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首页> 外文期刊>Emerging Infectious Diseases >Antimicrobial Susceptibility Breakpoints and First-Step parC Mutations in Streptococcus pneumoniae: Redefining Fluoroquinolone Resistance
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Antimicrobial Susceptibility Breakpoints and First-Step parC Mutations in Streptococcus pneumoniae: Redefining Fluoroquinolone Resistance

机译:肺炎链球菌的抗生素敏感性起点和第一步parC突变:重新定义氟喹诺酮耐药性

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Clinical antimicrobial susceptibility breakpoints areused to predict the clinical outcome of antimicrobial treat-ment. In contrast, microbiologic breakpoints are used toidentify isolates that may be categorized as susceptiblewhen applying clinical breakpoints but harbor resistancemechanisms that result in their reduced susceptibility to theagent being tested. Currently, the National Committee forClinical Laboratory Standards (NCCLS) guidelines utilizeclinical breakpoints to characterize the activity of the fluoro-quinolones against Streptococcus pneumoniae. To deter-mine whether levofloxacin breakpoints can identify isolatesthat harbor recognized resistance mechanisms, we exam-ined 115 S. pneumoniae isolates with a levofloxacin MIC of>2 μg/mL for first-step parC mutations. A total of 48 (59%)of 82 isolates with a levofloxacin MIC of 2 μg/mL, a levelconsidered susceptible by NCCLS criteria, had a first-stepmutation in parC. Whether surveillance programs that uselevofloxacin data can effectively detect emerging resist-ance and whether fluoroquinolones can effectively treatinfections caused by such isolates should be evaluated
机译:临床抗菌药敏感性断点用于预测抗菌药物治疗的临床结果。相反,微生物断点用于鉴定在应用临床断点时可能被归类为易感菌株,但具有导致其对被测试剂敏感性降低的耐药机制。目前,美国国家临床实验室标准委员会(NCCLS)指南利用临床断点来表征氟喹诺酮类药物对肺炎链球菌的活性。为了确定左氧氟沙星的断点是否可以识别出具有公认抗性机制的分离株,我们对第一步parC突变的115株左氧氟沙星MIC≥2μg/ mL的肺炎链球菌进行了检查。 82株分离出的左氧氟沙星MIC为2μg/ mL(根据NCCLS标准易感的水平)的菌株中,共有48株(59%)在parC中发生了第一步突变。应该评估使用左氧氟沙星数据的监测程序是否可以有效检测新出现的耐药性,以及氟喹诺酮类药物是否可以有效治疗此类分离物引起的感染

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