Singh A, Yu F P, McFeters G A
Department of Microbiology, Montana State University, Bozeman 59717.
Appl Environ Microbiol. 1990 Feb;56(2):389-94. doi: 10.1128/aem.56.2.389-394.1990.
A modified direct viable count method to detect living bacteria was used with image analysis for the rapid enumeration of chlorine-injured cells in an Escherichia coli culture. The method was also used for determining chlorine-induced injury in coliform isolates and enteric pathogenic bacteria. Cultures were incubated in phosphate-buffered saline, containing 0.3% Casamino Acids (Difco Laboratories, Detroit, Mich.), 0.03% yeast extract, and optimal concentrations of nalidixic acid. Samples were withdrawn before and after incubation and stained with acridine orange, and cell lengths and breadths were measured by computerized image analysis. After incubation, cells which exceeded the mean preincubation length (viable cells) were enumerated and the results were compared with those obtained by the plate count method. Injury in the chlorine-exposed cell population was determined from the difference in viable count obtained with a nonselective Casamino Acids-yeast extract-nalidixic acid medium and a selective Casamino Acids-yeast extract-nalidixic acid medium containing sodium deoxycholate or sodium lauryl sulfate. The levels of injury determined by the direct viable count technique by using image analysis were comparable to those determined by the plate count method. The results showed that image analysis, under optimal conditions, enumerated significantly higher numbers of stressed E. coli than the plate count method did and detected injury in various cultures in 4 to 6 h.
采用一种改良的直接活菌计数法检测活细菌,并结合图像分析技术对大肠杆菌培养物中受氯损伤的细胞进行快速计数。该方法还用于测定大肠菌群分离株和肠道病原菌中氯诱导的损伤。将培养物在含有0.3%酪蛋白氨基酸(底特律密歇根州迪福科实验室)、0.03%酵母提取物和最佳浓度萘啶酸的磷酸盐缓冲盐水中培养。在培养前后取出样品,用吖啶橙染色,并通过计算机图像分析测量细胞的长度和宽度。培养后,对超过培养前平均长度的细胞(活细胞)进行计数,并将结果与平板计数法获得的结果进行比较。根据在非选择性酪蛋白氨基酸-酵母提取物-萘啶酸培养基和含有脱氧胆酸钠或十二烷基硫酸钠的选择性酪蛋白氨基酸-酵母提取物-萘啶酸培养基中获得的活菌计数差异,确定氯暴露细胞群体中的损伤情况。通过图像分析的直接活菌计数技术确定的损伤水平与平板计数法确定的损伤水平相当。结果表明,在最佳条件下,图像分析计数的应激大肠杆菌数量明显高于平板计数法,并且在4至6小时内检测到各种培养物中的损伤。