4.6 Article

Sensitive visualization of SARS-CoV-2 RNA with CoronaFISH

Journal

LIFE SCIENCE ALLIANCE
Volume 5, Issue 4, Pages 1-15

Publisher

LIFE SCIENCE ALLIANCE LLC
DOI: 10.26508/lsa.202101124

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Funding

  1. French Government's Investissement d'Avenir program, INCEPTION' [ANR-16-CONV-0005]
  2. Institut Pasteur Coronavirus task force (don AXA COVID-19 project COVID-SPREAD)
  3. Fondation pour la Recherche Medicale (Equipe FRM) [DEQ 20150331762]
  4. Institut Carnot Pasteur MS
  5. Institut Pasteur

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This article introduces a method using FISH probes to visualize the positive and negative RNA of SARS-CoV-2, and demonstrates its application in animal cells, patient samples, and human tissue. The method is helpful for studying viral replication, screening therapeutic molecules, and diagnostics.
The current COVID-19 pandemic is caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The positivesense single-stranded RNA virus contains a single linear RNA segment that serves as a template for transcription and replication, leading to the synthesis of positive and negative-stranded viral RNA (vRNA) in infected cells. Tools to visualize vRNA directly in infected cells are critical to analyze the viral replication cycle, screen for therapeutic molecules, or study infections in human tissue. Here, we report the design, validation, and initial application of FISH probes to visualize positive or negative RNA of SARS-CoV-2 (CoronaFISH). We demonstrate sensitive visualization of vRNA in African green monkey and several human cell lines, in patient samples and human tissue. We further demonstrate the adaptation of CoronaFISH probes to electron microscopy. We provide all required oligonucleotide sequences, source code to design the probes, and a detailed protocol. We hope that CoronaFISH will complement existing techniques for research on SARS-CoV-2 biology and COVID-19 pathophysiology, drug screening, and diagnostics.

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