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Identification of bacteria in drinking and purified water during the monitoring of a typical water purification system

机译:在监测典型净水系统期间,识别饮用水和纯净水中的细菌

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摘要

Abstract Background A typical purification system that provides purified water which meets ionic and organic chemical standards, must be protected from microbial proliferation to minimize cross-contamination for use in cleaning and preparations in pharmaceutical industries and in health environments. Methodology Samples of water were taken directly from the public distribution water tank at twelve different stages of a typical purification system were analyzed for the identification of isolated bacteria. Two miniature kits were used: (i) identification system (api 20 NE, Bio-Mérieux) for non-enteric and non-fermenting gram-negative rods; and (ii) identification system (BBL crystal, Becton and Dickson) for enteric and non-fermenting gram-negative rods. The efficiency of the chemical sanitizers used in the stages of the system, over the isolated and identified bacteria in the sampling water, was evaluated by the minimum inhibitory concentration (MIC) method. Results The 78 isolated colonies were identified as the following bacteria genera: Pseudomonas, Flavobacterium and Acinetobacter. According to the miniature kits used in the identification, there was a prevalence of isolation of P. aeruginosa 32.05%, P. picketti (Ralstonia picketti) 23.08%, P. vesiculares 12.82%, P. diminuta 11.54%, F. aureum 6.42%, P. fluorescens 5.13%, A. lwoffi 2.56%, P. putida 2.56%, P. alcaligenes 1.28%, P. paucimobilis 1.28%, and F. multivorum 1.28%. Conclusions We found that research was required for the identification of gram-negative non-fermenting bacteria, which were isolated from drinking water and water purification systems, since Pseudomonas genera represents opportunistic pathogens which disperse and adhere easily to surfaces, forming a biofilm which interferes with the cleaning and disinfection procedures in hospital and industrial environments.
机译:摘要背景必须提供一种典型的纯化系统,该系统所提供的纯净水必须满足离子和有机化学标准,因此必须防止其滋生微生物,以最大程度地减少交叉污染,以用于制药业和健康环境中的清洁和制剂。方法学在典型的净化系统的十二个不同阶段,直接从公共供水水箱中抽取水样进行分析,以鉴定分离出的细菌。使用了两种微型试剂盒:(i)鉴定系统(api 20 NE,Bio-Mérieux),用于非肠溶性和非发酵性革兰氏阴性菌; (ii)肠溶和非发酵革兰氏阴性棒的鉴定系统(BBL晶体,Becton和Dickson)。通过最小抑菌浓度(MIC)方法评估了系统各阶段使用的化学消毒剂对采样水中分离出的细菌的效率。结果分离出的78个菌落分别为假单胞菌,黄杆菌和不动杆菌。根据鉴定中使用的微型试剂盒,铜绿假单胞菌32.05%,p。picketti(Ralstonia picketti)23.08%,水泡P. vesiculares 12.82%,di.minminuta 11.54%,金黄色葡萄球菌6.42%的分离率很高。 ,萤光假单胞菌5.13%,l.offoffi假单胞菌2.56%,恶臭假单胞菌2.56%,产杯假单胞菌1.28%,古生体育假单胞菌1.28%和多齿拟杆菌1.28%。结论我们发现,鉴定从饮用水和净水系统中分离出来的革兰氏阴性非发酵菌是需要进行研究的,因为假单胞菌属代表机会病原体,它们容易分散并粘附在表面上,形成生物膜,从而干扰医院和工业环境中的清洁和消毒程序。

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