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Assessing cross‐laboratory performance for quantifying coliphage using EPA Method 1642

机译:使用 EPA 方法 1642 评估定量大肠杆菌的跨实验室性能

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Abstract Aims Widespread adoption of the new U.S. Environmental Protection Agency (USEPA) Method 1642 for enumeration of coliphage in recreational water requires demonstration that laboratories consistently meet internal method performance goals and yield results that are consistent across laboratories. Methods and Results Here we assess the performance of six laboratories processing a series of blind wastewater‐ and coliphage‐spiked samples along with laboratory blanks. All laboratories met the method‐defined recovery requirements when performance was averaged across samples, with the few failures on individual samples mostly occurring for less‐experienced laboratories on the initial samples processed. Failures that occurred on later samples were generally attributed to easily correctable activities. Failure rates were higher for somatic vs. F+ coliphage, attributable to the more stringent performance criteria associated with somatic coliphage. There was no difference in failure rate between samples prepared in a marine water matrix compared to that in phosphate‐buffered saline. Conclusions Variation among laboratories was similar to that previously reported for enterococci, the current bacterial indicator used for evaluating beach water quality for public health protection. Significance and Impact of the Study These findings suggest that laboratory performance is not an inhibitor to the adoption of coliphage as a new indicator for assessing recreational health risk.
机译:摘要 目的 广泛采用新的美国环境保护署 (USEPA) 方法 1642 对娱乐用水中的大肠杆菌进行计数,需要证明实验室始终满足内部方法性能目标,并产生跨实验室一致的结果。方法和结果 在这里,我们评估了六个实验室处理一系列盲废水和大肠杆菌加标样品以及实验室空白样品的性能。当对样品的性能进行平均时,所有实验室都满足方法定义的回收率要求,单个样品的少数故障主要发生在经验不足的实验室处理的初始样品上。在后来的样品上发生的故障通常归因于易于纠正的活动。体细胞大肠杆菌的失败率高于F+大肠杆菌,这是由于与体细胞大肠杆菌相关的性能标准更严格。与磷酸盐缓冲盐水相比,在海水基质中制备的样品之间的失败率没有差异。结论 实验室之间的差异与之前报道的肠球菌相似,肠球菌是目前用于评估海滩水质以保护公共卫生的细菌指标。研究的意义和影响 这些发现表明,实验室表现并不阻碍采用大肠杆菌作为评估娱乐性健康风险的新指标。

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