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Field-deployable viral diagnostics using CRISPR-Cas13
Journal article   Open access   Peer reviewed

Field-deployable viral diagnostics using CRISPR-Cas13

Cameron Myhrvold, Catherine A Freije, Jonathan S Gootenberg, Omar O Abudayyeh, Hayden C Metsky, Ann F Durbin, Max J Kellner, Amanda L Tan, Lauren M Paul, Leda A Parham, …
Science (American Association for the Advancement of Science), Vol.360(6387), pp.444-448
04-27-2018
PMCID: PMC6197056
PMID: 29700266

Abstract

Adaptation, Physiological - genetics Bacterial Proteins - chemistry CRISPR-Associated Proteins - chemistry Dengue - diagnosis Dengue Virus - genetics Dengue Virus - isolation & purification Endonucleases - chemistry Enzyme Assays Humans Microcephaly - diagnosis Microcephaly - virology Polymorphism, Single Nucleotide RNA, Viral - analysis Zika Virus - genetics Zika Virus - isolation & purification Zika Virus Infection - diagnosis
Mitigating global infectious disease requires diagnostic tools that are sensitive, specific, and rapidly field deployable. In this study, we demonstrate that the Cas13-based SHERLOCK (specific high-sensitivity enzymatic reporter unlocking) platform can detect Zika virus (ZIKV) and dengue virus (DENV) in patient samples at concentrations as low as 1 copy per microliter. We developed HUDSON (heating unextracted diagnostic samples to obliterate nucleases), a protocol that pairs with SHERLOCK for viral detection directly from bodily fluids, enabling instrument-free DENV detection directly from patient samples in <2 hours. We further demonstrate that SHERLOCK can distinguish the four DENV serotypes, as well as region-specific strains of ZIKV from the 2015-2016 pandemic. Finally, we report the rapid (<1 week) design and testing of instrument-free assays to detect clinically relevant viral single-nucleotide polymorphisms.
url
https://doi.org/10.1126/science.aas8836View
Published (Version of record) Open

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