mL;100.0%敏感)与青霉素(MIC50/90,≤0.06/≤0.06μg/mL;100.0%敏感)和头孢曲松(MIC50/90,≤0.25/≤0.25μg/mL;100.0%敏感)相当。头孢洛林对草绿色链球菌也具有很高的活性(MIC50/90,0.03/0.06μg/mL)。与头孢曲松和头孢他啶相似,头孢洛林对大肠埃希菌(MIC50/90,0.12/0.25μg/mL;94.0%敏感)和肺炎克雷伯菌(MIC50/90,0.12/0.25μg/mL;96.8%敏感)的野生型菌株均具有活性;然而,在具有扩展谱β-内酰胺酶表型的菌株中,头孢洛林的活性受到了损害(MIC50/90,大肠埃希菌和肺炎克雷伯菌均>32/32μg/mL)。总之,头孢洛林对美国 ABSSSI 相关的大量当代细菌分离株(6222 株)具有很强的活性。