A plasmid DNA-launched SARS-CoV-2 reverse genetics system and coronavirus toolkit for COVID-19 research.
A549 Cells
Angiotensin-Converting Enzyme 2
/ metabolism
Animals
COVID-19
/ diagnosis
COVID-19 Vaccines
Chlorocebus aethiops
Codon
Humans
Hydrazones
/ pharmacology
Mice
Morpholines
/ pharmacology
Open Reading Frames
Plasmids
/ genetics
Pyrimidines
/ pharmacology
Reverse Genetics
SARS-CoV-2
/ genetics
Serine Endopeptidases
/ metabolism
Vero Cells
Viral Proteins
/ metabolism
Journal
PLoS biology
ISSN: 1545-7885
Titre abrégé: PLoS Biol
Pays: United States
ID NLM: 101183755
Informations de publication
Date de publication:
02 2021
02 2021
Historique:
received:
01
09
2020
accepted:
05
01
2021
entrez:
25
2
2021
pubmed:
26
2
2021
medline:
16
3
2021
Statut:
epublish
Résumé
The recent emergence of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), the underlying cause of Coronavirus Disease 2019 (COVID-19), has led to a worldwide pandemic causing substantial morbidity, mortality, and economic devastation. In response, many laboratories have redirected attention to SARS-CoV-2, meaning there is an urgent need for tools that can be used in laboratories unaccustomed to working with coronaviruses. Here we report a range of tools for SARS-CoV-2 research. First, we describe a facile single plasmid SARS-CoV-2 reverse genetics system that is simple to genetically manipulate and can be used to rescue infectious virus through transient transfection (without in vitro transcription or additional expression plasmids). The rescue system is accompanied by our panel of SARS-CoV-2 antibodies (against nearly every viral protein), SARS-CoV-2 clinical isolates, and SARS-CoV-2 permissive cell lines, which are all openly available to the scientific community. Using these tools, we demonstrate here that the controversial ORF10 protein is expressed in infected cells. Furthermore, we show that the promising repurposed antiviral activity of apilimod is dependent on TMPRSS2 expression. Altogether, our SARS-CoV-2 toolkit, which can be directly accessed via our website at https://mrcppu-covid.bio/, constitutes a resource with considerable potential to advance COVID-19 vaccine design, drug testing, and discovery science.
Identifiants
pubmed: 33630831
doi: 10.1371/journal.pbio.3001091
pii: PBIOLOGY-D-20-02646
pmc: PMC7906417
doi:
Substances chimiques
COVID-19 Vaccines
0
Codon
0
Hydrazones
0
Morpholines
0
Pyrimidines
0
Viral Proteins
0
ACE2 protein, human
EC 3.4.17.23
Angiotensin-Converting Enzyme 2
EC 3.4.17.23
Serine Endopeptidases
EC 3.4.21.-
TMPRSS2 protein, human
EC 3.4.21.-
apilimod
GFW2K84S4L
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e3001091Subventions
Organisme : Medical Research Council
ID : MR/T029188/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12014/12
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/P022642/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_19026
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 201366/Z/16/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12014/2
Pays : United Kingdom
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12014/10
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_20034
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/K024752/1
Pays : United Kingdom
Organisme : Bill & Melinda Gates Foundation
ID : INV-016128
Pays : United States
Organisme : Medical Research Council
ID : MR/V03541X/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_00018/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12014/8
Pays : United Kingdom
Déclaration de conflit d'intérêts
The authors have declared that no competing interests exist.
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