JMI Laboratories, North Liberty, IA 52317, USA.
Diagn Microbiol Infect Dis. 2012 Sep;74(1):54-61. doi: 10.1016/j.diagmicrobio.2012.05.012. Epub 2012 Jun 15.
The LEADER program monitors the in vitro activity of linezolid and comparator agents across the United States using reference broth microdilution and supportive molecular susceptibility-based investigations. This report summarizes the data from the 2010 program, the seventh consecutive year. A total of 61 medical centers from the USA including 7 medical centers specializing in children's healthcare provided a total of 6801 Gram-positive pathogens. The medical centers represented all 9 US Bureau of Census geographic regions. The organisms tested by reference broth microdilution were 3105 Staphylococcus aureus, 944 coagulase-negative staphylococci (CoNS), 934 Enterococci, 803 Streptococcus pneumoniae, 604 β-haemolytic streptococci, and 411 viridans group and other streptococci. The MIC(90) value for each of the above 6 targeted groups of organisms was 1 μg/mL. The "all organism" linezolid-resistant and nonsusceptible rate was 0.38%, which has been constant at 0.34% (2009) to 0.45% (2006) for the last 4 years. For Staphylococcus aureus, only 0.06% of the isolates were linezolid-resistant (MIC, ≥8 μg/mL); however, 2 additional methicillin-resistant Staphylococcus aureus had a cfr and a MIC of only 4 μg/mL. Resistance to linezolid was detected in 7 enterococci (0.75%) and 14 CoNS isolates (1.48%). This also represents a stable rate of resistance noted since the 2006 LEADER program report. Of note, for the first time in the 7 years of the Leader Program a linezolid-resistant Streptococcus pneumoniae was encountered. Overall, the results of the LEADER program demonstrate that linezolid maintains excellent in vitro activity against target Gram-positive pathogens across the USA. The LEADER program continues to provide valuable reference and molecular-level monitoring of linezolid activity.
LEADER 项目通过参考肉汤微量稀释法和支持性基于分子药敏的研究在美国监测利奈唑胺和对照药物的体外活性。本报告总结了 2010 年项目的数据,这是连续第七年报告。来自美国的 61 个医疗中心,包括 7 个专门从事儿童保健的医疗中心,共提供了 6801 株革兰阳性病原体。这些医疗中心代表了美国人口普查局的所有 9 个地理区域。通过参考肉汤微量稀释法进行测试的微生物包括 3105 株金黄色葡萄球菌、944 株凝固酶阴性葡萄球菌(CoNS)、934 株肠球菌、803 株肺炎链球菌、604 株β-溶血性链球菌和 411 株草绿色链球菌和其他链球菌。上述 6 个目标微生物群的 MIC90 值均为 1 μg/ml。所有微生物的利奈唑胺耐药和不敏感率为 0.38%,自 2006 年以来,该比例一直稳定在 0.34%(2009 年)至 0.45%(2006 年)之间。金黄色葡萄球菌中,只有 0.06%的分离株对利奈唑胺耐药(MIC≥8μg/ml);然而,另外 2 株耐甲氧西林金黄色葡萄球菌的 cfr 和 MIC 仅为 4μg/ml。利奈唑胺耐药性在 7 株肠球菌(0.75%)和 14 株 CoNS 分离株(1.48%)中被检测到。这也代表了自 2006 年 LEADER 项目报告以来一直稳定的耐药率。值得注意的是,LEADER 项目在 7 年的运行过程中首次遇到了耐利奈唑胺的肺炎链球菌。总体而言,LEADER 项目的结果表明,利奈唑胺在美国对目标革兰阳性病原体保持着极好的体外活性。LEADER 项目继续为利奈唑胺的活性提供有价值的参考和分子水平监测。