Zhanel George G, Baxter Melanie R, Adam Heather J, Sutcliffe Joyce, Karlowsky James A
Department of Medical Microbiology and Infectious Diseases, Max Rady College of Medicine, University of Manitoba, Winnipeg, R3E 0J9, Manitoba, Canada.
Department of Medical Microbiology and Infectious Diseases, Max Rady College of Medicine, University of Manitoba, Winnipeg, R3E 0J9, Manitoba, Canada.
Diagn Microbiol Infect Dis. 2018 May;91(1):55-62. doi: 10.1016/j.diagmicrobio.2017.12.013. Epub 2017 Dec 22.
Gram-negative (n=2213) and Gram-positive (n=2424) pathogens isolated from patients in 13 Canadian hospitals in 2014 and 2015 were tested for in vitro susceptibility to eravacycline and comparators using the Clinical and Laboratory Standards Institute broth microdilution method. The concentration of eravacycline inhibiting 90% of isolates (MIC) ranged from 0.5 to 2μg/mL for 9 species of Enterobacteriaceae tested (n=2067). Eravacycline activity was largely unaffected by extended-spectrum β-lactamase phenotypes in Escherichia coli (n=141) and Klebsiella pneumoniae (n=21). Eravacycline was active against Acinetobacter baumannii (n=28; MIC, 0.5μg/mL) and Stenotrophomonas maltophilia (n=118; MIC, 4μg/mL). Eravacycline MIC for staphylococci (n=1653), enterococci (n=289), and streptococci (n=482) ranged from 0.12 to 0.25, 0.06 to 0.12, and 0.015 to 0.06μg/mL, respectively. Eravacycline's potency was equivalent to or 2- to 4-fold greater than tigecycline against Enterobacteriaceae and Gram-positive cocci tested. Eravacycline demonstrates promising activity against recent clinical Gram-negative and Gram-positive bacteria, including multidrug-resistant pathogens.
2014年和2015年从加拿大13家医院的患者中分离出的革兰氏阴性菌(n = 2213)和革兰氏阳性菌(n = 2424),采用临床和实验室标准协会肉汤微量稀释法检测了对依拉环素及对照药物的体外敏感性。对于所检测的9种肠杆菌科细菌(n = 2067),抑制90%分离株的依拉环素浓度(MIC)范围为0.5至2μg/mL。在大肠杆菌(n = 141)和肺炎克雷伯菌(n = 21)中,依拉环素的活性在很大程度上不受超广谱β-内酰胺酶表型的影响。依拉环素对鲍曼不动杆菌(n = 28;MIC,0.5μg/mL)和嗜麦芽窄食单胞菌(n = 118;MIC,4μg/mL)具有活性。葡萄球菌(n = 1653)、肠球菌(n = 289)和链球菌(n = 482)的依拉环素MIC分别为0.12至0.25、0.06至0.12和0.015至0.06μg/mL。对于所检测的肠杆菌科细菌和革兰氏阳性球菌,依拉环素的效力等同于替加环素或比其高2至4倍。依拉环素对近期临床分离的革兰氏阴性菌和革兰氏阳性菌,包括多重耐药病原体,显示出有前景的活性。