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Visualization of SARS-CoV-2 using Immuno RNA-Fluorescence In Situ Hybridization.
Kula-Pacurar, Anna; Wadas, Jakub; Suder, Agnieszka; Szczepanski, Artur; Milewska, Aleksandra; Ochman, Marek; Stacel, Tomasz; Pyrc, Krzysztof.
  • Kula-Pacurar A; Malopolska Centre of Biotechnology, Jagiellonian University; anna.kula-pacurar@uj.edu.pl.
  • Wadas J; Microbiology Department Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University.
  • Suder A; Malopolska Centre of Biotechnology, Jagiellonian University.
  • Szczepanski A; Malopolska Centre of Biotechnology, Jagiellonian University; Microbiology Department Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University.
  • Milewska A; Malopolska Centre of Biotechnology, Jagiellonian University; Microbiology Department Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University.
  • Ochman M; Department of Cardiac, Vascular and Endovascular Surgery and Transplantology, The Medical University of Silesia in Katowice; Silesian Centre for Heart Diseases.
  • Stacel T; Department of Cardiac, Vascular and Endovascular Surgery and Transplantology, The Medical University of Silesia in Katowice; Silesian Centre for Heart Diseases.
  • Pyrc K; Malopolska Centre of Biotechnology, Jagiellonian University; k.a.pyrc@uj.edu.pl.
J Vis Exp ; (166)2020 12 23.
Article in English | MEDLINE | ID: covidwho-1022040
ABSTRACT
This manuscript provides a protocol for in situ hybridization chain reaction (HCR) coupled with immunofluorescence to visualize severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA in cell line and three-dimensional (3D) cultures of human airway epithelium. The method allows highly specific and sensitive visualization of viral RNA by relying on HCR initiated by probe localization. Split-initiator probes help amplify the signal by fluorescently labeled amplifiers, resulting in negligible background fluorescence in confocal microscopy. Labeling amplifiers with different fluorescent dyes facilitates the simultaneous recognition of various targets. This, in turn, allows the mapping of the infection in tissues to better understand viral pathogenesis and replication at the single-cell level. Coupling this method with immunofluorescence may facilitate better understanding of host-virus interactions, including alternation of the host epigenome and immune response pathways. Owing to sensitive and specific HCR technology, this protocol can also be used as a diagnostic tool. It is also important to remember that the technique may be modified easily to enable detection of any RNA, including non-coding RNAs and RNA viruses that may emerge in the future.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Viral / Respiratory Mucosa / COVID-19 Testing / SARS-CoV-2 / COVID-19 Type of study: Diagnostic study Limits: Animals / Humans Language: English Year: 2020 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Viral / Respiratory Mucosa / COVID-19 Testing / SARS-CoV-2 / COVID-19 Type of study: Diagnostic study Limits: Animals / Humans Language: English Year: 2020 Document Type: Article