检测点注意事项
寨卡病毒
环介导等温扩增
日本脑炎
计算生物学
病毒学
生物
脑炎
病毒
遗传学
免疫学
DNA
作者
Dong Ho You,Tong Xu,Bing-Zhou Huang,Ling Zhu,Fang Wu,Lishuang Deng,Zhe-Yan Liu,Jiaqi Duan,Yuan-Meng Wang,Liangpeng Ge,Zuohua Liu,Jing Sun,Xiu Zeng,Li-Qiao Lang,Yuancheng Zhou,Di-Shi Chen,Siyuan Lai,Yan-Ru Ai,Jianbo Huang,Zhiwen Xu
标识
DOI:10.1016/j.ijbiomac.2024.134151
摘要
Japanese encephalitis (JE), a mosquito-borne zoonotic disease caused by the Japanese encephalitis virus (JEV), poses a serious threat to global public health. The low viremia levels typical in JEV infections make RNA detection challenging, necessitating early and rapid diagnostic methods for effective control and prevention. This study introduces a novel one-pot detection method that combines recombinant enzyme polymerase isothermal amplification (RPA) with CRISPR/EsCas13d targeting, providing visual fluorescence and lateral flow assay (LFA) results. Our portable one-pot RPA-EsCas13d platform can detect as few as two copies of JEV nucleic acid within 1 h, without cross-reactivity with other pathogens. Validation against clinical samples showed 100 % concordance with real-time PCR results, underscoring the method's simplicity, sensitivity, and specificity. This efficacy confirms the platform's suitability as a novel point-of-care testing (POCT) solution for detecting and monitoring the JE virus in clinical and vector samples, especially valuable in remote and resource-limited settings.
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