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Viral detection and identification in 20 min by rapid single-particle fluorescence in-situ hybridization of viral RNA.
Hepp, Christof; Shiaelis, Nicolas; Robb, Nicole C; Vaughan, Alison; Matthews, Philippa C; Stoesser, Nicole; Crook, Derrick; Kapanidis, Achillefs N.
  • Hepp C; Biological Physics Research Group, Clarendon Laboratory, Department of Physics, University of Oxford, Oxford, OX1 3PU, UK. christof.hepp@physics.ox.ac.uk.
  • Shiaelis N; Biological Physics Research Group, Clarendon Laboratory, Department of Physics, University of Oxford, Oxford, OX1 3PU, UK.
  • Robb NC; Biological Physics Research Group, Clarendon Laboratory, Department of Physics, University of Oxford, Oxford, OX1 3PU, UK.
  • Vaughan A; Warwick Medical School, University of Warwick, Coventry, CV4 7AL, UK.
  • Matthews PC; Nuffield Department for Medicine, University of Oxford, Oxford, OX3 9DU, UK.
  • Stoesser N; Nuffield Department for Medicine, University of Oxford, Oxford, OX3 9DU, UK.
  • Crook D; Nuffield Department for Medicine, University of Oxford, Oxford, OX3 9DU, UK.
  • Kapanidis AN; NIHR Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at the University of Oxford in Partnership With Public Health England, University of Oxford, Oxford, UK.
Sci Rep ; 11(1): 19579, 2021 10 01.
Article in English | MEDLINE | ID: covidwho-1447327
ABSTRACT
The increasing risk from viral outbreaks such as the ongoing COVID-19 pandemic exacerbates the need for rapid, affordable and sensitive methods for virus detection, identification and quantification; however, existing methods for detecting virus particles in biological samples usually depend on multistep protocols that take considerable time to yield a result. Here, we introduce a rapid fluorescence in situ hybridization (FISH) protocol capable of detecting influenza virus, avian infectious bronchitis virus and SARS-CoV-2 specifically and quantitatively in approximately 20 min, in virus cultures, combined nasal and throat swabs with added virus and likely patient samples without previous purification. This fast and facile workflow can be adapted both as a lab technique and a future diagnostic tool in enveloped viruses with an accessible genome.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viruses / RNA, Viral / In Situ Hybridization, Fluorescence Type of study: Diagnostic study / Prognostic study Language: English Journal: Sci Rep Year: 2021 Document Type: Article Affiliation country: S41598-021-98972-z

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viruses / RNA, Viral / In Situ Hybridization, Fluorescence Type of study: Diagnostic study / Prognostic study Language: English Journal: Sci Rep Year: 2021 Document Type: Article Affiliation country: S41598-021-98972-z