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首页> 外文期刊>Applied and Environmental Microbiology >Rapid Detection and Enumeration of Giardia lamblia Cysts in Water Samples by Immunomagnetic Separation and Flow Cytometric Analysis
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Rapid Detection and Enumeration of Giardia lamblia Cysts in Water Samples by Immunomagnetic Separation and Flow Cytometric Analysis

机译:免疫磁分离和流式细胞术快速检测和计数水中贾第鞭毛虫囊肿

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Giardia lamblia is an important waterborne pathogen and is among the most common intestinal parasites of humans worldwide. Its fecal-oral transmission leads to the presence of cysts of this pathogen in the environment, and so far, quantitative rapid screening methods are not available for various matrices, such as surface waters, wastewater, or food. Thus, it is necessary to establish methods that enable reliable rapid detection of a single cyst in 10 to 100 liters of drinking water. Conventional detection relies on cyst concentration, isolation, and confirmation by immunofluorescence microscopy (IFM), resulting in low recoveries and high detection limits. Many different immunomagnetic separation (IMS) procedures have been developed for separation and cyst purification, so far with variable but high losses of cysts. A method was developed that requires less than 100 min and consists of filtration, resuspension, IMS, and flow cytometric (FCM) detection. MACS MicroBeads were used for IMS, and a reliable flow cytometric detection approach was established employing 3 different parameters for discrimination from background signals, i.e., green and red fluorescence (resulting from the distinct pattern emitted by the fluorescein dye) and sideward scatter for size discrimination. With spiked samples, recoveries exceeding 90% were obtained, and false-positive results were never encountered for negative samples. Additionally, the method was applicable to naturally occurring cysts in wastewater and has the potential to be automated.
机译:贾第鞭毛虫是一种重要的水生病原体,是全世界人类最常见的肠道寄生虫之一。它的粪便传播导致环境中存在这种病原体的囊肿,到目前为止,还没有定量的快速筛选方法可用于各种基质,例如地表水,废水或食物。因此,有必要建立能够可靠地快速检测10到100升饮用水中的单个囊肿的方法。常规检测依赖于囊肿浓度,分离和免疫荧光显微镜(IFM)确认,导致回收率低和检测限高。迄今为止,已经开发出许多不同的免疫磁分离(IMS)程序用于分离和囊肿纯化,但囊肿的损失却很大,但变化很大。开发了一种方法,该方法所需的时间少于100分钟,包括过滤,重悬,IMS和流式细胞术(FCM)检测。将MACS MicroBeads用于IMS,并建立了一种可靠的流式细胞术检测方法,该方法使用3个不同的参数来区分背景信号,即绿色和红色荧光(由于荧光素染料发出的不同图案)和侧向散射以进行大小区分。对于加标样品,回收率超过90%,阴性样品从未遇到假阳性结果。另外,该方法适用于废水中天然存在的囊肿,并且具有自动化的潜力。

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