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Survival, biofilm formation, and growth potential of environmental and enteric escherichia coli strains in drinking water microcosms

机译:环境和肠道大肠杆菌菌株在饮用水微观世界中的存活,生物膜形成和生长潜力

摘要

E. coli is the most commonly used indicator for faecal contamination in a drinking water distribution system (WDS). The assumption is that E. coli are of enteric origin and cannot persist for long outside their host, therefore acting as indicators of recent contamination events. This study investigates the fate of E. coli in drinking water; specifically addressing survival, biofilm formation under shear stress, and regrowth in a series of laboratory-controlled experiments. We show the extended persistence of three E. coli strains (two enteric and one soil isolate) in sterile and non-sterile drinking water microcosms, at 8 and 17°C, with T90 values ranging from 17.4 ± 1.8 to 149 ± 67.7 days, using standard plate counts and a series of (RT)-Q-PCR assays targeting 16S rRNA, tuf, uidA, and rodA genes and transcripts. Furthermore, each strain was capable of attaching to a surface and replicating to form biofilm in the presence of nutrients under a range of shear stress values (0.6, 2.0, and 4.4 dyn cm-2; BioFlux, Fluxion); however, cell numbers did not increase when drinking water was flowed over (t-test; p > 0.05). Finally, E. coli regrowth within drinking water microcosms containing PE-100 pipe-wall material was not observed in the biofilm or water phase using a combination of culturing and Q-PCR methods for E. coli. The results of this work highlight that when E. coli enters drinking water it has the potential to survive and attach to surfaces but that regrowth within drinking water or biofilm is unlikely.
机译:大肠杆菌是饮用水分配系统(WDS)中粪便污染的最常用指示剂。假定大肠杆菌是肠源性的,不能在宿主之外长期存在,因此可作为近期污染事件的指标。这项研究调查了饮用水中大肠杆菌的命运。在一系列实验室控制的实验中专门针对生存,在剪切应力下生物膜的形成以及再生长等问题。我们显示了三种大肠杆菌菌株(两种肠溶菌和一种土壤分离物)在无菌和非无菌饮用水微观世界中在8和17°C下的持久性扩展,其T90值范围为17.4±1.8至149±67.7天,使用标准板计数和一系列针对16S rRNA,tuf,uidA和rodA基因和转录本的(RT)-Q-PCR分析。此外,每种菌株能够在一定的剪切应力值(0.6、2.0和4.4 dyn cm-2; BioFlux,Fluxion)和一定的剪切应力值的条件下,附着于表面并复制形成生物膜。然而,当饮用水流过时,细胞数量并没有增加(t-检验; p> 0.05)。最后,结合使用大肠杆菌的培养和Q-PCR方法,在生物膜或水相中未观察到含有PE-100管壁材料的饮用水微观世界中的大肠杆菌再生长。这项工作的结果突出表明,当大肠杆菌进入饮用水时,它有可能生存并附着在表面,但是在饮用水或生物膜内再生的可能性很小。

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