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Rapid, convenient and efficient kit-independent detection of SARS-CoV-2 RNA.
Michel, Detlef; Danzer, Karin M; Groß, Rüdiger; Conzelmann, Carina; Müller, Janis A; Freischmidt, Axel; Weishaupt, Jochen H; Heller, Sandra; Münch, Jan; Michel, Manuela; Stamminger, Thomas; Kleger, Alexander; Otto, Markus.
  • Michel D; Institute for Virology, University Hospital Ulm, Ulm, Germany.
  • Danzer KM; Department of Neurology, Ulm University, Ulm, Germany. Electronic address: karin.danzer@uni-ulm.de.
  • Groß R; Institute of Molecular Virology, Ulm University Medical Centre, Ulm, Germany.
  • Conzelmann C; Institute of Molecular Virology, Ulm University Medical Centre, Ulm, Germany.
  • Müller JA; Institute of Molecular Virology, Ulm University Medical Centre, Ulm, Germany.
  • Freischmidt A; Department of Neurology, Ulm University, Ulm, Germany.
  • Weishaupt JH; Department of Neurology, Ulm University, Ulm, Germany.
  • Heller S; Department of Internal Medicine I, University Hospital Ulm, Ulm, Germany.
  • Münch J; Institute of Molecular Virology, Ulm University Medical Centre, Ulm, Germany.
  • Michel M; Institute for Virology, University Hospital Ulm, Ulm, Germany.
  • Stamminger T; Institute for Virology, University Hospital Ulm, Ulm, Germany.
  • Kleger A; Department of Internal Medicine I, University Hospital Ulm, Ulm, Germany. Electronic address: alexander.kleger@uni-ulm.de.
  • Otto M; Department of Neurology, Ulm University, Ulm, Germany.
J Virol Methods ; 286: 113965, 2020 12.
Article in English | MEDLINE | ID: covidwho-741388
ABSTRACT
Pandemic SARS-CoV-2 infection has rapidly developed into a socioeconomic and humanitarian catastrophe. Basic principles to prevent SARS-CoV-2 transmission are social distancing, face masks, contact tracing and early detection of SARS-CoV-2. To meet these requirements, virtually unlimited test capacities delivering results in a rapid and reliable manner are a prerequisite. Here, we provide and validate such a rapid, convenient and efficient kit-independent detection of SARS-CoV-2 RNA, termed COVID-quick-DET. This straightforward method operates with simple proteinase K treatment and repetitive heating steps with a sensitivity of 94.6% in head-to-head comparisons with kit-based isolation methods. This result is supported by data obtained from serially diluted SARS-CoV-2 virus stocks. Given its cost- and time-effective operation, COVID-quick-DET might be best suited for countries with general shortage or temporary acute scarcity of resources and equipment.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Reagent Kits, Diagnostic / RNA, Viral / Coronavirus Infections / Clinical Laboratory Techniques / Betacoronavirus Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: J Virol Methods Year: 2020 Document Type: Article Affiliation country: J.jviromet.2020.113965

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Reagent Kits, Diagnostic / RNA, Viral / Coronavirus Infections / Clinical Laboratory Techniques / Betacoronavirus Type of study: Diagnostic study / Prognostic study Limits: Humans Language: English Journal: J Virol Methods Year: 2020 Document Type: Article Affiliation country: J.jviromet.2020.113965