Center for Global Health Tumbes, Universidad Peruana Cayetano Heredia, Lima, Peru.
Oregon Health & Science University - Portland State University School of Public Health, Portland, Oregon, USA.
J Clin Microbiol. 2023 Jul 20;61(7):e0028223. doi: 10.1128/jcm.00282-23. Epub 2023 Jun 27.
Coproantigen detection by enzyme-linked immunosorbent assay (coAg ELISA) is a vital tool for detecting and treating cases of Taenia solium taeniasis. However, the assay's procedures require costly materials and sophisticated equipment, which are typically inaccessible in rural settings where the disease is endemic. To overcome these barriers, we developed and evaluated a field-applicable coAg ELISA. The field coAg ELISA was developed and evaluated across four phases using known positive and negative stool samples collected from northern Peru. Phase I focused on field assay development, phase II on a small-scale performance evaluation, phase III on a large-scale evaluation, and phase IV on the use and reliability of a colorimetric scale card. All samples were processed using the field and standard assay procedures and compared using signal-to-noise ratios, correlation tests, performance characteristics, and agreement statistics where appropriate. The field coAg ELISA using reagents stored at -20°C and commercially available water and milk powder, and relying on spontaneous separation of the supernatant, had performance comparable to the standard assay. The field coAg ELISA was strongly correlated with the standard in both the small- and large-scale laboratory evaluation ( = 0.99 and = 0.98, respectively). Finally, the field assay had an almost perfect agreement between independent readers (kappa = 0.975) and between each reader and the spectrophotometer. The field coAg ELISA demonstrated performance comparable to the standard, providing a low-cost alternative to the standard assay for identifying cases of intestinal taeniasis in a low-resource setting.
酶联免疫吸附测定(coAg ELISA)检测粪便抗原是检测和治疗猪带绦虫病的重要工具。然而,该检测方法需要昂贵的材料和复杂的设备,而这些在疾病流行的农村地区通常无法获得。为了克服这些障碍,我们开发并评估了一种适用于现场的 coAg ELISA。该现场 coAg ELISA 经过四个阶段的开发和评估,使用已知来自秘鲁北部的阳性和阴性粪便样本。第 I 阶段侧重于现场检测的开发,第 II 阶段侧重于小规模性能评估,第 III 阶段侧重于大规模评估,第 IV 阶段侧重于比色刻度卡的使用和可靠性。所有样本均使用现场和标准检测程序进行处理,并使用信噪比、相关测试、性能特征和适当的一致性统计数据进行比较。使用储存在-20°C 的试剂、市售的水和奶粉以及依靠上清液自发分离的现场 coAg ELISA 具有与标准检测相当的性能。现场 coAg ELISA 在小范围和大范围实验室评估中与标准检测均具有很强的相关性(r = 0.99 和 r = 0.98)。最后,现场检测在独立读者之间(κ=0.975)和每个读者与分光光度计之间具有几乎完美的一致性。现场 coAg ELISA 表现与标准相当,为在资源有限的环境中识别肠道带绦虫病病例提供了一种低成本的替代标准检测方法。