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Evaluation of a microfluidic chip system for preparation of bacterial DNA from swabs air and surface water samples

机译:评价用于从拭子空气和地表水样品中制备细菌DNA的微流控芯片系统

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摘要

The detection of bacterial pathogens from complex sample matrices by PCR requires efficient DNA extraction. In this study, a protocol for extraction and purification of DNA from swabs, air, and water samples using a microfluidic chip system was established. The optimized protocol includes a combination of thermal, chemical and enzymatic lysis followed by chip-based DNA purification using magnetic particles. The procedure was tested using Gram-positive Bacillus thuringiensis Berliner var. kurstaki as a model organism for Bacillus anthracis and the attenuated live vaccine strain of Francisella tularensis subsp. holarctica as Gram-negative bacterium. The detection limits corresponded to 103 genome equivalents per milliliter (GE/ml) for surface water samples spiked with F. tularensis and 102 GE/ml for B. thuringiensis. In air, 10 GE of F. tularensis per 10 L and 1 GE of B. thuringiensis per 10 L were detectable. For swab samples obtained from artificially contaminated surfaces the detection limits were 4 × 103 GE/cm2 for F. tularensis and 4 × 102 GE/cm2 for B. thuringiensis. Suitability of the chip-assisted procedure for DNA preparation of real samples was demonstrated using livestock samples. The presence of thermophilic Campylobacter spp. DNA could be confirmed in air samples collected on pig and broiler farms.
机译:通过PCR从复杂样品基质中检测细菌病原体需要有效的DNA提取。在这项研究中,建立了使用微流控芯片系统从拭子,空气和水样品中提取和纯化DNA的协议。优化的方案包括热裂解,化学裂解和酶裂解的组合,然后使用磁性颗粒进行基于芯片的DNA纯化。使用革兰氏阳性苏云金芽孢杆菌Berliner var测试该程序。 kurstaki是炭疽芽孢杆菌和土拉弗朗西斯菌亚种减毒活疫苗株的模型生物。幽门螺杆菌作为革兰氏阴性细菌。检测限对应于加标杜氏杆菌的地表水样品每毫升10 3 基因组当量(GE / ml)和苏云金芽孢杆菌10 2 GE / ml。在空气中,每10升可检测到10 GE的图莱特氏菌和每10升可检测到1 GE的苏云金芽孢杆菌。从人工污染的表面获取的拭子样品的检测极限为土拉弗朗西斯菌为4×10 3 GE / cm 2 和4×10 2 苏云金芽孢杆菌GE / cm 2 使用牲畜样品证明了芯片辅助程序用于制备真实样品的DNA的适用性。嗜热弯曲杆菌属的存在。可以从养猪场和肉鸡场收集的空气样本中确认DNA。

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