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评估VIDAS UP李斯特菌检测法(LPT)在多种食品和环境表面检测李斯特菌的性能:2013年10月首次行动。

Evaluation of VIDAS UP Listeria assay (LPT) for the detection of Listeria in a variety of foods and environmental surfaces: First Action 2013.10.

作者信息

Crowley Erin, Bird Patrick, Flannery Jonathan, Benzinger M Joseph, Fisher Kiel, Boyle Megan, Huffman Travis, Bastin Ben, Bedinghaus Paige, Judd William, Hoang Thao, Agin James, Goins David, Johnson Ronald L

出版信息

J AOAC Int. 2014 Mar-Apr;97(2):431-41. doi: 10.5740/jaoacint.13-372.

Abstract

The VIDAS UP Listeria (LPT) is an automated rapid screening enzyme phage-ligand based assay for the detection of Listeria species in human food products and environmental samples. The VIDAS LPT method was compared in a multi-laboratory collaborative study to AOAC Official Method 993.12 Listeria monocytogenes in Milk and Dairy Products reference method following current AOAC guidelines. A total of 14 laboratories participated, representing government and industry, throughout the United States. One matrix, queso fresco (soft Mexican cheese), was analyzed using two different test portion sizes, 25 and 125 g. Samples representing each test portion size were artificially contaminated with Listeria species at three levels, an uninoculated control level [0 colony-forming units (CFU)/test portion], a low-inoculum level (0.2-2 CFU/test portion), and a high-inoculum level (2-5 CFU/test portion). For this evaluation, 1800 unpaired replicate test portions were analyzed by either the VIDAS LPT or AOAC 993.12. Each inoculation level was analyzed using the Probability of Detection (POD) statistical model. For the low-level inoculated test portions, difference in collaborator POD (dLPOD) values of 0.01, (-0.10, 0.13), with 95% confidence intervals, were obtained for both 25 and 125 g test portions. The range of the confidence intervals for dLPOD values for both the 25 and 125 g test portions contains the point 0.0 indicating no statistically significant difference in the number of positive samples detected between the VIDAS LPT and the AOAC methods. In addition to Oxford agar, VIDAS LPT test portions were confirmed using Agar Listeria Ottavani and Agosti (ALOA), a proprietary chromogenic agar for the identification and differentiation of L. monocytogenes and Listeria species. No differences were observed between the two selective agars. The VIDAS LPT method, with the optional ALOA agar confirmation method, was adopted as Official First Action status for the detection of Listeria species in a variety of foods and environmental samples.

摘要

VIDAS UP李斯特菌检测试剂盒(LPT)是一种基于酶噬菌体配体的自动化快速筛查检测方法,用于检测人类食品和环境样本中的李斯特菌属。在一项多实验室合作研究中,按照美国官方分析化学师协会(AOAC)的现行指南,将VIDAS LPT方法与AOAC官方方法993.12(乳制品中单核细胞增生李斯特菌的检测方法)进行了比较。共有14个代表政府和行业的实验室参与了此次研究,实验室分布于美国各地。使用两种不同的测试份样量(25克和125克)对一种基质——墨西哥软奶酪(queso fresco)进行了分析。代表每种测试份样量的样本分别用三种不同水平的李斯特菌属进行人工污染,即未接种的对照水平[0个菌落形成单位(CFU)/测试份样]、低接种量水平(0.2 - 2 CFU/测试份样)和高接种量水平(2 - 5 CFU/测试份样)。在此次评估中,通过VIDAS LPT或AOAC 993.12方法对1800个非配对重复测试份样进行了分析。使用检测概率(POD)统计模型对每个接种水平进行分析。对于低接种量的测试份样,25克和125克测试份样的协作实验室POD(dLPOD)值差异均为0.01,95%置信区间为(-0.10, 0.13)。25克和125克测试份样的dLPOD值置信区间范围均包含0.0这一点,表明VIDAS LPT和AOAC方法检测到的阳性样本数量在统计学上无显著差异。除了牛津琼脂外,还使用了奥塔瓦尼和阿戈斯蒂李斯特菌琼脂(ALOA,一种用于鉴定和区分单核细胞增生李斯特菌和李斯特菌属的专利显色琼脂)对VIDAS LPT测试份样进行确认。两种选择性琼脂之间未观察到差异。VIDAS LPT方法以及可选的ALOA琼脂确认方法被采纳为检测各类食品和环境样本中李斯特菌属的官方首次行动方法。

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