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Development and application of an oligonucleotide microarray and real-time quantitative PCR for detection of wastewater bacterial pathogens

机译:寡核苷酸微阵列和实时定量PCR技术在废水细菌病原体检测中的开发与应用

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Conventional microbial water quality test methods are well known for their technical limitations, such as lack of direct pathogen detection capacity and low throughput capability. The microarray assay has recently emerged as a promising alternative for environmental pathogen monitoring. In this study, bacterial pathogens were detected in municipal wastewater using a microarray equipped with short oligonucleotide probes targeting 16S rRNA sequences. To date, 62 probes have been designed against 38 species, 4 genera, and 1 family of pathogens. The detection sensitivity of the microarray for a waterbome pathogen Aeromonas hydrophila was determined to be approximately 1.0% of the total DNA, or approximately 10~3 A. hydrophila cells per sample. The efficacy of the DNA microarray was verified in a parallel study where pathogen genes and E. coli cells were enumerated using realtime quantitative PCR (qPCR) and standard membrane filter techniques, respectively. The microarray and qPCR successfully detected multiple wastewater pathogen species at different stages of the disinfection process (i.e. secondary effluents vs. disinfected final effluents) and at two treatment plants employing different disinfection methods (i.e. chlorination vs. UV irradiation). This result demonstrates the effectiveness of the DNA microarray as a semi-quantitative, high throughput pathogen monitoring tool for municipal wastewater.
机译:常规微生物水质测试方法因其技术局限性而众所周知,例如缺乏直接的病原体检测能力和低通量能力。最近,微阵列测定法已成为环境病原体监测的有希望的替代方法。在这项研究中,使用配备了针对16S rRNA序列的短寡核苷酸探针的微阵列,在市政废水中检测了细菌病原体。迄今为止,已针对38种,4属和1个病原体家族设计了62个探针。经测定,微阵列对水生病原体嗜水气单胞菌的检测灵敏度约为总DNA的1.0%,或每个样品约占10〜3个嗜水气单胞菌细胞。在一项平行研究中验证了DNA微阵列的功效,该研究分别使用实时定量PCR(qPCR)和标准膜过滤技术对病原体基因和大肠杆菌细胞进行了计数。芯片和qPCR成功地在消毒过程的不同阶段(即次要废水与已消毒的最终废水)以及两个采用不同消毒方法(即氯化与UV辐射)的处理厂成功检测了多种废水病原体。该结果证明了DNA微阵列作为用于城市废水的半定量,高通量病原体监测工具的有效性。

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