日本脑炎
清脆的
病毒学
生物
病毒
环介导等温扩增
核糖核酸
逆转录环介导等温扩增
肠道病毒71
肠道病毒
分子生物学
计算生物学
脑炎
基因
逆转录酶
遗传学
DNA
作者
Bingrong Xu,Ping Gong,Yi Zhang,Yuan Wang,Dagang Tao,Lanting Fu,Emmanuel Mulaya Khazalwa,Hailong Liu,Shuhong Zhao,Xuying Zhang,Shengsong Xie
出处
期刊:Virus Research
[Elsevier BV]
日期:2022-07-13
卷期号:319: 198869-198869
被引量:16
标识
DOI:10.1016/j.virusres.2022.198869
摘要
Early and rapid detection of Japanese encephalitis virus (JEV) is necessary for timely preventive and control measures. However, JEV RNA detection remains challenging due to the low level of viremia. In this study, a RApid VIsual CRISPR (RAVI-CRISPR) assay based on reverse transcription loop-mediated isothermal amplification (RT-LAMP) and CRISPR/Cas12a targeting was developed for easy detection of JEV in the field. We showed successful detection of 8.97 or more copies of the C gene sequence of JEV RNA within approximately 60 min. This assay also displayed no cross-reactivity with other porcine pathogens. We applied our one-tube RAVI-CRISPR assay to 18 brain tissue sample for JE diagnosis. The results from both fluorescence intensity measurements and directly naked-eye visualization were consistent with those from real-time PCR analysis. Taken together, our results showed that one-tube RAVI-CRISPR assay is robust, convenient, sensitive, specific, affordable, and potentially adaptable to on-site detection or surveillance of JEV in clinical and vector samples.
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