Department of Internal Medicine, Division of Infectious Diseases, American University of Beirut Medical Center, P.O. Box 11-0236, Riad El-Solh, 1107 2020 Beirut, Lebanon.
Division of Medical Microbiology, Faculty of Health Sciences, University of Stellenbosch, Cape Town, South Africa; National Health Laboratory Service, Tygerberg Hospital, Cape Town, South Africa.
Int J Antimicrob Agents. 2014 Feb;43(2):170-8. doi: 10.1016/j.ijantimicag.2013.10.011. Epub 2013 Nov 15.
The Tigecycline Evaluation and Surveillance Trial (T.E.S.T.) was established in 2004 to monitor longitudinal changes in bacterial susceptibility to numerous antimicrobial agents, specifically tigecycline. In this study, susceptibility among Gram-positive and Gram-negative isolates between 2004 and 2011 from the Middle East and Africa was examined. Antimicrobial susceptibilities were determined using Clinical and Laboratory Standards Institute (CLSI) interpretive criteria, and minimum inhibitory concentrations (MICs) were determined by broth microdilution methods. US Food and Drug Administration (FDA)-approved breakpoints were used for tigecycline. In total, 2967 Gram-positive and 6322 Gram-negative isolates were examined from 33 participating centres. All Staphylococcus aureus isolates, including meticillin-resistant S. aureus, were susceptible to tigecycline, linezolid and vancomycin. Vancomycin, linezolid, tigecycline and levofloxacin were highly active (>97.6% susceptibility) against Streptococcus pneumoniae, including penicillin-non-susceptible strains. All Enterococcus faecium isolates were susceptible to tigecycline and linezolid, including 32 vancomycin-resistant isolates. Extended-spectrum β-lactamases were produced by 16.6% of Escherichia coli and 32.9% of Klebsiella pneumoniae. More than 95% of E. coli and Enterobacter spp. were susceptible to amikacin, tigecycline, imipenem and meropenem. The most active agents against Pseudomonas aeruginosa and Acinetobacter baumannii were amikacin (88.0% susceptible) and minocycline (64.2% susceptible), respectively; the MIC90 (MIC required to inhibit 90% of the isolates) of tigecycline against A. baumannii was low at 2mg/L. Tigecycline and carbapenem agents were highly active against most Gram-negative pathogens. Tigecycline, linezolid and vancomycin showed good activity against most Gram-positive pathogens from the Middle East and Africa.
替加环素评估和监测试验(T.E.S.T.)于 2004 年成立,旨在监测多种抗菌药物,特别是替加环素对细菌敏感性的纵向变化。在这项研究中,检查了 2004 年至 2011 年期间来自中东和非洲的革兰氏阳性和革兰氏阴性分离物的药敏性。使用临床和实验室标准协会(CLSI)解释标准确定抗菌药物敏感性,通过肉汤微量稀释法确定最小抑菌浓度(MIC)。替加环素使用美国食品和药物管理局(FDA)批准的折点。总共检查了来自 33 个参与中心的 2967 株革兰氏阳性和 6322 株革兰氏阴性分离物。所有金黄色葡萄球菌分离物,包括耐甲氧西林金黄色葡萄球菌,均对替加环素、利奈唑胺和万古霉素敏感。万古霉素、利奈唑胺、替加环素和左氧氟沙星对肺炎链球菌(包括青霉素不敏感株)具有高度活性(>97.6%的敏感性)。所有粪肠球菌分离物均对替加环素和利奈唑胺敏感,包括 32 株万古霉素耐药株。大肠埃希菌和肺炎克雷伯菌中分别有 16.6%和 32.9%产生超广谱β-内酰胺酶。超过 95%的大肠埃希菌和肠杆菌属对阿米卡星、替加环素、亚胺培南和美罗培南敏感。对铜绿假单胞菌和鲍曼不动杆菌最有效的药物分别是阿米卡星(88.0%敏感)和米诺环素(64.2%敏感);替加环素对鲍曼不动杆菌的 MIC90(抑制 90%分离物所需的 MIC)为 2mg/L,较低。替加环素和碳青霉烯类药物对大多数革兰氏阴性病原体具有高度活性。替加环素、利奈唑胺和万古霉素对来自中东和非洲的大多数革兰氏阳性病原体具有良好的活性。