Duan Lei, Yang Xiaohan, Zhan Wenli, Tang Yuan, Wei Mengru, Chen Keyi, Liu Pan, Xie Jia, Zhang Changbin, Zhao Hongyu, Luo Mingyong
Medical Genetic Centre, Guangdong Women and Children Hospital, Guangzhou, China.
Front Microbiol. 2022 Aug 24;13:912315. doi: 10.3389/fmicb.2022.912315. eCollection 2022.
Genogroup II genotype 4 (GII.4) norovirus causes acute gastroenteritis in children, and its infection is more severe than that of other genotypes. Early and precise detection and treatment are critical for controlling its spread and reducing the severity of infection. In this study, a rapid and efficient isothermal assay for the GII.4 norovirus detection (GII.4-CRISPR detection) was developed based on the CRISPR/Cas13a system. The assay can be applied without expensive instrumentation, and the results can be read both fluorescence and lateral flow strip (LFS). The analytical sensitivity of this assay was 5 copies/reaction, and there was no cross-reaction with other genotypes of norovirus or other clinically common pathogens. There was a coincidence rate of 100% between our assay and commercial quantitative polymerase chain reaction. GII.4-CRISPR detection improves upon the shortcomings of some previously established molecular methods of detection, particularly with regard to accessibility. It provides an alternative tool for outbreak control and early diagnosis of GII.4 norovirus infection.
基因Ⅱ群4型(GII.4)诺如病毒可导致儿童急性肠胃炎,且其感染比其他基因型更为严重。早期精准检测和治疗对于控制其传播及减轻感染严重程度至关重要。在本研究中,基于CRISPR/Cas13a系统开发了一种用于检测GII.4诺如病毒的快速高效等温检测方法(GII.4-CRISPR检测)。该检测方法无需昂贵仪器即可应用,结果可通过荧光和侧流条(LFS)读取。此检测方法的分析灵敏度为5拷贝/反应,与其他基因型诺如病毒或其他临床常见病原体无交叉反应。我们的检测方法与商业定量聚合酶链反应的符合率为100%。GII.4-CRISPR检测弥补了一些先前建立的分子检测方法的不足,尤其是在可及性方面。它为GII.4诺如病毒感染的疫情控制和早期诊断提供了一种替代工具。