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Ultra-rapid detection of SARS-CoV-2 in public workspace environments
Ozlem Yaren; Jacquelyn McCarter; Nikhil Phadke; Kevin M Bradley; Benjamin Overton; Zunyi Yang; Shatakshi Ranade; Kunal Patil; Rishikesh Bangale; STEVEN A BENNER.
Affiliation
  • Ozlem Yaren; Foundation for Applied Molecular Evolution
  • Jacquelyn McCarter; Foundation for Applied Molecular Evolution
  • Nikhil Phadke; GenePath Diagnostics, Inc.
  • Kevin M Bradley; Foundation for Applied Molecular Evolution
  • Benjamin Overton; Firebird Biomolecular Sciences, LLC
  • Zunyi Yang; Firebird Biomolecular Sciences, LLC
  • Shatakshi Ranade; Genepath Diagnostics India Pvt. Ltd.
  • Kunal Patil; Genepath Diagnostics India Pvt. Ltd.
  • Rishikesh Bangale; Genepath Diagnostics India Pvt. Ltd.
  • STEVEN A BENNER; Foundation for Applied Molecular evolution
Preprint in English | medRxiv | ID: ppmedrxiv-20204131
Journal article
A scientific journal published article is available and is probably based on this preprint. It has been identified through a machine matching algorithm, human confirmation is still pending.
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ABSTRACT
Managing the pandemic caused by SARS-CoV-2 requires new capabilities in testing, including the possibility of identifying, in minutes, infected individuals as they enter spaces where they must congregate in a functioning society, including workspaces, schools, points of entry, and commercial business establishments. Here, the only useful tests (a) require no sample transport, (b) require minimal sample manipulation, (c) can be performed by unlicensed individuals, (d) return results on the spot in much less than one hour, and (e) cost no more than a few dollars. The sensitivity need not be as high as normally required by the FDA for screening asymptomatic carriers (as few as 10 virions per sample), as these viral loads are almost certainly not high enough for an individual to present a risk for forward infection. This allows tests specifically useful for this pandemic to trade-off unneeded sensitivity for necessary speed, simplicity, and frugality. In some studies, it was shown that viral load that creates forward-infection risk may exceed 105 virions per milliliter, easily within the sensitivity of an RNA amplification architecture, but unattainable by antibody-based architectures that simply target viral antigens. Here, we describe such a test based on a displaceable probe loop amplification architecture.
License
cc_by_nc_nd
Full text: Available Collection: Preprints Database: medRxiv Type of study: Diagnostic study / Prognostic study Language: English Year: 2020 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Diagnostic study / Prognostic study Language: English Year: 2020 Document type: Preprint
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