Department of Genetics, Microbiology and Statistics, Microbiology Section, Faculty of Biology, University of Barcelona, Diagonal 643, E-08028, Barcelona, Spain.
Department of Genetics, Microbiology and Statistics, Microbiology Section, Faculty of Biology, University of Barcelona, Diagonal 643, E-08028, Barcelona, Spain.
Water Res. 2018 Jan 1;128:10-19. doi: 10.1016/j.watres.2017.10.030. Epub 2017 Oct 16.
The use of somatic coliphages as indicators of fecal and viral pollution in water and food has great potential due to the reliability, reproducibility, speed and cost effectiveness of methods for their detection. Indeed, several countries already use this approach in their water management policies. Although standardized protocols for somatic coliphage detection are available, user-friendly commercial kits would facilitate their routine implementation in laboratories. The new method presented here allows detection of up to 1 somatic coliphage in under 3.5 h, well within one working day. The method is based on a modified Escherichia coli strain with knocked-out uidB and uidC genes, which encode the transport of glucuronic acid inside cells, and overexpressing uidA, which encodes the enzyme β-glucuronidase. The enzyme accumulated in the bacterial cells only has contact with its substrate after cell lysis, such as that caused by phages, since the strain cannot internalize the substrate. When the enzyme is released into the medium, which contains a chromogen analogous to glucuronic acid, it produces a change of color from yellow to dark blue. This microbiological method for the determination of fecal pollution via the detection of culturable microorganisms can be applied to diverse sample types and volumes for qualitative (presence/absence) and quantitative analysis and is the fastest reported to date.
由于检测方法具有可靠性、可重复性、快速性和成本效益性,因此将体噬菌体用作水和食物中粪便和病毒污染的指示物具有很大的潜力。事实上,一些国家已经在其水资源管理政策中采用了这种方法。尽管已经有用于检测体噬菌体的标准化方案,但用户友好型商业试剂盒将有助于在实验室中常规实施。本研究提出的新方法可在 3.5 小时内检测到多达 1 个体噬菌体,完全在一个工作日内完成。该方法基于一个缺失 uidB 和 uidC 基因的改良大肠杆菌菌株,这些基因编码细胞内葡萄糖醛酸的转运,同时过度表达 uidA,该基因编码β-葡萄糖醛酸酶。只有在细胞裂解后,如噬菌体引起的细胞裂解,才会使积累在细菌细胞中的酶与底物接触,因为该菌株不能内化底物。当酶释放到含有类似于葡萄糖醛酸的显色底物的培养基中时,会产生从黄色到深蓝色的颜色变化。这种通过检测可培养微生物来确定粪便污染的微生物方法可应用于不同类型和体积的样本进行定性(存在/不存在)和定量分析,是迄今为止报道的最快方法。