JMI Laboratories, North Liberty, IA, USA.
JMI Laboratories, North Liberty, IA, USA.
Diagn Microbiol Infect Dis. 2014 Apr;78(4):449-56. doi: 10.1016/j.diagmicrobio.2014.01.003. Epub 2014 Jan 14.
Ceftaroline-avibactam and comparator agents were tested against clinical isolates collected at 174 medical centers from patients with acute bacterial skin and skin structure infection (ABSSSI) in the United States (USA) during 2010-2012. Isolates were processed at the medical centers and forwarded to a central laboratory for confirmatory identification and susceptibility testing using reference methods. Ceftaroline-avibactam was highly active against methicillin-susceptible (MIC50/90, 0.25/0.25 μg/mL) and methicillin-resistant Staphylococcus aureus (MRSA; MIC50/90, 0.5/1 μg/mL). Vancomycin, tigecycline, daptomycin, and linezolid were also active (>99.9% susceptible) against MRSA (51.4% of S. aureus), but activity against MRSA was decreased for erythromycin, levofloxacin, and clindamycin (10.8, 40.3, and 81.9% susceptible, respectively). β-Hemolytic streptococci were highly susceptible to β-lactam antimicrobials, including ceftaroline-avibactam (MIC50/90, ≤0.03/≤0.03 μg/mL). Ceftaroline-avibactam was very active against Escherichia coli and Klebsiella pneumoniae (MIC50/90, 0.03/0.06 and 0.06/0.25 μg/mL, respectively) including extended-spectrum β-lactamase (ESBL) screen-positive phenotypes (MIC50/90, 0.06/0.12 and 0.12/1 μg/mL, respectively). Susceptibility of ESBL screen-positive E. coli and K. pneumoniae was 100.0/97.9% for tigecycline and 99.2/56.1% for meropenem, respectively. Susceptibility to other agents for ESBL screen-positive E. coli and K. pneumoniae was decreased. Ceftaroline-avibactam exhibited a broad-spectrum of in vitro activity against isolates from patients in the USA with ABSSSI including MRSA, β-hemolytic streptococci, E. coli, and K. pneumoniae as well as ESBL screen-positive phenotype isolates and merits further study in clinical indications where these resistant organisms may be a concern.
头孢洛林-阿维巴坦和对照药物对来自美国(USA)174 家医疗中心的 174 家医疗中心的急性细菌性皮肤和皮肤结构感染(ABSSSI)患者的临床分离株进行了测试。分离株在医疗中心进行处理,并送到一个中央实验室,使用参考方法进行确认鉴定和药敏试验。头孢洛林-阿维巴坦对甲氧西林敏感(MIC50/90,0.25/0.25μg/ml)和耐甲氧西林金黄色葡萄球菌(MRSA;MIC50/90,0.5/1μg/ml)具有高度活性。万古霉素、替加环素、达托霉素和利奈唑胺对 MRSA(51.4%金黄色葡萄球菌)也具有活性(99.9%敏感),但对红霉素、左氧氟沙星和克林霉素的活性降低(分别为 10.8%、40.3%和 81.9%敏感)。β-溶血性链球菌对包括头孢洛林-阿维巴坦在内的β-内酰胺类抗菌药物高度敏感(MIC50/90,≤0.03/≤0.03μg/ml)。头孢洛林-阿维巴坦对大肠埃希菌和肺炎克雷伯菌(MIC50/90,0.03/0.06 和 0.06/0.25μg/ml)非常活跃,包括扩展谱β-内酰胺酶(ESBL)筛选阳性表型(MIC50/90,0.06/0.12 和 0.12/1μg/ml)。ESBL 筛选阳性大肠埃希菌和肺炎克雷伯菌对替加环素的敏感性为 100.0/97.9%,对美罗培南的敏感性为 99.2/56.1%。ESBL 筛选阳性大肠埃希菌和肺炎克雷伯菌对其他药物的敏感性降低。头孢洛林-阿维巴坦对来自美国 ABSSSI 患者的分离株具有广谱的体外活性,包括耐甲氧西林金黄色葡萄球菌、β-溶血性链球菌、大肠埃希菌和肺炎克雷伯菌以及 ESBL 筛选阳性表型分离株,值得在这些耐药菌可能成为关注点的临床适应症中进一步研究。