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

被引:0
作者
Lu, Yuxiao [1 ,2 ]
Hua, Marti Z. [2 ]
Luo, Yuhang [1 ]
Lu, Xiaonan [2 ]
Liu, Qian [1 ,3 ]
机构
[1] McGill Univ, Inst Parasitol, Ste Anne De Bellevue, PQ, Canada
[2] McGill Univ, Dept Food Sci & Agr Chem, Ste Anne De Bellevue, PQ, Canada
[3] Jewish Gen Hosp, Lady Davis Inst, McGill Ctr Viral Dis, Montreal, PQ, Canada
关键词
microfluidic device; lab-on-a-chip; isothermal amplification; food safety; norovirus; MURINE NOROVIRUS; VIRUS; INACTIVATION;
D O I
10.1128/aem.01208-24
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.IMPORTANCEHuNoV 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. 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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页数:14
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共 40 条
  • [21] Detection of multiple noroviruses associated with an international gastroenteritis outbreak linked to oyster consumption
    Le Guyader, Francoise S.
    Bon, Fabienne
    DeMedici, Dario
    Parnaudeau, Sylvain
    Bertone, Alessandra
    Crudeli, Silvia
    Doyle, Aoife
    Zidane, Mohamed
    Suffredini, Elisabetta
    Kohli, Evelyne
    Maddalo, Francesco
    Monini, Marina
    Gallay, Anne
    Pommepuy, Monique
    Pothier, Pierre
    Ruggeri, Franco M.
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2006, 44 (11) : 3878 - 3882
  • [22] Validation of EN ISO method 15216-Part 1-Quantification of hepatitis A virus and norovirus in food matrices
    Lowther, J. A.
    Bosch, A.
    Butot, S.
    Ollivier, J.
    Maede, D.
    Rutjes, S. A.
    Hardouin, G.
    Lombard, B.
    in't Veld, P.
    Leclercq, A.
    [J]. INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2019, 288 : 82 - 90
  • [23] Recombinase polymerase amplification: Basics, applications and recent advances
    Magrina Lobato, Ivan
    O'Sullivan, Ciara K.
    [J]. TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2018, 98 : 19 - 35
  • [24] Rapid (30-second), equipment-free purification of nucleic acids using easy-to-make dipsticks
    Mason, Michael G.
    Botella, Jose R.
    [J]. NATURE PROTOCOLS, 2020, 15 (11) : 3663 - 3677
  • [25] Müller L, 2016, PLOS CURR-TREE LIFE
  • [26] DNA detection using recombination proteins
    Piepenburg, Olaf
    Williams, Colin H.
    Stemple, Derek L.
    Armes, Niall A.
    [J]. PLOS BIOLOGY, 2006, 4 (07) : 1115 - 1121
  • [27] Development of a rapid and visual detection method for Rickettsia rickettsii combining recombinase polymerase assay with lateral flow test
    Qi, Yong
    Shao, Yinxiu
    Rao, Jixian
    Shen, Wanpeng
    Yin, Qiong
    Li, Xiaoling
    Chen, Hongxia
    Li, Jiameng
    Zeng, Wenwen
    Zheng, Shulong
    Liu, Suyun
    Li, Yuexi
    [J]. PLOS ONE, 2018, 13 (11):
  • [28] Multiple norovirus outbreaks linked to imported frozen raspberries
    Sarvikivi, E.
    Roivainen, M.
    Maunula, L.
    Niskanen, T.
    Korhonen, T.
    Lappalainen, M.
    Kuusi, M.
    [J]. EPIDEMIOLOGY AND INFECTION, 2012, 140 (02) : 260 - 267
  • [29] Paper-based nucleic acid sample preparation for point-of-care diagnostics
    Soni, Shruti
    Toley, Bhushan J.
    [J]. SENSORS AND ACTUATORS B-CHEMICAL, 2022, 355
  • [30] Extraction of food-borne viruses from food samples: A review
    Stals, Ambroos
    Baert, Leen
    Van Coillie, Els
    Uyttendaele, Mieke
    [J]. INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2012, 153 (1-2) : 1 - 9