JMI Laboratories, North Liberty, Iowa, USA.
University of Iowa, Iowa City, Iowa, USA.
Antimicrob Agents Chemother. 2020 Apr 21;64(5). doi: 10.1128/AAC.02488-19.
Omadacycline is a broad-spectrum aminomethylcycline approved in October 2018 by the U.S. Food and Drug Administration for treating acute bacterial skin and skin structure infections and community-acquired pneumonia as both an oral and intravenous once-daily formulation. In this report, the activities of omadacycline and comparators were tested against 49,000 nonduplicate bacterial isolates collected prospectively during 2016 to 2018 from medical centers in Europe (24,500 isolates, 40 medical centers [19 countries]) and the United States (24,500 isolates, 33 medical centers [23 states and all 9 U.S. census divisions]). Omadacycline was tested by broth microdilution following the methods in Clinical and Laboratory Standards Institute document M07 (, 11th ed., 2018). Omadacycline (MIC, 0.12/0.25 mg/liter) inhibited 98.6% of isolates at ≤0.5 mg/liter, including 96.3% of methicillin-resistant isolates and 99.8% of methicillin-susceptible isolates. Omadacycline potency was comparable for (MIC, 0.06/0.12 mg/liter), viridans group streptococci (MIC, 0.06/0.12 mg/liter), and beta-hemolytic streptococci (MIC, 0.12/0.25 mg/liter), regardless of species and susceptibility to penicillin, macrolides, or tetracycline. Omadacycline was active against all tested (MIC, 1/8 mg/liter; 87.5% of isolates were inhibited at ≤4 mg/liter) except (MIC, 16/>32 mg/liter) and indole-positive spp. (MIC, 8/32 mg/liter) and was most active against (MIC, 0.5/2 mg/liter), (MIC, 1/2 mg/liter), and spp. (MIC, 1/4 mg/liter). Omadacycline inhibited 92.4% of species complex and 88.5% of isolates at ≤4 mg/liter. Omadacycline was active against (MIC, 0.5/1 mg/liter), regardless of β-lactamase status, and against (MIC, ≤0.12/0.25 mg/liter). The potent activity of omadacycline against Gram-positive and -negative bacteria indicates that omadacycline merits further study in serious infections in which multidrug resistance and mixed Gram-positive and Gram-negative bacterial infections may be a concern.
奥马环素是一种广谱的氨甲基环素,于 2018 年 10 月获得美国食品和药物管理局批准,可用于治疗急性细菌性皮肤和皮肤结构感染和社区获得性肺炎,有口服和静脉注射的每日一次制剂。在本报告中,奥马环素及其对照药物的活性通过肉汤微量稀释法进行了测试,该方法遵循临床和实验室标准协会文件 M07(,第 11 版,2018 年)的方法。奥马环素(MIC,0.12/0.25μg/ml)在≤0.5μg/ml 时抑制了 98.6%的分离株,包括 96.3%的耐甲氧西林的分离株和 99.8%的甲氧西林敏感的分离株。奥马环素对 (MIC,0.06/0.12μg/ml)、草绿色链球菌(MIC,0.06/0.12μg/ml)和β-溶血性链球菌(MIC,0.12/0.25μg/ml)的效力相当,无论其对青霉素、大环内酯类或四环素的敏感性如何。奥马环素对所有测试的 (MIC,1/8μg/ml;87.5%的分离株在≤4μg/ml 时被抑制)都有效,除了 (MIC,16/>32μg/ml)和吲哚阳性 属。(MIC,8/32μg/ml),对 (MIC,0.5/2μg/ml)、 (MIC,1/2μg/ml)和 属。(MIC,1/4μg/ml)最为活跃。奥马环素抑制了 92.4%的 种复合体和 88.5%的 分离株,在≤4μg/ml 时。奥马环素对 (MIC,0.5/1μg/ml)有效,无论β-内酰胺酶状态如何,对 (MIC,≤0.12/0.25μg/ml)也有效。奥马环素对革兰氏阳性和阴性细菌的强大活性表明,奥马环素在严重感染中值得进一步研究,在这些感染中,可能存在多药耐药和混合革兰氏阳性和革兰氏阴性细菌感染的问题。