4.8 Article

Extraction of Viral Nucleic Acids with Carbon Nanotubes Increases SARS-CoV-2 Quantitative Reverse Transcription Polymerase Chain Reaction Detection Sensitivity

期刊

ACS NANO
卷 15, 期 6, 页码 10309-10317

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.1c02494

关键词

viral diagnostics; qPCR; DNA/RNA extraction; carbon nanotubes; nanotechnology; nanosensors

资金

  1. IGI LGR ERA
  2. GlaxoSmithKline
  3. Burroughs Wellcome Fund Career Award at the Scientific Interface (CASI)
  4. Dreyfus foundation award
  5. Stanley Fahn PDF Junior Faculty Grant [PF-JFA-1760]
  6. Beckman Foundation Young Investigator Award
  7. NIH MIRA award
  8. NSF CAREER award
  9. NSF CBET award
  10. NSF CGEM award
  11. Sloan Foundation Award
  12. USDA BBT EAGER award
  13. USDA NIFA award
  14. Moore Foundation Award
  15. Cisco Research Center grant
  16. DARPA Young Investigator Award
  17. Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy [DE-AC02-05CH11231]
  18. NSF [NSF DGE 1752814]
  19. Citris/Banatao Seed Funding
  20. FFAR Young Investigator award
  21. CZI investigator award

向作者/读者索取更多资源

The global SARS-CoV-2 pandemic has driven a surge in demand for rapid and efficient viral infection diagnostic tests, leading to a shortage in diagnostic test consumables. A new method using carbon nanotubes and ssDNA sequences has been developed to achieve high-yield extraction of viral nucleic acids, with a 100% extraction yield of target SARS-CoV-2 RNA. This method allows direct extraction of nucleic acids from human saliva, bypassing the need for further biofluid purification and commercial extraction kits.
The global SARS-CoV-2 coronavirus pandemic has led to a surging demand for rapid and efficient viral infection diagnostic tests, generating a supply shortage in diagnostic test consumables including nucleic acid extraction kits. Here, we develop a modular method for high-yield extraction of viral single-stranded nucleic acids by using capture ssDNA sequences attached to carbon nanotubes. Target SARS-CoV-2 viral RNA can be captured by ssDNA-nanotube constructs via hybridization and separated from the liquid phase in a single-tube system with minimal chemical reagents, for downstream quantitative reverse transcription polymerase chain reaction (RT-qPCR) detection. This nanotube-based extraction method enables 100% extraction yield of target SARS-CoV-2 RNA from phosphate-buffered saline in comparison to similar to 20% extraction yield when using a commercial silica-column kit. Notably, carbon nanotubes enable extraction of nucleic acids directly from 50% human saliva with a similar efficiency as achieved with commercial DNA/RNA extraction kits, thereby bypassing the need for further biofluid purification and avoiding the use of commercial extraction kits. Carbon nanotube-based extraction of viral nucleic acids facilitates high-yield and high-sensitivity identification of viral nucleic acids such as the SARS-CoV-2 viral genome with a reduced reliance on reagents affected by supply chain obstacles.

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