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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:12
|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.
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页码:144 / 157
页数:14
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