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结合直接活菌计数(DVC)和荧光原位杂交(FISH)技术对河流和废水中的活大肠杆菌进行计数。

Combining direct viable count (DVC) and fluorescent in situ hybridisation (FISH) to enumerate viable E. coil in rivers and wastewaters.

作者信息

Armisen T Garcia, Servais P

机构信息

Ecologie des Systèmes Aquatiques, Université Libre de Bruxelles, Campus de la Plaine, Boulevard du Triomphe, B-1050 Bruxelles, Belgium.

出版信息

Water Sci Technol. 2004;50(1):271-5.

Abstract

In this study, a combination of the direct viable count procedure (DVC) and the FISH method was used to monitor by epifluorescence microscopy the abundance of viable E. coli in river water and wastewater samples. The DVC procedure consisted of exposing bacterial cells to a resuscitation medium containing antibiotics preventing cellular division and, thus, inducing an elongation of the viable cells. The FISH was performed using the "Colinsitu" probe specific for E. coil 16S r-RNA. Accuracy and detection limit of the epifluorescence microscopic DVC-FISH procedure were investigated. The method was then applied to river-water and wastewater samples. A good correlation was found in a log-log plot between the abundance of E. coil enumerated by a classical culture-based method (MPN method) and the DVC-FISH procedure. However, the DVC-FISH procedure gave consistently higher numbers. The ratio between both enumerations (DVC-FISH/MPN), which also indicated the ratio between viable and culturable E. coli, ranged between 2 and >30. It increased with decreasing abundance of culturable E. coli.

摘要

在本研究中,采用直接活菌计数法(DVC)和荧光原位杂交(FISH)方法相结合,通过落射荧光显微镜监测河水和废水样品中活菌大肠杆菌的丰度。DVC程序包括将细菌细胞暴露于含有抗生素的复苏培养基中,抗生素可阻止细胞分裂,从而诱导活菌细胞伸长。使用针对大肠杆菌16S r - RNA的“Colinsitu”探针进行FISH。研究了落射荧光显微镜DVC - FISH程序的准确性和检测限。然后将该方法应用于河水和废水样品。在基于经典培养方法(MPN法)计数的大肠杆菌丰度与DVC - FISH程序之间的双对数图中发现了良好的相关性。然而,DVC - FISH程序给出的数量始终更高。两种计数方法(DVC - FISH/MPN)的比值也表明了活菌与可培养大肠杆菌的比值,范围在2至>30之间。它随着可培养大肠杆菌丰度的降低而增加。

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