利用实时生物发光法(BART)和逆转录环介导等温扩增(RT-LAMP)技术快速检测食品中甲型肝炎病毒

IF 4.1 2区 农林科学 Q2 ENVIRONMENTAL SCIENCES Food and Environmental Virology Pub Date : 2023-01-14 DOI:10.1007/s12560-022-09548-7
Ruiqin Wu, Baozhong Meng, Milena Corredig, Mansel W. Griffiths
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引用次数: 2

摘要

食源性甲型肝炎感染已被认为是全球公共卫生的主要威胁。甲型肝炎病毒(HAV)感染发病率的增加与全球食品贸易的增长有关。快速、灵敏地检测食品中的甲肝病毒对调查疫情至关重要。实时RT-PCR是目前应用最广泛的甲肝病毒检测方法。然而,该技术依赖于扩增子的荧光测定,需要复杂、高成本的仪器和训练有素的人员,限制了其在低资源环境中的使用。在本研究中,我们开发了一种强大、经济、简单的检测方法,即逆转录环介导的等温扩增(RT-LAMP)与基于生物发光的实时扩增测定(BART)相结合,用于检测不同食物基质中的甲肝病毒,包括葱、草莓、贻贝和牛奶。研究了一步RT-LAMP-BART和两步RT-LAMP-BART检测不同食物基质中甲肝病毒的效率,并与实时RT-PCR进行了比较。RT-LAMP-BART检测的灵敏度受Mg2+浓度和引物质量的显著影响(P < 0.05)。一步RT-LAMP-BART的最佳Mg2+浓度为2 mM,两步RT-LAMP-BART的最佳浓度为4 mM。与墨盒纯化的引物相比,hplc纯化的引物可显著提高RT-LAMP-BART检测的灵敏度(P < 0.05)。对于不同食物基质中甲肝病毒的检测,两步RT-LAMP-BART的检测效果与实时RT-PCR相当,优于一步RT-LAMP-BART。两步RT-LAMP-BART法对青葱、草莓、贻贝、牛奶中HAV的检出限分别为8.3 × 100 PFU/15 g、8.3 × 101 PFU/50 g、8.3 × 100 PFU/5 g、8.3 × 100 PFU/40 mL。RT-LAMP-BART是一种简便、灵敏、可靠的食源性HAV检测方法。
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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

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 × 100 PFU/15 g, 8.3 × 101 PFU/50 g, 8.3 × 100 PFU/5 g, and 8.3 × 100 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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来源期刊
Food and Environmental Virology
Food and Environmental Virology ENVIRONMENTAL SCIENCES-MICROBIOLOGY
CiteScore
6.50
自引率
2.90%
发文量
35
审稿时长
1 months
期刊介绍: Food and Environmental Virology publishes original articles, notes and review articles on any aspect relating to the transmission of pathogenic viruses via the environment (water, air, soil etc.) and foods. This includes epidemiological studies, identification of novel or emerging pathogens, methods of analysis or characterisation, studies on survival and elimination, and development of procedural controls for industrial processes, e.g. HACCP plans. The journal will cover all aspects of this important area, and encompass studies on any human, animal, and plant pathogenic virus which is capable of transmission via the environment or food.
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