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Bacteriophage Amplification-Coupled Detection and Identification of Bacterial Pathogens

机译:噬菌体扩增偶联的细菌病原体的检测和鉴定

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Current methods of species-specific bacterial detection and identification are complex, time-consuming, and often require expensive specialized equipment and highly trained personnel. Numerous biochemical and genotypic identification methods have been applied to bacterial characterization, but all rely on tedious microbiological culturing practices and/or costly sequencing protocols which render them impractical for deployment as rapid, cost-effective point-of-care or field detection and identification methods. With a view towards addressing these shortcomings, we have exploited the evolutionarily conserved interactions between a bacteriophage (phage) and its bacterial host to develop species-specific detection methods. Phage amplification-coupled matrix assisted laser desorption time-of-flight mass spectrometry (MALDI-TOF-MS) was utilized to rapidly detect phage propagation resulting from species-specific in vitro bacterial infection. This novel signal amplification method allowed for bacterial detection and identification in as little as 2 h, and when combined with disulfide bond reduction methods devel-oped in our laboratory to enhance MALDI-TOF-MS resolution, was observed to lower the limit of detection by several orders of magnitude over conventional spectroscopy and phage typing methods. Phage amplification has been combined with lateral flow immunochromatography (LFI) to develop rapid, easy-to-operate, portable, species-specific point-of-care (POC) detection devices. Prototype LFI detectors have been developed and characterized for Yersinia pestis and Bacillus anthracis, the etiologic agents of plague and anthrax, respectively. Comparable sensitivity and rapidity was observed when phage amplification was adapted to a species-specific handheld LFI detector, thus allowing for rapid, simple, POC bacte-rial detection and identification while eliminating the need for bacterial culturing or DNA isolation and amplification techniques.
机译:目前的物种特异性细菌检测和识别方法复杂,耗时,并且通常需要昂贵的专业设备和高度培训的人员。许多生化和基因型鉴定方法已应用于细菌性表征,但所有依赖于繁琐的微生物培养实践和/或昂贵的测序方案,使其成为迅速,经济高效的护理点或现场检测和识别方法的不切实际。 。为了解决这些缺点,我们利用了噬菌体(噬菌体)和其细菌宿主之间的进化保守相互作用来开发物种特异性检测方法。噬菌体扩增偶联的基质辅助激光解吸飞行时间质谱(MALDI-TOF-MS)以快速检测由特异性体外细菌感染产生的噬菌体繁殖。这种新的信号放大方法允许细菌检测和鉴定只要在2小时内,并且当与在我们实验室中的二硫键还原方法结合在我们的实验室中加强MALDI-TOF-MS分辨率时,以降低检测极限常规光谱和噬菌体键入方法的几个数量级。噬菌体扩增已与横向流动免疫层析(LFI)组合,以开发快速,易于操作,便携式的物种特异性护理点(POC)检测装置。原型LFI探测器已经开发并表征了鉴于鉴赏和杆菌,分别是瘟疫和炭疽病的病因因子。当噬菌体扩增适用于特定的手持式LFI检测器时,观察到可比灵敏度和快速性,从而允许快速,简单,PoC Bacte-Rial检测和鉴定,同时消除了细菌培养或DNA分离和扩增技术的需要。

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