首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Characterization of Clinical Isolates of Klebsiella pneumoniae from 19 Laboratories Using the National Committee for Clinical Laboratory Standards Extended-Spectrum β-Lactamase Detection Methods
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Characterization of Clinical Isolates of Klebsiella pneumoniae from 19 Laboratories Using the National Committee for Clinical Laboratory Standards Extended-Spectrum β-Lactamase Detection Methods

机译:使用国家临床实验室标准委员会的广谱β-内酰胺酶检测方法表征19个实验室的肺炎克雷伯菌的临床分离株

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摘要

Extended-spectrum β-lactamases (ESBLs) are enzymes found in gram-negative bacilli that mediate resistance to extended-spectrum cephalosporins and aztreonam. In 1999, the National Committee for Clinical Laboratory Standards (NCCLS) published methods for screening and confirming the presence of ESBLs in Klebsiella pneumoniae, Klebsiella oxytoca, and Escherichia coli. To evaluate the confirmation protocol, we tested 139 isolates of K. pneumoniae that were sent to Project ICARE (Intensive Care Antimicrobial Resistance Epidemiology) from 19 hospitals in 11 U.S. states. Each isolate met the NCCLS screening criteria for potential ESBL producers (ceftazidime [CAZ] or cefotaxime [CTX] MICs were ≥2 μg/ml for all isolates). Initially, 117 (84%) isolates demonstrated a clavulanic acid (CA) effect by disk diffusion (i.e., an increase in CAZ or CTX zone diameters of ≥5 mm in the presence of CA), and 114 (82%) demonstrated a CA effect by broth microdilution (reduction of CAZ or CTX MICs by ≥3 dilutions). For five isolates, a CA effect could not be determined initially by broth microdilution because of off-scale CAZ results. However, a CA effect was observed in two of these isolates by testing cefepime and cefepime plus CA. The cefoxitin MICs for 23 isolates that failed to show a CA effect by broth microdilution were ≥32 μg/ml, suggesting either the presence of an AmpC-type β-lactamase or porin changes that could mask a CA effect. By isoelectric focusing (IEF), 7 of the 23 isolates contained a β-lactamase with a pI of ≥8.3 suggestive of an AmpC-type β-lactamase; 6 of the 7 isolates were shown by PCR to contain both ampC-type and blaOXA genes. The IEF profiles of the remaining 16 isolates showed a variety of β-lactamase bands, all of which had pIs of ≤7.5. All 16 isolates were negative by PCR with multiple primer sets for ampC-type, blaOXA, and blaCTX-M genes. In summary, 83.5% of the K. pneumoniae isolates that were identified initially as presumptive ESBL producers were positive for a CA effect, while 5.0% contained β-lactamases that likely masked the CA effect. The remaining 11.5% of the isolates studied contained β-lactamases that did not demonstrate a CA effect. An algorithm based on phenotypic analyses is suggested for evaluation of such isolates.
机译:广谱β-内酰胺酶(ESBLs)是在革兰氏阴性杆菌中发现的酶,介导对广谱头孢菌素和氨曲南的耐药性。 1999年,美国国家临床实验室标准委员会(NCCLS)发布了筛选和确认肺炎克雷伯菌,产氧克雷伯菌和大肠杆菌中ESBLs的方法。为了评估确认协议,我们测试了139株肺炎克雷伯菌的分离株,这些菌株已从美国11个州的19家医院发送到了ICARE项目(重症监护抗菌素耐药性流行病学)。每个分离株均符合潜在ESBL生产者的NCCLS筛选标准(所有分离株的头孢他啶[CAZ]或头孢噻肟[CTX] MIC≥2μg/ ml)。最初,有117(84%)的分离物通过盘扩散表现出棒酸(CA)的作用(即在存在CA的情况下,CAZ或CTX区直径增加≥5 mm),而114(82%)的分离物表现出CA肉汤微稀释(通过≥3种稀释减少CAZ或CTX MIC)的效果。对于五个分离株,由于规模不大的CAZ结果,最初无法通过肉汤微量稀释来确定CA效果。但是,通过测试头孢吡肟和头孢吡肟加CA,在其中的两个分离物中观察到了CA效应。未能通过肉汤微量稀释显示出CA效应的23个分离物的头孢西丁MIC≥32μg/ ml,表明存在AmpC型β-内酰胺酶或孔蛋白的变化可能掩盖了CA效应。通过等电聚焦(IEF),这23种分离物中的7种含有β-内酰胺酶,其pI≥8.3暗示了AmpC型β-内酰胺酶。通过PCR显示,在7个分离物中,有6个同时含有ampC型和blaOXA基因。其余16个分离株的IEF图谱显示各种β-内酰胺酶带,所有带的pI≤7.5。通过针对ampC型,blaOXA和blaCTX-M基因的多个引物对,所有16个分离株均为阴性。总之,最初被鉴定为ESBL产生者的肺炎克雷伯菌分离株中有83.5%对CA效应呈阳性,而5.0%的β-内酰胺酶可能掩盖了CA效应。剩余的11.5%的分离株含有未证明CA作用的β-内酰胺酶。建议基于表型分析的算法来评估这种分离株。

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