Diyana Jamaluddin Nur, Ibrahim Nadiah, Yuziana Mohd Yusof Nurul, Ta Goh Choo, Ling Tan Ling
Southeast Asia Disaster Prevention Research Initiative (SEADPRI), Institute for Environment and Development (LESTARI), Universiti Kebangsaan Malaysia, 43600 UKM Bangi, Selangor Darul Ehsan, Malaysia.
Department of Earth Sciences and Environment, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 UKM Bangi, Selangor Darul Ehsan, Malaysia.
Opt Laser Technol. 2023 Jan;157:108763. doi: 10.1016/j.optlastec.2022.108763. Epub 2022 Oct 5.
The coronavirus disease (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged as a major public health outbreak in late 2019 and was proclaimed a global pandemic in March 2020. A reflectometric-based RNA biosensor was developed by using cysteamine-stabilized gold nanoparticles (cysAuNPs) as the colorimetric probe for bioassay of COVID-19 RNA (SARS-CoV-2 RNA) sequence. The cysAuNPs aggregated in the presence of DNA probes via cationic and anionic electrostatic attraction between the positively charged cysteamine ligands and the negatively charged sugar-phosphate backbone of DNA, whilst in the presence of target RNAs, the specific recognition between DNA probes and targets depleted the electrostatic interaction between the DNA probes and cysAuNPs signal probe, leading to dispersed particles. This has rendered a remarkable shifting in the surface plasmon resonance (SPR) on the basis of visual color change of the RNA biosensor from red to purplish hue at the wavelength of 765 nm. Optical evaluation of SARS-CoV-2 RNA by means on reflectance transduction of the RNA biosensor based on cysAuNPs optical sensing probes demonstrated rapid response time of 30 min with high sensitivity, good linearity and high reproducibility across a COVID-19 RNA concentration range of 25 nM to 200 nM, and limit of detection (LOD) at 0.12 nM. qPCR amplification of SARS-CoV-2 viral RNA showed good agreement with the proposed RNA biosensor by using spiked RNA samples of the oropharyngeal swab from COVID-19 patients. Therefore, this assay is useful for rapid and early diagnosis of COVID-19 disease including asymptomatic carriers with low viral load even in the presence of co-infection with other viruses that manifest similar respiratory symptoms.
由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的冠状病毒病(COVID-19)于2019年末成为重大公共卫生事件,并于2020年3月被宣布为全球大流行。通过使用半胱胺稳定的金纳米颗粒(cysAuNPs)作为比色探针,开发了一种基于反射测量的RNA生物传感器,用于对COVID-19 RNA(SARS-CoV-2 RNA)序列进行生物测定。在DNA探针存在的情况下,cysAuNPs通过带正电荷的半胱胺配体与带负电荷的DNA糖磷酸骨架之间的阳离子和阴离子静电吸引而聚集,而在靶RNA存在的情况下,DNA探针与靶之间的特异性识别耗尽了DNA探针与cysAuNPs信号探针之间的静电相互作用,导致颗粒分散。这使得RNA生物传感器在765nm波长处基于视觉颜色从红色变为紫色的变化,表面等离子体共振(SPR)发生了显著变化。基于cysAuNPs光学传感探针的RNA生物传感器的反射率转导对SARS-CoV-2 RNA进行光学评估,结果表明,在25 nM至200 nM的COVID-19 RNA浓度范围内,响应时间为30分钟,具有高灵敏度、良好的线性和高重现性,检测限(LOD)为0.12 nM。通过使用COVID-19患者口咽拭子的加标RNA样本,对SARS-CoV-2病毒RNA进行qPCR扩增,结果与所提出的RNA生物传感器显示出良好的一致性。因此,该检测方法可用于COVID-19疾病的快速早期诊断,包括病毒载量低的无症状携带者,即使存在与表现出类似呼吸道症状的其他病毒的合并感染。