Journal of the American Chemical Society · 2021 · 89 citations · 16 references
EngineeringViral DiagnosticsMolecular BiologyNucleic Acid Amplification TestNucleic Acid BiomarkersCovid-19Isothermal Amplification StrategiesViral PathogenMolecular DiagnosticsVirologyBioinformaticsMolecular Diagnostic TechniquesEmerging Infectious DiseasesAnalyte PreamplificationNucleic Acid BiochemistryNucleic Acid AmplificationMicrobiologySystems BiologyMedicine
Isothermal amplification strategies capable of rapid, inexpensive, and accurate nucleic acid detection provide new options for large-scale pathogen detection, disease diagnosis, and genotyping. Here we report a highly sensitive multicomponent XNA-based nucleic acid detection platform that combines analyte preamplification with X10–23-mediated catalysis to detect the viral pathogen responsible for COVID-19. The platform, termed RNA-Encoded Viral Nucleic Acid Analyte Reporter (REVEALR), functions with a detection limit of ≤20 aM (∼10 copies/μL) using conventional fluorescence and paper-based lateral flow readout modalities. With a total assay time of 1 h, REVEALR provides a convenient nucleic acid alternative to equivalent CRISPR-based approaches, which have become popular methods for SARS-CoV-2 detection. The assay shows no cross-reactivity for other in vitro transcribed respiratory viral RNAs and functions with perfect accuracy against COVID-19 patient-derived clinical samples.
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Loop-mediated isothermal amplification of DNA
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CRISPR–Cas12-based detection of SARS-CoV-2
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