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Simultaneous Colorimetric Detection of a Variety of Salmonella spp. in Food and Environmental Samples by Optical Biosensing Using Oligonucleotide-Gold Nanoparticles

机译:同时比色检测各种沙门氏菌。寡核苷酸-金纳米颗粒的光学生物传感技术在食品和环境样品中的应用

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摘要

Optical biosensors for rapid detection of significant foodborne pathogens are steadily gaining popularity due to its simplicity and sensitivity. While nanomaterials such as gold nanoparticles (AuNPs) are commonly used as signal amplifiers for optical biosensors, AuNPs can also be utilized as a robust biosensing platform. Many reported optical biosensors were designed for individual pathogen detection in a single assay and have high detection limit (DL). Salmonella spp. is one of the major causative agents of foodborne sickness, hospitalization and deaths. Unfortunately, there are around 2,000 serotypes of Salmonella worldwide, and rapid and simultaneous detection of multiple strains in a single assay is lacking. In this study, a comprehensive and highly sensitive simultaneous colorimetric detection of nineteen (19) environmental and outbreak Salmonella spp. strains was achieved by a novel optical biosensing platform using oligonucleotide-functionalized AuNPs. A pair of newly designed single stranded oligonucleotides (30-mer) was displayed onto the surface of AuNPs (13 nm) as detection probes to hybridize with a conserved genomic region (192-bases) of ttrRSBCA found on a broad range of Salmonella spp. strains. The sandwich hybridization (30 min, 55°C) resulted in a structural formation of highly stable oligonucleotide/AuNPs-DNA complexes which remained undisturbed even after subjecting to an increased salt concentration (2 M, final), thus allowing a direct discrimination via color change of target (red color) from non-target (purplish-blue color) reaction mixtures by direct observation using the naked eye. In food matrices (blueberries and chicken meat), nineteen different Salmonella spp. strains were concentrated using immunomagnetic separation and then simultaneously detected in a 96-well microplate by oligonucleotide-functionalized AuNPs after DNA preparation. Successful oligonucleotide/AuNPs-DNA hybridization was confirmed by gel electrophoresis while AuNPs aggregation in non-target and control reaction mixtures was verified by both spectrophotometric analysis and TEM images. Results showed that the optical AuNP biosensing platform can simultaneously screen nineteen (19) viable Salmonella spp. strains tested with 100% specificity and a superior detection limit of <10 CFU/mL or g for both pure culture and complex matrices setups. The highly sensitive colorimetric detection system can significantly improve the screening and detection of viable Salmonella spp. strains present in complex food and environmental matrices, therefore reducing the risks of contamination and incidence of foodborne diseases.
机译:由于其简单性和灵敏性,用于快速检测重大食源性病原体的光学生物传感器正在稳步普及。尽管诸如金纳米颗粒(AuNPs)之类的纳米材料通常用作光学生物传感器的信号放大器,但AuNPs也可以用作坚固的生物传感平台。许多报道的光学生物传感器被设计用于在单个测定中检测单个病原体,并且具有高检测限(DL)。沙门氏菌是食源性疾病,住院和死亡的主要诱因之一。不幸的是,世界范围内约有2,000种血清型沙门氏菌,并且缺乏在单一测定中同时快速检测多种菌株的能力。在这项研究中,对十九(19)个环境和暴发性沙门氏菌进行了全面且高度灵敏的同时比色检测。通过使用寡核苷酸官能化的AuNP的新型光学生物传感平台获得了菌株。一对新设计的单链寡核苷酸(30-mer)作为检测探针展示在AuNPs(13 nm)的表面上,以与在广泛的沙门氏菌属中发现的ttrRSBCA的保守基因组区域(192个碱基)杂交。株。三明治杂交(30分钟,55°C)形成了结构稳定的高度稳定的寡核苷酸/ AuNPs-DNA复合物,即使在盐浓度增加(最终2 M)后仍保持不受干扰,因此可以通过颜色直接区分通过使用肉眼直接观察,可以从非目标(紫色-蓝色)反应混合物中改变目标(红色)的目标。在食品基质(蓝莓和鸡肉)中,有十九种不同的沙门氏菌。使用免疫磁分离法浓缩菌株,然后在DNA制备后通过寡核苷酸官能化的AuNP在96孔微孔板中同时检测。通过凝胶电泳证实了成功的寡核苷酸/ AuNPs-DNA杂交,同时通过分光光度分析和TEM图像验证了非目标和对照反应混合物中的AuNPs聚集。结果表明,光学AuNP生物传感平台可以同时筛查十九(19)种可行的沙门氏菌。对于纯培养物和复杂基质设置,均以100%特异性和卓越的检测限<10 CFU / mL或g进行了测试。高度灵敏的比色检测系统可以显着改善活沙门氏菌的筛选和检测。复杂食品和环境基质中存在的细菌,因此降低了污染和食源性疾病发病率的风险。

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