Hybrid paper/PDMS microfluidic device integrated with RNA extraction and recombinase polymerase amplification for detection of norovirus in foods.

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Applied and Environmental Microbiology Pub Date : 2024-11-20 Epub Date: 2024-10-08 DOI:10.1128/aem.01208-24
Yuxiao Lu, Marti Z Hua, Yuhang Luo, Xiaonan Lu, Qian Liu
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引用次数: 0

Abstract

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 via 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.

Importance: 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.

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集成了 RNA 提取和重组聚合酶扩增技术的纸/PDMS 混合微流控装置,用于检测食品中的诺如病毒。
人类诺如病毒(HuNoV)被认为是食源性流行性胃肠炎爆发的主要致病因子。因此,人们对开发针对 HuNoV 的护理点检测提出了很高的要求。我们开发了一种折纸微流控装置,可快速检测小鼠诺瓦克病毒 1(MNV-1)(HuNoV 的替代病毒),包括从样品制备到结果可视化的整个过程。该过程包括通过纸带吸收 RNA、使用重组聚合酶扩增(RPA)进行 RNA 扩增以及用于信号读取的横向流动检测。芯片上的 MNV-1 检测在 35 分钟内完成,表明在我们的环境中对 MNV-1 具有 100% 的特异性。这种微流控装置对 MNV-1 的检测限为 200 PFU/mL,与管内 RPA 反应相当。它还成功检测了莴苣和树莓中的 MNV-1,浓度分别为 170 PFU/g 和 230 PFU/g,无需额外的浓缩步骤。该装置与等温核酸扩增技术具有很高的兼容性,在偏远地区和资源有限的环境中检测农业食品中的食源性病毒具有很大的潜力:HuNoV 属于 Caliciviridae 科,是可通过受污染食品传播的急性肠胃炎的主要病因。在导致腹泻和呕吐的急性肠胃炎病例中,每五例中就有一例是由 HuNoV 引起的,这给全球医疗保健系统带来了沉重负担。当食物在源头(如野生贻贝暴露于污染水域)、农场(如作物栽培、收获或牲畜处理过程中)、包装过程或餐饮活动中受到污染时,都可能爆发 HuNoV 疫情。这项研究成果拓展了 HuNoV 检测方法,为食品常规检测框架增添了价值。这种微流控装置可促进对 HuNoV 爆发的监测,减少农业食品行业的经济损失,提高食品安全。
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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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