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:14
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 95 条
[61]   Structural basis for the spectral difference in luciferase bioluminescence [J].
Nakatsu, T ;
Ichiyama, S ;
Hiratake, J ;
Saldanha, A ;
Kobashi, N ;
Sakata, K ;
Kato, H .
NATURE, 2006, 440 (7082) :372-376
[62]   Establishment of a loop-mediated isothermal amplification (LAMP) assay for the detection of phytoplasma-associated cassava witches' broom disease [J].
Nam Tuan Vu ;
Pardo, Juan Manuel ;
Alvarez, Elizabeth ;
Ham Huy Le ;
Wyckhuys, Kris ;
Kim-Lien Nguyen ;
Dung Tien Le .
APPLIED BIOLOGICAL CHEMISTRY, 2016, 59 (02) :151-156
[63]   Reverse transcription loop-mediated isothermal amplification of DNA for detection of Potato virus Y [J].
Nie, XZ .
PLANT DISEASE, 2005, 89 (06) :605-610
[64]   The application of loop-mediated isothermal amplification (LAMP) in food testing for bacterial pathogens and fungal contaminants [J].
Niessen, Ludwig ;
Luo, Jie ;
Denschlag, Carla ;
Vogel, Rudi F. .
FOOD MICROBIOLOGY, 2013, 36 (02) :191-206
[65]   Rapid and Sensitive Detection of Mycobacterium ulcerans by Use of a Loop-Mediated Isothermal Amplification Test [J].
Njiru, Zablon K. ;
Yeboah-Manu, Dorothy ;
Stinear, Timothy P. ;
Fyfe, Janet A. M. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2012, 50 (05) :1737-1741
[66]   Loop-mediated isothermal amplification of DNA [J].
Notomi, Tsugunori ;
Okayama, Hiroto ;
Masubuchi, Harumi ;
Yonekawa, Toshihiro ;
Watanabe, Keiko ;
Amino, Nobuyuki ;
Hase, Tetsu .
NUCLEIC ACIDS RESEARCH, 2000, 28 (12)
[67]   Comparison of a TaqMan real-time polymerase chain reaction assay with a loop-mediated isothermal amplification assay for detection of Gallid herpesvirus 1 [J].
Ou, Shan-Chia ;
Giambrone, Joseph J. ;
Macklin, Kenneth S. .
JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2012, 24 (01) :138-141
[68]   Real-time reverse transcription loop-mediated isothermal amplification for rapid detection of West Nile virus [J].
Parida, M ;
Posadas, G ;
Inoue, S ;
Hasebe, F ;
Morita, K .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (01) :257-263
[69]  
Rzezutka A, 2006, INT J FOOD MICROBIOL, V108, P315, DOI [10.1016/j.jfoodmicro.2005.11.016, 10.1016/j.ijfoodmicro.2005.11.016]
[70]   Hepatitis A virus detection in food:: current and future prospects [J].
Sanchez, G. ;
Bosch, A. ;
Pinto, R. M. .
LETTERS IN APPLIED MICROBIOLOGY, 2007, 45 (01) :1-5