Institute of Parasitology, McGill University, Sainte-Anne-de-Bellevue, Quebec, Canada.
Department of Food Science and Agricultural Chemistry, McGill University, Sainte-Anne-de-Bellevue, Quebec, Canada.
Appl Environ Microbiol. 2024 Nov 20;90(11):e0120824. doi: 10.1128/aem.01208-24. Epub 2024 Oct 8.
Human norovirus (HuNoV) is recognized as the leading causative agent of foodborne outbreaks of epidemic gastroenteritis. Consequently, there is a high demand for developing point-of-care testing for HuNoV. We developed an origami microfluidic device that facilitates rapid detection of murine norovirus 1 (MNV-1), a surrogate for HuNoV, encompassing the entire process from sample preparation to result visualization. This process includes RNA absorption a paper strip, RNA amplification using recombinase polymerase amplification (RPA), and a lateral flow assay for signal readout. The on-chip detection of MNV-1 was completed within 35 min, demonstrating 100% specificity to MNV-1 in our settings. The detection limit of this microfluidic device for MNV-1 was 200 PFU/mL, comparable to the in-tube RPA reaction. It also successfully detected MNV-1 in lettuce and raspberries at concentrations of 170 PFU/g and 230 PFU/g, respectively, without requiring extra concentration steps. This device demonstrates high compatibility with isothermal nucleic acid amplification and holds significant potential for detecting foodborne viruses in agri-food products in remote and resource-limited settings.
HuNoV belongs to the family of Caliciviridae and is a leading cause of acute gastroenteritis that can be transmitted through contaminated foods. HuNoV causes around one out of five cases of acute gastroenteritis that lead to diarrhea and vomiting, placing a substantial burden on the healthcare system worldwide. HuNoV outbreaks can occur when food is contaminated at the source (e.g., wild mussels exposed to polluted water), on farms (e.g., during crop cultivation, harvesting, or livestock handling), during packaging, or at catered events. The research outcomes of this study expand the approaches of HuNoV testing, adding value to the framework for routine testing of food products. This microfluidic device can facilitate the monitoring of HuNoV outbreaks, reduce the economic loss of the agri-food industry, and enhance food safety.
人类诺如病毒(HuNoV)是食源性暴发流行胃肠炎的主要病原体。因此,人们迫切需要开发用于 HuNoV 的即时检测方法。我们开发了一种折纸微流控装置,可促进对鼠诺如病毒 1(MNV-1)的快速检测,MNV-1 是 HuNoV 的替代物,涵盖了从样品制备到结果可视化的整个过程。该过程包括 RNA 吸收在纸条上,使用重组酶聚合扩增(RPA)进行 RNA 扩增,以及用于信号读取的侧向流动分析。在我们的设定中,MNV-1 的芯片内检测在 35 分钟内完成,对 MNV-1 具有 100%的特异性。该微流控装置对 MNV-1 的检测限为 200PFU/mL,与管内 RPA 反应相当。它还成功地在生菜和覆盆子中检测到浓度分别为 170PFU/g 和 230PFU/g 的 MNV-1,而无需额外的浓缩步骤。该装置与等温核酸扩增具有高度兼容性,并且在偏远和资源有限的环境中用于检测农产品中的食源性病原体具有很大的潜力。
HuNoV 属于杯状病毒科,是导致急性胃肠炎的主要原因之一,可通过受污染的食物传播。HuNoV 导致全球约五分之一的急性胃肠炎病例,导致腹泻和呕吐,给全球医疗保健系统带来了巨大负担。当食物在源头(例如,暴露于污染水中的野生贻贝)、农场(例如,在作物种植、收获或牲畜处理期间)、包装过程中或在餐饮活动中受到污染时,就会发生 HuNoV 暴发。本研究的研究结果扩展了 HuNoV 检测方法,为食品产品的常规检测框架增添了价值。这种微流控装置可以促进 HuNoV 暴发的监测,减少农业食品行业的经济损失,并增强食品安全。