Department of Laboratory Medicine, Karolinska Institute, Karolinska University Hospital Huddinge, Stockholm, Sweden.
Antimicrob Agents Chemother. 2010 May;54(5):1811-4. doi: 10.1128/AAC.01716-09. Epub 2010 Mar 15.
Ceftaroline is a new broad-spectrum cephalosporin being developed for the treatment of serious bacterial infections, including those caused by aerobic Gram-positive and Gram-negative bacteria. The purpose of the present study was to investigate the effect of administration of ceftaroline on the intestinal flora of healthy subjects. Twelve healthy subjects (6 males and 6 females), 20 to 41 years of age, received ceftaroline (600 mg) by intravenous infusion every 12 h (q12h) for 7 days. Plasma and feces were collected for determination of ceftaroline concentration and analysis of fecal flora. Fecal specimens were cultured on nonselective and selective media. Different colony types were counted, isolated in pure culture, and identified to the genus level. All new strains of colonizing bacteria were tested for susceptibility to ceftaroline. The concentrations of ceftaroline in plasma were as follows: on day 2, 17.5 to 34.8 mg/liter; on day 5, 19.7 to 33.2 mg/liter; and on day 7, 18.0 to 29.8 mg/liter. No ceftaroline concentrations were found on day -1, 9, 14, or 21. No measurable concentrations in feces were found on day -1, 2, 5, 7, 9, 14, or 21. There was a minor impact on the numbers of Escherichia coli strains, while the numbers of enterococci and Candida albicans strains were not affected. There were moderate decreases in the numbers of bifidobacteria and lactobacilli during the first 7 days, while the numbers of clostridia increased during the same period. No impact on the numbers of Bacteroides bacteria was noticed. No new colonizing aerobic or anaerobic bacteria resistant to ceftaroline (MIC >or= 4 mg/liter) were found. Ceftaroline had no significant ecological impact on the human intestinal microflora.
头孢洛林是一种新的广谱头孢菌素,正在开发用于治疗严重的细菌感染,包括由需氧革兰阳性和革兰阴性细菌引起的感染。本研究的目的是研究头孢洛林给药对健康受试者肠道菌群的影响。12 名健康受试者(6 名男性和 6 名女性),年龄 20 至 41 岁,每 12 小时(q12h)静脉输注头孢洛林(600mg)一次,连续 7 天。采集血浆和粪便样本以测定头孢洛林浓度并分析粪便菌群。粪便标本接种于非选择性和选择性培养基。计数不同的菌落类型,分离纯培养物,并鉴定到属水平。对所有定植细菌的新菌株进行头孢洛林敏感性测试。血浆中头孢洛林的浓度如下:第 2 天,17.5 至 34.8mg/L;第 5 天,19.7 至 33.2mg/L;第 7 天,18.0 至 29.8mg/L。第-1 天、第 9 天、第 14 天和第 21 天未检测到头孢洛林浓度。第-1 天、第 2 天、第 5 天、第 7 天、第 9 天、第 14 天和第 21 天粪便中未检测到可测量的浓度。大肠杆菌菌株数量略有减少,而肠球菌和白色念珠菌菌株数量不受影响。双歧杆菌和乳酸杆菌数量在前 7 天内适度减少,而梭菌数量在同一时期增加。未发现拟杆菌数量受到影响。未发现对头孢洛林(MIC≥4mg/L)耐药的新定植需氧或厌氧细菌。头孢洛林对人类肠道微生物群没有显著的生态影响。