诺如病毒
核酸
生物芯片
核糖核酸
DNA
化学
RNA提取
寡核苷酸
病毒学
杂交探针
DNA提取
检出限
色谱法
分子生物学
聚合酶链反应
生物
纳米技术
病毒
生物化学
材料科学
基因
作者
Wen Ying Cui,Hyun Jin Yoo,Yun Guang Li,Changyoon Baek,Junhong Min
标识
DOI:10.1016/j.bios.2021.113878
摘要
Norovirus is one of the most common causes of gastroenteritis, a disease characterized by diarrhea, vomiting, and stomach pain. A rapid on-site identification of the virus from fecal samples of patients is a prerequisite for accurate medical management. Here, we demonstrate a rapid nucleic acid-based detection platform as an on-site biosensing tool that can concentrate viruses from fecal samples. Moreover, it can perform RNA extraction and identification, and signal amplification using G-quadruplex and hemin containing DNA probes (G-DNA probes) and graphene oxide (GO)-coated microbeads. Briefly, murine noroviruses are lysed without chemicals on the surface of the GO microbeads. Subsequently, the target RNA is hybridized with G-DNA probes, and the resultant RNA/G-DNA probe complex is separated from unbound G-DNA probes using GO beads and is mixed with the detection buffer (ABTS/H2O2). Presence of murine noroviruses causes a colorimetric change of the buffer from colorless to green. Thus, we integrated all processes required to detect murine noroviruses in stool samples in a simple foldable microfluidic chip. Moreover, it can detect 101 pfu of the virus in 30 min in a fecal sample.
科研通智能强力驱动
Strongly Powered by AbleSci AI