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首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >Propidium monoazide-quantitative polymerase chain reaction for viable Escherichia coli and Pseudomonas aeruginosa detection from abundant background microflora
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Propidium monoazide-quantitative polymerase chain reaction for viable Escherichia coli and Pseudomonas aeruginosa detection from abundant background microflora

机译:从丰富的背景微生物区系中检测单叠氮化丙锭定量聚合酶链反应以检测活的大肠杆菌和铜绿假单胞菌

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摘要

Nucleic acid-based techniques represent a promising alternative to cultivation-based microbial water quality assessment methods. However, their application is hampered by their innate inability to differentiate between living and dead organisms. Propidium monoazide (PMA) treatment was proposed as an efficient approach for alleviating this limitation. In this study, we demonstrate the performance of PMA-quantitative polymerase chain reaction (qPCR) for the detection of indicator organisms (Escherichia coli and Pseudomonas aeruginosa) in a background of a highly abundant and complex microflora. Treatment with 10 μM PMA resulted in the complete or significant reduction of the false positive signal arising from the amplification of DNA from dead cells.
机译:基于核酸的技术代表了一种基于栽培的微生物水质评估方法的有前途的替代方法。但是,它们的应用因其固有的无法区分活体和死生物的能力而受到阻碍。提出了单叠氮化丙锭(PMA)处理作为减轻该限制的有效方法。在这项研究中,我们证明了在高度丰富和复杂的菌群背景下,PMA定量聚合酶链反应(qPCR)用于检测指示生物(大肠杆菌和铜绿假单胞菌)的性能。用10μMPMA处理可导致死细胞DNA扩增产生的假阳性信号完全或显着减少。

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