Cevallos William, Fernández-Soto Pedro, Calvopiña Manuel, Fontecha-Cuenca Cristina, Sugiyama Hiromu, Sato Megumi, 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 Negl Trop Dis. 2017 Jun 19;11(6):e0005672. doi: 10.1371/journal.pntd.0005672. eCollection 2017 Jun.
Amphimeriasis is a fish-borne disease caused by the liver fluke Amphimerus spp. that has recently been reported as endemic in the tropical Pacific side of Ecuador with a high prevalence in humans and domestic animals. The diagnosis is based on the stool examination to identify parasite eggs, but it lacks sensitivity. Additionally, the morphology of the eggs may be confounded with other liver and intestinal flukes. No immunological or molecular methods have been developed to date. New diagnostic techniques for specific and sensitive detection of Amphimerus spp. DNA in clinical samples are needed.
METHODOLOGY/PRINCIPAL FINDINGS: A LAMP targeting a sequence of the Amphimerus sp. internal transcribed spacer 2 region was designed. Amphimerus sp. DNA was obtained from adult worms recovered from animals and used to optimize the molecular assays. Conventional PCR was performed using outer primers F3-B3 to verify the proper amplification of the Amphimerus sp. DNA target sequence. LAMP was optimized using different reaction mixtures and temperatures, and it was finally set up as LAMPhimerus. The specificity and sensitivity of both PCR and LAMP were evaluated. The detection limit was 1 pg of genomic DNA. Field testing was done using 44 human stool samples collected from localities where fluke is endemic. Twenty-five samples were microscopy positive for Amphimerus sp. eggs detection. In molecular testing, PCR F3-B3 was ineffective when DNA from fecal samples was used. When testing all human stool samples included in our study, the diagnostic parameters for the sensitivity and specificity were calculated for our LAMPhimerus assay, which were 76.67% and 80.77%, respectively.
CONCLUSIONS/SIGNIFICANCE: We have developed and evaluated, for the first time, a specific and sensitive LAMP assay for detecting Amphimerus sp. in human stool samples. The procedure has been named LAMPhimerus method and has the potential to be adapted for field diagnosis and disease surveillance in amphimeriasis-endemic areas. Future large-scale studies will assess the applicability of this novel LAMP assay.
双盘吸虫病是一种由双盘吸虫属肝吸虫引起的食源性疾病,最近有报道称其在厄瓜多尔热带太平洋沿岸地区为地方病,在人类和家畜中具有很高的患病率。诊断基于粪便检查以识别寄生虫卵,但缺乏敏感性。此外,虫卵的形态可能与其他肝吸虫和肠吸虫混淆。迄今为止,尚未开发出免疫或分子检测方法。因此,需要新的诊断技术来特异性和灵敏地检测临床样本中的双盘吸虫属DNA。
方法/主要发现:设计了一种针对双盘吸虫属内转录间隔区2序列的环介导等温扩增(LAMP)方法。从动物体内回收的成虫中获取双盘吸虫属DNA,并用于优化分子检测方法。使用外部引物F3-B3进行常规PCR,以验证双盘吸虫属DNA靶序列的正确扩增。使用不同的反应混合物和温度对LAMP进行优化,最终将其设置为LAMPhimerus。评估了PCR和LAMP的特异性和敏感性。检测限为1 pg基因组DNA。使用从吸虫流行地区收集的44份人类粪便样本进行现场测试。25份样本通过显微镜检查双盘吸虫属虫卵呈阳性。在分子检测中,当使用粪便样本的DNA时,PCR F3-B3无效。在检测我们研究中纳入的所有人类粪便样本时,计算了我们的LAMPhimerus检测方法的敏感性和特异性诊断参数,分别为76.67%和80.77%。
结论/意义:我们首次开发并评估了一种用于检测人类粪便样本中双盘吸虫属的特异性和灵敏的LAMP检测方法。该方法已被命名为LAMPhimerus方法,具有在双盘吸虫病流行地区适用于现场诊断和疾病监测的潜力。未来的大规模研究将评估这种新型LAMP检测方法的适用性。