Rapid Detection of Hepatitis A Virus in Foods Using a Bioluminescent Assay in Real-Time (BART) and Reverse Transcription Loop-Mediated Isothermal Amplification (RT-LAMP) Technology

被引:11
|
作者
Wu, Ruiqin [1 ,2 ]
Meng, Baozhong [3 ]
Corredig, Milena [1 ]
Griffiths, Mansel W. W. [1 ,2 ]
机构
[1] Univ Guelph, Dept Food Sci, 50 Stone Rd East, Guelph, ON N1G 2W1, Canada
[2] Canadian Res Inst Food Safety, 43 McGilvray St, Guelph, ON N1G 2W1, Canada
[3] Univ Guelph, Dept Mol & Cellular Biol, 50 Stone Rd East, Guelph, ON N1G 2W1, Canada
关键词
Hepatitis A virus; Detection; RT-LAMP-BART; Food; QUANTITATIVE DETECTION; COLORIMETRIC DETECTION; VISUAL DETECTION; ENTERIC VIRUSES; PCR; PATHOGENS; CHIP; GENE; DNA; IDENTIFICATION;
D O I
10.1007/s12560-022-09548-7
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Foodborne hepatitis A infections have been considered as a major threat for public health worldwide. Increased incidences of hepatitis A virus (HAV) infection has been associated with growing global trade of food products. Rapid and sensitive detection of HAV in foods is very essential for investigating the outbreaks. Real-time RT-PCR has been most widely used for the detection of HAV by far. However, the technology relies on fluorescence determination of the amplicon and requires sophisticated, high-cost instruments and trained personnel, limiting its use in low resource settings. In this study, a robust, affordable, and simple assay, reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay in combination with a bioluminescence-based determination of amplification in real-time (BART), was developed for the detection of HAV in different food matrices, including green onion, strawberry, mussel, and milk. The efficiencies of a one-step RT-LAMP-BART and a two-step RT-LAMP-BART were investigated for the detection of HAV in different food matrices and was compared with that of real-time RT-PCR. The sensitivity of the RT-LAMP-BART assay was significantly affected by Mg2+ concentration (P < 0.05), in addition to primer quality. The optimal Mg2+ concentration was 2 mM for one-step RT-LAMP-BART and 4 mM for two-step RT-LAMP-BART. Compared with cartridge-purified primers, HPLC-purified primers could greatly improve the sensitivity of the RT-LAMP-BART assay (P < 0.05). For detecting HAV in different food matrices, the performance of two-step RT-LAMP-BART was comparable with that of real-time RT-PCR and was better than that of one-step RT-LAMP-BART. The detection limit of the two-step RT-LAMP-BART for HAV in green onion, strawberry, mussel, and milk was 8.3 x 10(0) PFU/15 g, 8.3 x 10(1) PFU/50 g, 8.3 x 10(0) PFU/5 g, and 8.3 x 10(0) PFU/40 mL, respectively. The developed RT-LAMP-BART was an effective, simple, sensitive, and robust method for foodborne HAV detection.
引用
收藏
页码:144 / 157
页数:14
相关论文
共 50 条
  • [31] Rapid and efficient detection of mycoplasma pneumonia RNA by reverse-transcription loop-mediated isothermal amplification (RT-LAMP)
    Ma, Cuiping
    Yan, Chunyu
    Shi, Chao
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2018, 255
  • [32] Development and Application of Reverse Transcription Loop-mediated Isothermal Amplification (RT-LAMP) for Feline Coronavirus Detection
    Techangamsuwan, Somporn
    Radtanakatikanon, Araya
    Thanawongnuwech, Roongroje
    THAI JOURNAL OF VETERINARY MEDICINE, 2013, 43 (02): : 229 - 233
  • [33] One-step reverse transcription loop-mediated isothermal amplification (RT-LAMP) for detection of tomato torrado virus
    Marta Budziszewska
    Przemysław Wieczorek
    Aleksandra Obrępalska-Stęplowska
    Archives of Virology, 2016, 161 : 1359 - 1364
  • [34] Multiplex detection of three banana viruses by reverse transcription loop-mediated isothermal amplification (RT-LAMP)
    Zhang, Jingxin
    Borth, Wayne
    Lin, Birun
    Melzer, Michael
    Shen, Huifang
    Pu, Xiaoming
    Sun, Dayuan
    Nelson, Scot
    Hu, John
    TROPICAL PLANT PATHOLOGY, 2018, 43 (06): : 543 - 551
  • [35] One-step reverse transcription loop-mediated isothermal amplification (RT-LAMP) for detection of tomato torrado virus
    Budziszewska, Marta
    Wieczorek, Przemysaw
    Obrepalska-Steplowska, Aleksandra
    ARCHIVES OF VIROLOGY, 2016, 161 (05) : 1359 - 1364
  • [36] Multiplex detection of three banana viruses by reverse transcription loop-mediated isothermal amplification (RT-LAMP)
    Jingxin Zhang
    Wayne Borth
    Birun Lin
    Michael Melzer
    Huifang Shen
    Xiaoming Pu
    Dayuan Sun
    Scot Nelson
    John Hu
    Tropical Plant Pathology, 2018, 43 : 543 - 551
  • [37] Real-time reverse transcription loop-mediated isothermal amplification for rapid detection of West Nile virus
    Parida, M
    Posadas, G
    Inoue, S
    Hasebe, F
    Morita, K
    JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (01) : 257 - 263
  • [38] A Rapid and Sensitive Reverse Transcription-Loop-Mediated Isothermal Amplification (RT-LAMP) Assay for the Detection of Indian Citrus Ringspot Virus
    Kokane, Amol D.
    Kokane, Sunil B.
    Warghane, Ashish J.
    Gubyad, Mrugendra G.
    Sharma, Ashwani Kumar
    Reddy, M. Krishna
    Ghosh, Dilip Kumar
    PLANT DISEASE, 2021, 105 (05) : 1346 - 1355
  • [39] Rapid, simple detection of banana bract mosaic virus in abaca using a one-step reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay
    Rhosener Bhea L. Koh
    Cris Francis C. Barbosa
    Vermando M. Aquino
    Leny C. Galvez
    Journal of General Plant Pathology, 2020, 86 : 433 - 441
  • [40] Rapid, simple detection of banana bract mosaic virus in abaca using a one-step reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay
    Koh, Rhosener Bhea L.
    Barbosa, Cris Francis C.
    Aquino, Vermando M.
    Galvez, Leny C.
    JOURNAL OF GENERAL PLANT PATHOLOGY, 2020, 86 (06) : 433 - 441