Facile and foldable point-of-care biochip for nucleic acid based-colorimetric detection of murine norovirus in fecal samples using G-quadruplex and graphene oxide coated microbeads

被引:17
作者
Cui, Wen Ying [1 ]
Yoo, Hyun Jin [1 ]
Li, Yun Guang [1 ]
Baek, Changyoon [1 ]
Min, Junhong [1 ]
机构
[1] Chung Ang Univ, Sch Integrat Engn, Seoul, South Korea
关键词
Murine norovirus; Fecal samples; Sample preparation; On-site biosensor; Graphene oxide-coated microbeads; Nucleic-acid based detection; MEDIATED ISOTHERMAL AMPLIFICATION; ASYMPTOMATIC FOOD HANDLERS; DNA; ADSORPTION; INFECTIONS; BINDING; PCR;
D O I
10.1016/j.bios.2021.113878
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
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 ac-curate 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 10(1) pfu of the virus in 30 min in a fecal sample.
引用
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页数:9
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