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一种用于对水中具有呼吸活性的肠出血性大肠杆菌O157:H7进行计数的快速、直接的方法。

A rapid, direct method for enumerating respiring enterohemorrhagic Escherichia coli O157:H7 in water.

作者信息

Pyle B H, Broadaway S C, McFeters G A

机构信息

Department of Microbiology, Montana State University, Bozeman 59717, USA.

出版信息

Appl Environ Microbiol. 1995 Jul;61(7):2614-9. doi: 10.1128/aem.61.7.2614-2619.1995.

Abstract

Simple, rapid methods for the detection and enumeration of specific bacteria in water and wastewater are needed. We have combined incubation using cyanoditolyl tetrazolium chloride (CTC) to detect respiratory activity with a modified fluorescent-antibody (FA) technique, for the enumeration of specific viable bacteria. Bacteria in suspensions were captured by filtration on nonfluorescent polycarbonate membranes that were then incubated on absorbent pads saturated with CTC medium. A specific antibody conjugated with fluorescein isothiocyanate was reacted with the cells on the membrane filter. The membrane filters were mounted for examination by epifluorescence microscopy with optical filters designed to permit concurrent visualization of fluorescent red-orange CTC-formazan crystals in respiring cells which were also stained with the specific FA. Experiments with Escherichia coli O157:H7 indicated that both respiratory activity and specific FA staining could be detected in logarithmic- or stationary-phase cultures, as well as in cells suspended in M9 medium or reverse-osmosis water. Following incubation without added nutrients in M9 medium or unsterile reverse-osmosis water, the E. coli O157:H7 populations increased, although lower proportions of the organisms reduced CTC. Numbers of CTC-positive, FA-positive cells compared with R2A agar plate counts gave a strong linear regression (R = 0.997). Differences in injury did not appear to affect CTC reduction. The procedure, which can be completed within 3 to 4 h, has also been performed successfully with Salmonella typhimurium and Klebsiella pneumoniae.

摘要

需要简单、快速的方法来检测和计数水和废水中的特定细菌。我们将使用氯化氰二苯四氮唑(CTC)检测呼吸活性的培养方法与改良的荧光抗体(FA)技术相结合,用于计数特定的活细菌。悬浮液中的细菌通过过滤捕获在非荧光聚碳酸酯膜上,然后将膜在饱和CTC培养基的吸水垫上孵育。与异硫氰酸荧光素偶联的特异性抗体与膜过滤器上的细胞反应。将膜过滤器安装好,通过落射荧光显微镜检查,使用设计用于同时观察呼吸细胞中荧光红橙色CTC-甲臜晶体的光学滤光片,这些细胞也用特异性FA染色。对大肠杆菌O157:H7的实验表明,在对数期或稳定期培养物中,以及悬浮在M9培养基或反渗透水中的细胞中,都可以检测到呼吸活性和特异性FA染色。在M9培养基或未灭菌的反渗透水中不添加营养物孵育后,大肠杆菌O157:H7的数量增加,尽管降低CTC的生物体比例较低。与R2A琼脂平板计数相比,CTC阳性、FA阳性细胞的数量给出了很强的线性回归(R = 0.997)。损伤差异似乎不影响CTC的降低。该程序可在3至4小时内完成,对鼠伤寒沙门氏菌和肺炎克雷伯菌也已成功进行。

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