Development and Evaluation of a duo SARS-CoV-2 RT-qPCR Assay Combining Two Assays Approved by the World Health Organization Targeting the Envelope and the RNA-Dependant RNA Polymerase (RdRp) Coding Regions.
Betacoronavirus
/ genetics
COVID-19
Coronavirus Envelope Proteins
Coronavirus Infections
/ diagnosis
Coronavirus RNA-Dependent RNA Polymerase
Humans
Pandemics
Pneumonia, Viral
/ diagnosis
RNA, Viral
/ analysis
RNA-Dependent RNA Polymerase
/ genetics
Real-Time Polymerase Chain Reaction
/ methods
SARS-CoV-2
Sensitivity and Specificity
Viral Envelope Proteins
/ genetics
Viral Nonstructural Proteins
/ genetics
World Health Organization
COVID-19
TaqMan
coronavirus
diagnosis
diagnostics
emerging
molecular
outbreak
preparedness
real-time PCR
respiratory
response
Journal
Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722
Informations de publication
Date de publication:
25 06 2020
25 06 2020
Historique:
received:
05
05
2020
revised:
05
06
2020
accepted:
24
06
2020
entrez:
8
7
2020
pubmed:
8
7
2020
medline:
15
7
2020
Statut:
epublish
Résumé
The recent emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) worldwide has highlighted the importance of reliable and rapid diagnostic testing to prevent and control virus circulation. Dozens of monoplex in-house RT-qPCR assays are already available; however, the development of dual-target assays is suited to avoid false-negative results caused by polymorphisms or point mutations, that can compromise the accuracy of diagnostic and screening tests. In this study, two mono-target assays recommended by WHO (E-Sarbeco (enveloppe gene, Charite University, Berlin, Germany) and RdRp-IP4 (RdRp, Institut Pasteur, Paris, France)) were selected and combined in a unique robust test; the resulting duo SARS-CoV-2 RT-qPCR assay was compared to the two parental monoplex tests. The duo SARS-CoV-2 assay performed equally, or better, in terms of sensitivity, specificity, linearity and signal intensity. We demonstrated that combining two single systems into a dual-target assay (with or without an MS2-based internal control) did not impair performances, providing a potent tool adapted for routine molecular diagnosis in clinical microbiology laboratories.
Identifiants
pubmed: 32630601
pii: v12060686
doi: 10.3390/v12060686
pmc: PMC7354606
pii:
doi:
Substances chimiques
Coronavirus Envelope Proteins
0
RNA, Viral
0
Viral Envelope Proteins
0
Viral Nonstructural Proteins
0
envelope protein, SARS-CoV-2
0
Coronavirus RNA-Dependent RNA Polymerase
EC 2.7.7.48
NSP12 protein, SARS-CoV-2
EC 2.7.7.48
RNA-Dependent RNA Polymerase
EC 2.7.7.48
Types de publication
Comparative Study
Evaluation Study
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : H2020 Research Infrastructures
ID : 871029
Pays : International
Organisme : H2020 Fast Track to Innovation
ID : 101003544
Pays : International
Organisme : H2020 European Institute of Innovation and Technology
ID : 823666
Pays : International
Organisme : Agence Nationale de la Recherche
ID : PREPMedVet
Pays : International
Organisme : Institut National de la Santé et de la Recherche Médicale
ID : Reacting
Pays : International
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