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  1. Article ; Online: Programmable low-cost DNA-based platform for viral RNA detection.

    Zhou, Lifeng / Chandrasekaran, Arun Richard / Punnoose, Jibin Abraham / Bonenfant, Gaston / Charles, Stephon / Levchenko, Oksana / Badu, Pheonah / Cavaliere, Cassandra / Pager, Cara T / Halvorsen, Ken

    Science advances

    2020  Volume 6, Issue 39

    Abstract: ... for low-cost and rapid detection of viral RNA with DNA nanoswitches that mechanically reconfigure ... RNA with selective and multiplexed detection between related viruses and viral strains. For clinical ... adaptable to other viruses, as demonstrated by quickly developing DNA nanoswitches to detect SARS-CoV-2 RNA ...

    Abstract 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.
    MeSH term(s) Base Sequence ; Betacoronavirus/genetics ; COVID-19 ; Cell Line, Tumor ; Coronavirus Infections/diagnosis ; Coronavirus Infections/virology ; DNA, Single-Stranded/genetics ; Dengue/diagnosis ; Dengue/virology ; Dengue Virus/genetics ; Electrophoresis, Agar Gel/economics ; Electrophoresis, Agar Gel/methods ; Humans ; Limit of Detection ; Pandemics ; Pneumonia, Viral/diagnosis ; Pneumonia, Viral/virology ; RNA, Viral/genetics ; SARS-CoV-2 ; Saliva/virology ; Sequence Analysis, RNA/economics ; Sequence Analysis, RNA/methods ; Zika Virus/genetics ; Zika Virus Infection/diagnosis ; Zika Virus Infection/virology
    Chemical Substances DNA, Single-Stranded ; RNA, Viral
    Keywords covid19
    Language English
    Publishing date 2020-09-25
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2810933-8
    ISSN 2375-2548 ; 2375-2548
    ISSN (online) 2375-2548
    ISSN 2375-2548
    DOI 10.1126/sciadv.abc6246
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Programmable low-cost DNA-based platform for viral RNA detection

    Zhou, Lifeng / Chandrasekaran, Arun Richard / Punnoose, Jibin Abraham / Bonenfant, Gaston / Charles, Stephon / Levchenko, Oksana / Badu, Pheonah / Cavaliere, Cassandra / Pager, Cara T. / Halvorsen, Ken

    Science Advances

    2020  Volume 6, Issue 39, Page(s) eabc6246

    Abstract: ... for low-cost and rapid detection of viral RNA with DNA nanoswitches that mechanically reconfigure ... RNA with selective and multiplexed detection between related viruses and viral strains. For clinical ... adaptable to other viruses, as demonstrated by quickly developing DNA nanoswitches to detect SARS-CoV-2 RNA ...

    Abstract 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.
    Keywords covid19
    Language English
    Publisher American Association for the Advancement of Science (AAAS)
    Publishing country us
    Document type Article ; Online
    ZDB-ID 2810933-8
    ISSN 2375-2548
    ISSN 2375-2548
    DOI 10.1126/sciadv.abc6246
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Programmable low-cost DNA-based platform for viral RNA detection

    Zhou, Lifeng / Chandrasekaran, Arun Richard / Punnoose, Jibin Abraham / Bonenfant, Gaston / Charles, Stephon / Levchenko, Oksana / Badu, Pheonah / Cavaliere, Cassandra / Pager, Cara T. / Halvorsen, Ken

    bioRxiv

    Abstract: ... in responding rapidly. To address these challenges, we develop a platform for low-cost and rapid detection ... of viral RNA with DNA nanoswitches designed to mechanically reconfigure in response to specific viruses ... Using Zika virus as a model system, we show non-enzymatic detection of viral RNA to the attomole level ...

    Abstract Viral detection is critical for controlling disease spread and progression. Recent emerging viral threats including Zika, Ebola, and the current COVID-19 outbreak 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 designed to mechanically reconfigure in response to specific viruses. Using Zika virus as a model system, we show non-enzymatic detection of viral RNA to the attomole level, with selective and multiplexed detection between related viruses and viral strains. For clinical-level sensitivity in biological fluids, we paired the assay with a sample preparation step using either RNA extraction or isothermal pre-amplification. Our assay can be performed with minimal or no lab infrastructure, and is readily adaptable to detect other viruses. We demonstrate the adaptability of our method by quickly developing and testing DNA nanoswitches for detecting a fragment of SARS-CoV-2 RNA in human saliva. Given this versatility, we expect that further development and field implementation will improve our ability to detect emergent viral threats and ultimately limit their impact.
    Keywords covid19
    Publisher BioRxiv; MedRxiv
    Document type Article ; Online
    DOI 10.1101/2020.01.12.902452
    Database COVID19

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