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Fourier-Transform InfraRed Spectroscopy Can Quickly Type Gram-Negative Bacilli Responsible for Hospital Outbreaks

机译:傅里叶变换红外光谱可以快速键入革兰氏阴性杆菌应对医院爆发

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摘要

The typing of epidemic bacterial pathogens in hospitals relies on DNA-based, expensive, and time-consuming techniques, that are often limited to retrospective studies. However, the quick identification of epidemic pathogens in the routine of the microbiology laboratories would expedite infection control procedures that limit the contamination of new patients. IR Biotyper (Bruker Daltonics GmbH) is a new typing machine based on Fourier-transform infrared (FTIR) spectroscopy which generates spectra, aiming at typing the micro-organisms within 3 h. This technique discriminates the isolates by exploring the differences of the surface cell polysaccharides. In this work, we evaluated the ability of the FTIR spectroscopy to recognize Gram-negative bacilli clones responsible for hospital outbreaks. Isolates of Pseudomonas aeruginosa (n = 100), Klebsiella pneumoniae (n = 16), Enterobacter cloacae (n = 23), and Acinetobacter baumannii (n = 20) were typed by the reference methods Multi-Locus Sequence Typing (defining sequence types – STs) along with or without pulsed field gel electrophoresis (PFGE) (defining pulsotypes), and by FTIR spectroscopy. The congruence of FTIR spectroscopy clustering was compared to those of MLST and PFGE by Adjusted Rand index and Adjusted Wallace coefficient. We found that FTIR spectroscopy accurately clustered P. aeruginosa, K. pneumoniae, and E. cloacae isolates belonging to the same ST. The performance of the FTIR spectroscopy was slightly lower for A. baumannii. Furthermore, FTIR spectroscopy also correctly clustered P. aeruginosa isolates having a similar pulsotype. Overall, the IR Biotyper can quickly (in less than 3 h) detect the spread of clones of P. aeruginosa, K. pneumoniae, E. cloacae, and A. baumannii. The use of this technique by clinical microbiology laboratories may help to tackle the spread of epidemic clones by the quick implementation of infection control measures.
机译:医院中流行细菌病原体的类型取决于基于DNA的昂贵且耗时的技术,而这些技术通常仅限于回顾性研究。但是,在微生物实验室常规中快速识别流行病原体将加快感染控制程序,从而限制了新患者的污染。 IR Biotyper(Bruker Daltonics GmbH)是一种基于傅立叶变换红外(FTIR)光谱学的新型打字机,其产生光谱,旨在在3小时内对微生物进行打字。该技术通过探索表面细胞多糖的差异来区分分离株。在这项工作中,我们评估了FTIR光谱法识别引起医院暴发的革兰氏阴性杆菌克隆的能力。铜绿假单胞菌(n = 100),肺炎克雷伯菌(n = 16),阴沟肠杆菌(n = 23)和鲍曼不动杆菌(n = 20)的分离株通过参考方法多基因座序列分型(定义序列类型– STs)结合或不结合脉冲场凝胶电泳(PFGE)(定义脉冲型)和FTIR光谱。通过调整兰德指数和调整华莱士系数,将FTIR光谱聚类的一致性与MLST和PFGE的一致性进行了比较。我们发现FTIR光谱准确地将属于同一ST的铜绿假单胞菌,肺炎克雷伯菌和阴沟肠杆菌分离物聚类。鲍曼不动杆菌的FTIR光谱性能稍低。此外,FTIR光谱学还正确地聚集了具有相似脉冲型的铜绿假单胞菌分离物。总体而言,IR Biotyper可以快速(不到3小时)检测铜绿假单胞菌,肺炎克雷伯菌,阴沟肠杆菌和 A克隆的扩散。鲍曼氏菌。临床微生物实验室使用此技术可通过快速实施感染控制措施来帮助解决流行性克隆的传播。

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