Digital assay for rapid electronic quantification of clinical pathogens using DNA nanoballs.
Muhammad TayyabDonal BarrettGijs van RielShujing LiuBjörn ReiniusCurt ScharfePeter GriffinLars M SteinmetzMehdi JavanmardVicent PelechanoPublished in: Science advances (2023)
Fast and accurate detection of nucleic acids is key for pathogen identification. Methods for DNA detection generally rely on fluorescent or colorimetric readout. The development of label-free assays decreases costs and test complexity. We present a novel method combining a one-pot isothermal generation of DNA nanoballs with their detection by electrical impedance. We modified loop-mediated isothermal amplification by using compaction oligonucleotides that self-assemble the amplified target into nanoballs. Next, we use capillary-driven flow to passively pass these nanoballs through a microfluidic impedance cytometer, thus enabling a fully compact system with no moving parts. The movement of individual nanoballs is detected by a change in impedance providing a quantized readout. This approach is flexible for the detection of DNA/RNA of numerous targets (severe acute respiratory syndrome coronavirus 2, HIV, β-lactamase gene, etc.), and we anticipate that its integration into a standalone device would provide an inexpensive (<$5), sensitive (10 target copies), and rapid test (<1 hour).
Keyphrases
- loop mediated isothermal amplification
- label free
- sensitive detection
- circulating tumor
- nucleic acid
- cell free
- single molecule
- respiratory syndrome coronavirus
- quantum dots
- high throughput
- sars cov
- escherichia coli
- gold nanoparticles
- human immunodeficiency virus
- multidrug resistant
- circulating tumor cells
- hiv infected
- living cells
- hepatitis c virus
- real time pcr
- gram negative
- gene expression
- magnetic resonance imaging
- copy number
- transcription factor
- south africa
- dna methylation