Augustine Swinburne A J, Eason Tarsha N, Simmons Kaneatra J, Curioso Clarissa L, Griffin Shannon M, Ramudit Malini K D, Plunkett Trevor R
National Exposure Research Laboratory, U.S. Environmental Protection Agency;
National Risk Management Research Laboratory, U.S. Environmental Protection Agency.
J Vis Exp. 2016 Sep 12(115):54415. doi: 10.3791/54415.
The etiology and impacts of human exposure to environmental pathogens are of major concern worldwide and, thus, the ability to assess exposure and infections using cost effective, high-throughput approaches would be indispensable. This manuscript describes the development and analysis of a bead-based multiplex immunoassay capable of measuring the presence of antibodies in human saliva to multiple pathogens simultaneously. Saliva is particularly attractive in this application because it is noninvasive, cheaper and easier to collect than serum. Antigens from environmental pathogens were coupled to carboxylated microspheres (beads) and used to measure antibodies in very small volumes of human saliva samples using a bead-based, solution-phase assay. Beads were coupled with antigens from Campylobacter jejuni, Helicobacter pylori, Toxoplasma gondii, noroviruses (G I.1 and G II.4) and hepatitis A virus. To ensure that the antigens were sufficiently coupled to the beads, coupling was confirmed using species-specific, animal-derived primary capture antibodies, followed by incubation with biotinylated anti-species secondary detection antibodies and streptavidin-R-phycoerythrin reporter (SAPE). As a control to measure non-specific binding, one bead set was treated identically to the others except it was not coupled to any antigen. The antigen-coupled and control beads were then incubated with prospectively-collected human saliva samples, measured on a high throughput analyzer based on the principles of flow cytometry, and the presence of antibodies to each antigen was measured in Median Fluorescence Intensity units (MFI). This multiplex immunoassay has a number of advantages, including more data with less sample; reduced costs and labor; and the ability to customize the assay to many targets of interest. Results indicate that the salivary multiplex immunoassay may be capable of identifying previous exposures and infections, which can be especially useful in surveillance studies involving large human populations.
人类暴露于环境病原体的病因及影响是全球主要关注的问题,因此,采用具有成本效益的高通量方法来评估暴露和感染的能力将不可或缺。本手稿描述了一种基于微珠的多重免疫测定法的开发与分析,该方法能够同时检测人唾液中针对多种病原体的抗体。在这种应用中,唾液特别具有吸引力,因为它是非侵入性的,比血清更便宜且更容易收集。将环境病原体的抗原偶联到羧化微球(珠子)上,并使用基于珠子的溶液相测定法在非常少量的人唾液样本中测量抗体。珠子与空肠弯曲菌、幽门螺杆菌、弓形虫、诺如病毒(G I.1和G II.4)以及甲型肝炎病毒的抗原偶联。为确保抗原充分偶联到珠子上,使用物种特异性的、动物源性的一级捕获抗体确认偶联,随后与生物素化的抗物种二级检测抗体和链霉亲和素 - R - 藻红蛋白报告分子(SAPE)孵育。作为测量非特异性结合的对照,一组珠子的处理方式与其他珠子相同,只是未偶联任何抗原。然后将抗原偶联的珠子和对照珠子与前瞻性收集的人唾液样本孵育,基于流式细胞术原理在高通量分析仪上进行测量,并以中位荧光强度单位(MFI)测量针对每种抗原的抗体的存在情况。这种多重免疫测定法具有许多优点,包括用更少的样本获得更多的数据;降低成本和劳动力;以及能够针对许多感兴趣的目标定制测定法。结果表明,唾液多重免疫测定法可能能够识别既往暴露和感染,这在涉及大量人群的监测研究中可能特别有用。