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Culture-Independent Techniques for Rapid Detection of Bacteria Associated with Loss of Chloramine Residual in a Drinking Water System

机译:快速检测与饮用水系统中氯胺残留相关的细菌的文化独立技术

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摘要

Chloramination is often the disinfection regimen of choice for extended drinking water systems. However, this process is prone to instability due to the growth of nitrifying bacteria. This is the first study to use alternative approaches for rapid investigation of chloraminated drinking water system instability in which flow cytometric cell sorting of bacteria with intact membranes (membrane-intact fraction) (BacLight kit) or with active esterases (esterase-active fraction) (carboxyfluorescein diacetate) was combined with 16S rRNA gene-directed PCR and denaturing gradient gel electrophoresis (DGGE). No active bacteria were detected when water left the water treatment plant (WTP), but 12 km downstream the chloramine residual had diminished and the level of active bacteria in the bulk water had increased to more than 1 × 105 bacteria ml−1. The bacterial diversity in the system was represented by six major DGGE bands for the membrane-intact fraction and 10 major DGGE bands for the esterase-active fraction. PCR targeting of the 16S rRNA gene of chemolithotrophic ammonia-oxidizing bacteria (AOB) and subsequent DGGE and DNA sequence analysis revealed the presence of an active Nitrosospira-related species and Nitrosomonas cryotolerans in the system, but no AOB were detected in the associated WTP. The abundance of active AOB was then determined by quantitative real-time PCR (qPCR) targeting the amoA gene; 3.43 × 103 active AOB ml−1 were detected in the membrane-intact fraction, and 1.40 × 104 active AOB ml−1 were detected in the esterase-active fraction. These values were several orders of magnitude greater than the 2.5 AOB ml−1 detected using a routine liquid most-probable-number assay. Culture-independent techniques described here, in combination with existing chemical indicators, should allow the water industry to obtain more comprehensive data with which to make informed decisions regarding remedial action that may be required either prior to or during an instability event.
机译:氯化法通常是扩展饮用水系统选择的消毒方案。然而,由于硝化细菌的生长,该过程易于不稳定。这是首次使用替代方法快速研究氯代饮用水系统不稳定性的研究,其中流式细胞术对具有完整膜(膜完整部分)(BacLight试剂盒)或具有活性酯酶(酯酶活性部分)的细菌进行分选(羧基荧光素二乙酸酯)与16S rRNA基因导向PCR和变性梯度凝胶电泳(DGGE)结合使用。当水离开水处理厂(WTP)时,没有检测到活性细菌,但是下游12 km的氯胺残留减少了,散装水中的活性细菌水平已增加到超过1×10 5 细菌ml -1 。该系统中的细菌多样性由膜完整级分的6个主要DGGE条带和酯酶活性级分的10个主要DGGE条带表示。以化营养性氨氧化细菌(AOB)的16S rRNA基因为靶点的PCR以及随后的DGGE和DNA序列分析显示,系统中存在活跃的亚硝基螺菌相关菌种和耐低温亚硝化单胞菌,但在相关的WTP中未检测到AOB。然后,通过针对amoA基因的定量实时PCR(qPCR)确定活性AOB的丰度。在膜完整部分中检测到3.43×10 3 活性AOB ml -1 ,而1.40×10 4 活性AOB ml 在酯酶活性级分中检测到-1 。这些值比使用常规液体最大概率数测定法检测到的2.5 AOB ml -1 大几个数量级。此处描述的与文化无关的技术,与现有化学指标结合,应可使水行业获得更全面的数据,以便就不稳定事件发生之前或期间可能需要的补救措施做出明智的决定。

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