TY - JOUR
T1 - Sensitive visualization of SARS-CoV-2 RNA with CoronaFISH
AU - Rensen, Elena
AU - Pietropaoli, Stefano
AU - Mueller, Florian
AU - Weber, Christian
AU - Souquere, Sylvie
AU - Sommer, Sina
AU - Isnard, Pierre
AU - Rabant, Marion
AU - Gibier, Jean Baptiste
AU - Terzi, Fabiola
AU - Simon-Loriere, Etienne
AU - Rameix-Welti, Marie Anne
AU - Pierron, Gérard
AU - Barba-Spaeth, Giovanna
AU - Zimmer, Christophe
N1 - Publisher Copyright:
© 2022 Rensen et al.
PY - 2022/4/1
Y1 - 2022/4/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85123268236&partnerID=8YFLogxK
U2 - 10.26508/lsa.202101124
DO - 10.26508/lsa.202101124
M3 - Article
C2 - 34996842
AN - SCOPUS:85123268236
SN - 2575-1077
VL - 5
JO - Life Science Alliance
JF - Life Science Alliance
IS - 4
M1 - 202101124
ER -