Zimmermann Meret, Schuppler Markus, Julian Timothy R, Kang Seju
Department of Environmental Microbiology, Eawag, Swiss Federal Institute of Aquatic Science and Technology, Dübendorf, Switzerland.
Laboratory of Food Microbiology, Institute of Food, Nutrition and Health, Swiss Federal Institute of Technology Zürich, Zürich, Switzerland.
Appl Environ Microbiol. 2025 Sep 17;91(9):e0088025. doi: 10.1128/aem.00880-25. Epub 2025 Aug 11.
Diarrheagenic is responsible for a substantial portion of foodborne diseases globally. The use of standard diagnostic tools for the detection of diarrheagenic often hampers the establishment of robust surveillance when no expensive laboratory equipment, such as thermocyclers, is present. Loop-mediated isothermal amplification (LAMP) has shown potential to enable the resource-efficient detection of pathogens. In this study, LAMP assays with two detection modes, fluorescence-based molecular beacon (MB) and nucleic acid lateral flow (NALF), were developed for the detection of the diarrheagenic strains Shiga toxin-producing (STEC), enteropathogenic (EPEC), and enterohemorrhagic (EHEC). Duplex LAMP assays for the virulence genes and of STEC, EPEC, and EHEC were developed and validated against wastewater from an on-site containment as a model environmental medium for wastewater-based surveillance in non-sewered areas. The developed LAMP assays showed moderate specificity toward and , enabling crude differentiation among STEC, EPEC, and EHEC. We assessed the sensitivity of the LAMP assays and estimated a Limit of Detection (LoD) of 10-10 gene copies per reaction and found moderate quantitative capability for the MB-based method. The development of LAMP assays for the specific detection of STEC, EPEC, and EHEC with two distinct detection modes provides various options for their surveillance in settings without access to thermocyclers.IMPORTANCEFoodborne diarrheagenic poses a public health threat, while the variability in transmissible agents hampers outbreak investigation. The lack of lab equipment, such as thermocyclers, in some laboratory settings obstructs the establishment of robust diagnostic tools. This study addresses the need for reliable diagnostic tools for thermocycler-independent application. Validation against wastewater from an on-site containment demonstrates detection of the targets in an environmental matrix that could provide representative epidemiological insights.
致泻性[病原体名称]是全球食源性疾病的重要病因。在没有昂贵实验室设备(如热循环仪)的情况下,使用标准诊断工具检测致泻性[病原体名称]往往会阻碍建立强有力的监测体系。环介导等温扩增技术(LAMP)已显示出能高效检测病原体的潜力。在本研究中,开发了基于荧光分子信标(MB)和核酸侧向流动(NALF)两种检测模式的LAMP检测方法,用于检测产志贺毒素[病原体名称](STEC)、肠致病性[病原体名称](EPEC)和肠出血性[病原体名称](EHEC)等致泻性菌株。针对STEC、EPEC和EHEC的毒力基因[基因名称1]和[基因名称2]开发了双重LAMP检测方法,并以现场隔离设施的废水作为非下水道地区基于废水监测的环境基质模型进行了验证。所开发的LAMP检测方法对[相关基因名称1]和[相关基因名称2]显示出中等特异性,能够对STEC、EPEC和EHEC进行初步区分。我们评估了LAMP检测方法的灵敏度,估计每个反应的检测限(LoD)为10-10个基因拷贝,并发现基于MB的方法具有中等定量能力。开发具有两种不同检测模式的用于特异性检测STEC、EPEC和EHEC的LAMP检测方法,为在没有热循环仪的情况下对其进行监测提供了多种选择。重要性食源性致泻性[病原体名称]对公众健康构成威胁,而传播媒介的多样性阻碍了疫情调查。在一些实验室环境中,缺乏热循环仪等实验室设备阻碍了建立强有力的诊断工具。本研究满足了对无需热循环仪即可应用的可靠诊断工具的需求。针对现场隔离设施废水的验证表明,能够在环境基质中检测到目标物,这可为流行病学提供有代表性的见解。