寨卡病毒
生物
计算生物学
清脆的
登革热病毒
病毒学
引导RNA
埃博拉病毒
登革热
纳斯巴
Cas9
黄病毒
核糖核酸
病毒
遗传学
基因
作者
Keith Pardee,Alexander A. Green,Melissa K. Takahashi,Dana Braff,Guillaume Lambert,Jeong Wook Lee,Tom Ferrante,Duo Ma,Nina M. Donghia,Melina Fan,Nichole M. Daringer,Irene Bosch,Dawn M. Dudley,David H. O’Connor,Lee Gehrke,James J. Collins
出处
期刊:Cell
[Cell Press]
日期:2016-05-01
卷期号:165 (5): 1255-1266
被引量:1235
标识
DOI:10.1016/j.cell.2016.04.059
摘要
The recent Zika virus outbreak highlights the need for low-cost diagnostics that can be rapidly developed for distribution and use in pandemic regions. Here, we report a pipeline for the rapid design, assembly, and validation of cell-free, paper-based sensors for the detection of the Zika virus RNA genome. By linking isothermal RNA amplification to toehold switch RNA sensors, we detect clinically relevant concentrations of Zika virus sequences and demonstrate specificity against closely related Dengue virus sequences. When coupled with a novel CRISPR/Cas9-based module, our sensors can discriminate between viral strains with single-base resolution. We successfully demonstrate a simple, field-ready sample-processing workflow and detect Zika virus from the plasma of a viremic macaque. Our freeze-dried biomolecular platform resolves important practical limitations to the deployment of molecular diagnostics in the field and demonstrates how synthetic biology can be used to develop diagnostic tools for confronting global health crises. PAPERCLIP.
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