Author: Zhou, Lifeng; Chandrasekaran, Arun Richard; Punnoose, Jibin Abraham; Bonenfant, Gaston; Charles, Stephon; Levchenko, Oksana; Badu, Pheonah; Cavaliere, Cassandra; Pager, Cara T.; Halvorsen, Ken
                    Title: Programmable low-cost DNA-based platform for viral RNA detection  Cord-id: sjt4nkl1  Document date: 2020_9_25
                    ID: sjt4nkl1
                    
                    Snippet: Detection of viruses is critical for controlling disease spread. Recent emerging viral threats, including Zika virus, Ebola virus, and SARS-CoV-2 responsible for coronavirus disease 2019 (COVID-19) highlight the cost and difficulty in responding rapidly. To address these challenges, we develop a platform for low-cost and rapid detection of viral RNA with DNA nanoswitches that mechanically reconfigure in response to specific viruses. Using Zika virus as a model system, we show nonenzymatic detect
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: Detection of viruses is critical for controlling disease spread. Recent emerging viral threats, including Zika virus, Ebola virus, and SARS-CoV-2 responsible for coronavirus disease 2019 (COVID-19) highlight the cost and difficulty in responding rapidly. To address these challenges, we develop a platform for low-cost and rapid detection of viral RNA with DNA nanoswitches that mechanically reconfigure in response to specific viruses. Using Zika virus as a model system, we show nonenzymatic detection of viral RNA with selective and multiplexed detection between related viruses and viral strains. For clinical-level sensitivity in biological fluids, we paired the assay with sample preparation using either RNA extraction or isothermal preamplification. Our assay requires minimal laboratory infrastructure and is adaptable to other viruses, as demonstrated by quickly developing DNA nanoswitches to detect SARS-CoV-2 RNA in saliva. Further development and field implementation will improve our ability to detect emergent viral threats and ultimately limit their impact.
 
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