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首页> 外文期刊>Journal of Clinical Microbiology >Evaluation of the Bruker MALDI Biotyper for Identification of Fastidious Gram-Negative Rods
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Evaluation of the Bruker MALDI Biotyper for Identification of Fastidious Gram-Negative Rods

机译:布鲁克MALDI生物分型仪用于鉴定革兰氏阴性杆的评估

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摘要

Matrix-assisted laser desorption ionization?time of flight mass spectrometry (MALDI-TOF MS) has entered clinical laboratories, facilitating identification of bacteria. Here, we evaluated the MALDI Biotyper (Bruker Daltonics) for the identification of fastidious Gram-negative rods (GNR). Three sample preparation methods, direct colony transfer, direct transfer plus on-target formic acid preparation, and ethanol-formic acid extraction, were analyzed for 151 clinical isolates. Direct colony transfer applied with the manufacturer's interpretation criteria resulted in overall species and genus identification rates of 43.0% and 32.5%, respectively; 23.2% of the isolates were not identified, and two misidentifications (1.3%) were observed. The species identification rates increased to 46.4% and 53.7% for direct transfer plus formic acid preparation and ethanol-formic acid extraction, respectively. In addition, we evaluated score value cutoff alterations. The identification rates hardly increased by reducing the genus cutoff, while reducing the 2.0 species cutoff to 1.9 and to 1.8 increased the identification rates to up to 66.2% without increasing the rate of misidentifications. This study shows that fastidious GNR can reliably be identified using the MALDI Biotyper. However, the identification rates do not reach those of nonfastidious GNR such as the Enterobacteriaceae. In addition, two approaches optimizing the identification of fastidious GNR by the MALDI Biotyper were demonstrated: formic acid-based on-target sample treatment and reductions in cutoff scores to increase the species identification rates.
机译:基质辅助激光解吸电离飞行时间质谱仪(MALDI-TOF MS)已进入临床实验室,有助于细菌鉴定。在这里,我们评估了MALDI Biotyper(Bruker Daltonics),以鉴定难检的革兰氏阴性棒(GNR)。分析了151种临床分离株的三种样品制备方法,即直接菌落转移,直接转移加目标甲酸制备和乙醇-甲酸提取。按照制造商的解释标准进行的直接菌落转移导致总体物种和属识别率分别为43.0%和32.5%;未鉴定出23.2%的分离物,观察到两个错误鉴定结果(1.3%)。直接转移加甲酸制备和乙醇-甲酸萃取的物种识别率分别提高到46.4%和53.7%。此外,我们评估了得分值的临界值变化。通过减少属截止值,识别率几乎不会增加,而将2.0物种截止值减少到1.9和1.8则可以将识别率提高到66.2%,而不会增加错误识别率。这项研究表明,可以使用MALDI Biotyper可靠地识别出挑剔的GNR。但是,鉴定率不能达到肠胃菌科等非苛刻GNR的鉴定率。此外,还展示了两种通过MALDI Biotyper优化对伪劣GNR的鉴定的方法:基于甲酸的目标样品处理和降低截留分数以提高物种鉴定率。

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