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基于环介导等温扩增技术的[病原体名称]毒力相关基因简易可视化检测方法 (注:原文中“of”后缺少具体病原体名称)

Simple Visualized Detection Method of Virulence-Associated Genes of by Loop-Mediated Isothermal Amplification.

作者信息

Xu Mengjie, Fu Huiyu, Chen Dailing, Shao Zehuai, Zhu Jun, Alali Walid Q, Chen Lanming

机构信息

Key Laboratory of Quality and Safety Risk Assessment for Aquatic Products on Storage and Preservation (Shanghai), China Ministry of Agriculture, College of Food Science and Technology, Shanghai Ocean University, Shanghai, China.

Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.

出版信息

Front Microbiol. 2019 Dec 20;10:2899. doi: 10.3389/fmicb.2019.02899. eCollection 2019.

Abstract

is a leading waterborne pathogenic bacterium worldwide. It can cause human cholera that is still pandemic in developing nations. Detection of . contamination in drinking water and aquatic products is imperative for assuring food safety. In this study, a simple, sensitive, specific, and visualized method was developed based on loop-mediated isothermal amplification (LAMP) (designated sssvLAMP) to detect virulence-associated (, , , , and ) and species-specific () genes of Three pairs of oligonucleotide primers (inner, outer, and loop primers) were designed and or synthesized to target each of these genes. The optimal conditions of the sssvLAMP method was determined, and one-step sssvLAMP reaction was performed at 65°C for 40 min. Positive results were simply read by the naked eye via color change (from orange to light green) under the visible light, or by the production of green fluorescence under the UV light (260 nm). The sssvLAMP method was more efficient in detecting 6.50 × 10-6.45 × 10-fold low number of cells, and more sensitive in genomic DNA (1.36 × 10-4.42 × 10 ng/reaction) than polymerase chain reaction (PCR) method. Among 52 strains of and 50 strains of non-target species (e.g., other and common pathogens) examined, the sensitivity and specificity of the sssvLAMP method were 100% for all the target genes. Similar high efficiency of the method was observed when tested with spiked samples of water and aquatic products, as well as human stool specimens. Water from various sources and commonly consumed fish samples were promptly screened by this simple and efficient visualized method and diversified variation in the occurrence of the target genes was observed. strains could be mostly detected by the presence of and alone or in combination with other genes, indicating a variable risk of potentially pathogenic non-O1/O139 strains in edible food products. This novel LAMP method can be a promising tool to address the increasing need of food safety control of aquatic products.

摘要

是全球主要的水源性致病细菌。它可引发人类霍乱,在发展中国家仍呈大流行态势。检测饮用水和水产品中的污染对于确保食品安全至关重要。在本研究中,基于环介导等温扩增技术(LAMP)开发了一种简单、灵敏、特异且可视化的方法(命名为sssvLAMP),用于检测霍乱弧菌的毒力相关基因(、、、、和)以及种特异性基因()。设计并合成了三对寡核苷酸引物(内引物、外引物和环引物),分别靶向这些基因。确定了sssvLAMP方法的最佳条件,一步法sssvLAMP反应在65°C下进行40分钟。阳性结果可通过肉眼在可见光下观察颜色变化(从橙色变为浅绿色)简单读取,或在紫外光(260 nm)下观察绿色荧光产生情况读取。sssvLAMP方法在检测低至6.50×10 - 6.45×10倍数量的霍乱弧菌细胞时更高效,并且在检测霍乱弧菌基因组DNA(1.36×10 - 4.42×10 ng/反应)方面比聚合酶链反应(PCR)方法更灵敏。在所检测的52株霍乱弧菌和50株非靶标物种(如其他弧菌和常见病原体)中,sssvLAMP方法对所有靶标基因的灵敏度和特异性均为100%。在用添加了霍乱弧菌的水和水产品以及人类粪便标本进行测试时,观察到该方法具有类似的高效性。通过这种简单高效的可视化方法对来自各种水源的水和常见食用鱼样本进行了快速筛查,并观察到靶标基因出现情况的多样化变化。霍乱弧菌菌株大多可通过单独存在或与其他基因组合存在的和进行检测,表明食用食品中潜在致病性非O1/O139菌株存在可变风险。这种新型LAMP方法可能成为满足日益增长的水产品食品安全控制需求的有前景的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0d8/6932958/71b242565dbb/fmicb-10-02899-g001.jpg

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