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Five-Year Summary of In Vitro Activity and Resistance Mechanisms of Linezolid against Clinically Important Gram-Positive Cocci in the United States from the LEADER Surveillance Program (2011 to 2015)

机译:从领导监督计划(2011年到2015年)中美国对美国临床重要革兰氏阳性Cocci进行临床上重要革兰氏阳性Coccc的五年综述

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This report describes linezolid susceptibility testing results for 6,741 Gram-positive pathogens from 60 U. S. sites collected during 2015 for the LEADER Program. In addition, the report summarizes linezolid in vitro activity, resistance mechanisms, and molecular typing obtained for 2011 to 2015. During 2015, linezolid showed potent activity in testing against Staphylococcus aureus, inhibiting >99.9% of 3,031 isolates at <= 2 mu g/ml. Similarly, linezolid showed coverage against 99.2% of coagulase-negative staphylococci, 99.7% of enterococci, and 100.0% of Streptococcus pneumoniae, virdans group, and beta-hemolytic streptococcus isolates tested. The overall linezolid resistance rate remained a modest <1% from 2011 to 2015. Staphylococci, especially Staphylococcus epidermidis, showed a range of linezolid resistance mechanisms. Increased annual trends for the presence of cfr among Staphylococcus aureus isolates were not observed, but 64.3% (9/14) of the isolates with decreased susceptibility (MIC, >= 4 mu g/ml) to linezolid carried this transferrable gene (2011 to 2015). The cfr gene was detected in 21.9% (7/32) of linezolid-resistant staphylococci other than S. aureus from 2011 to 2015. The optrA gene was noted in half (2/4) of the population of linezolid-nonsusceptible Enterococcus faecalis isolates from 2011 to 2015, while linezolid-nonsusceptible Enterococcus faecium isolates showed alterations predominantly (16/16) in the 23S rRNA gene (G2576T). This report confirms a long record of linezolid activity against Gram-positive isolates in the United States since regulatory approval in 2000 and reports the oxazolidinones evolving resistance mechanisms.
机译:本报告描述了6,741克阳性病原体的LINEzolid易感性测试结果,从2015年收集的60美元占领了6,741克阳性病原体。此外,该报告总结了LIMIZOLID在2011年至2015年获得的体外活性,抗性机制和分子类型。在2015年期间,LINEZOLID在对金黄色葡萄球菌进行测试时表现出有效的活性,抑制> 99.9%的3,031个分离物在<=2μg/ ml。类似地,LINEZOLID显示覆盖率覆盖99.2%的凝固酶阴性葡萄球菌,99.7%的肠球菌,肺炎链球菌的100.0%,virdans组和β-溶血性链球菌分离物。从2011年至2015年,总滴斑抗性率仍然是一种温和的<1%。葡萄球菌,尤其是葡萄球菌表皮,表现出一系列线状抗性机制。未观察到金黄色葡萄球菌中的CFR中的CFR存在的年度趋势,但具有降低的敏感性(MIC,> =4μg/ ml)对Linezolid的64.3%(9/14)分离株携带该转移基因(2011至2015)。在2011至2015年的金黄色葡萄球菌以外的21.9%(7/32)中检测到CFR基因。OPTra基因已注意到线唑胺 - 非肌瘤粪便分离株的一半(2/4)从2011年到2015年,虽然LINEzolid-nonscorpible肠球菌粪便分离物在23s rRNA基因(G2576T)中主要显示出改变(16/16)。本报告证实,自2000年监管批准以来,对美国革兰氏阳性孤立的LINZOLID活动进行了长期记录,并报告了恶唑烷酮的抗性机制。

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