Cevallos William, Fernández-Soto Pedro, Calvopiña Manuel, Buendía-Sánchez María, López-Abán Julio, Vicente Belén, Muro Antonio
Centro de Biomedicina, Carrera de Medicina, Universidad Central del Ecuador, Quito, Ecuador.
Infectious and Tropical Diseases Research Group (e-INTRO), Biomedical Research Institute of Salamanca-Research Centre for Tropical Diseases at the University of Salamanca (IBSAL-CIETUS), Faculty of Pharmacy, University of Salamanca, Salamanca, Spain.
PLoS One. 2018 Feb 14;13(2):e0192637. doi: 10.1371/journal.pone.0192637. eCollection 2018.
Amphimeriasis, a fish-borne zoonotic disease caused by the liver fluke Amphimerus spp., has recently been reported as an emerging disease affecting an indigenous Ameridian group, the Chachi, living in Ecuador. The only method for diagnosing amphimeriasis was the microscopic detection of eggs from the parasite in patients' stool samples with very low sensitivity. Our group developed an ELISA technique for detection of anti-Amphimerus IgG in human sera and a molecular method based on LAMP technology (named LAMPhimerus) for specific and sensitive parasite DNA detection. The LAMPhimerus method showed to be much more sensitive than classical parasitological methods for amphimeriasis diagnosis using human stool samples for analysis. The objective of this work is to demonstrate the feasibility of using dried stool samples on filter paper as source of DNA in combination with the effectiveness of our previously designed LAMPhimerus assay for successfully Amphimerus sp. detection in clinical stool samples. A total of 102 untreated and undiluted stool samples collected from Chachi population were spread as thin layer onto common filter paper for easily transportation to our laboratory and stored at room temperature for one year until DNA extraction. When LAMPhimerus method was applied for Amphimerus sp. DNA detection, a higher number of positive results was detected (61/102; 59.80%) in comparison to parasitological methods (38/102; 37.25%), including 28/61 (45.90%) microscopy-confirmed Amphimerus sp. infections. The diagnostic parameters for the sensitivity and specificity werecalculated for our LAMPhimerus assay, which were 79.17% and 65.98%, respectively. We demonstrate, for the first time, that common filter paper is useful for easy collection and long-term storage of human stool samples for later DNA extraction and molecular analysis of human-parasitic trematode eggs. This simple, economic and easily handling method combined with the specific and sensible LAMPhimerus assay has the potential to beused as an effective molecular large-scale screening test for amphimeriasis-endemic areas.
双腔吸虫病是一种由双腔吸虫属肝吸虫引起的食源性人畜共患疾病,最近有报道称它是一种影响生活在厄瓜多尔的美洲原住民查奇族的新兴疾病。诊断双腔吸虫病的唯一方法是在患者粪便样本中通过显微镜检测寄生虫卵,但其灵敏度非常低。我们团队开发了一种用于检测人血清中抗双腔吸虫IgG的ELISA技术,以及一种基于环介导等温扩增技术(称为LAMPhimerus)的分子方法,用于特异性和灵敏地检测寄生虫DNA。与使用人类粪便样本进行分析的双腔吸虫病诊断的传统寄生虫学方法相比,LAMPhimerus方法显示出更高的灵敏度。这项工作的目的是证明将滤纸上的干燥粪便样本用作DNA来源的可行性,以及我们之前设计的LAMPhimerus检测方法在临床粪便样本中成功检测双腔吸虫属的有效性。从查奇族人群中收集的总共102份未经处理和未稀释的粪便样本被薄薄地摊涂在普通滤纸上,以便轻松运输到我们的实验室,并在室温下保存一年,直到进行DNA提取。当使用LAMPhimerus方法检测双腔吸虫属DNA时,与寄生虫学方法(38/102;37.25%)相比,检测到的阳性结果数量更多(61/102;59.80%),其中包括28/61(45.90%)经显微镜确认的双腔吸虫属感染。计算了我们的LAMPhimerus检测方法的灵敏度和特异性诊断参数,分别为79.17%和65.98%。我们首次证明,普通滤纸可用于方便地收集和长期保存人类粪便样本,以便后续进行DNA提取和对人体寄生吸虫卵进行分子分析。这种简单、经济且易于操作的方法与特异性和灵敏的LAMPhimerus检测方法相结合,有可能作为双腔吸虫病流行地区有效的分子大规模筛查试验。