Viral infections are a major global health issue, but no current method allows rapid, direct, and ultrasensitive quantification of intact viruses with the ability to inform infectivity, causing misdiagnoses and spread of the viruses. Here, we report a method for direct detection and differentiation of infectious from noninfectious human adenovirus and SARS-CoV-2, as well as from other virus types, without any sample pretreatment. DNA aptamers are selected from a DNA library to bind intact infectious, but not noninfectious, virus and then incorporated into a solid-state nanopore, which allows strong confinement of the virus to enhance sensitivity down to 1 pfu/ml for human adenovirus and 1 × 10 4 copies/ml for SARS-CoV-2. Applications of the aptamer-nanopore sensors in different types of water samples, saliva, and serum are demonstrated for both enveloped and nonenveloped viruses, making the sensor generally applicable for detecting these and other emerging viruses of environmental and public health concern.
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Electronic Sensors to Detect SARS-CoV-2 Viruses in Real Time
Sensors with 60 nm gap junctions coated with aptamers that bind with S1 and S2 spiking proteins of the SARS-CoV-2 virus were developed. Sensor impedance changes with virus enabling rapid (~1 min), point-of-care detection. Exosomes and other nanoparticles in the saliva produce false positive signals but do not bind with aptamers and are easily removed to achieve 6% false positivity rates. A positive sensor voltage is used to attract the negatively charged SARS-CoV-2 virus to the junction and reduce sensor false negativity rates to below 7%. The limit of detection of the sensor is ~1000 viruses and can be altered by changing sensor’s lateral dimension and its transduction noise level.
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- Award ID(s):
- 2030359
- PAR ID:
- 10379149
- Date Published:
- Journal Name:
- IEEE Sensors Journal
- ISSN:
- 1530-437X
- Page Range / eLocation ID:
- 1 to 1
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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