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Rapid, Low-Cost Detection of Zika Virus Using Programmable Biomolecular Components
Author(s) -
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
Publication year - 2016
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2016.04.059
Subject(s) - zika virus , biology , crispr , computational biology , dengue virus , virology , flavivirus , guide rna , ebola virus , dengue fever , nasba , virus , cas9 , rna , genetics , gene
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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