Abstract
The COVID-19 pandemic has strained healthcare systems. Sensitive, specific, and timely COVID-19 diagnosis is crucial for effective medical intervention and transmission control. RT-PCR is the most sensitive/specific, but requires costly equipment and trained personnel in centralized laboratories, which are inaccessible to resource-limited areas. Antigen rapid tests enable point-of-care (POC) detection but are significantly less sensitive/specific. CRISPR-Cas systems are compatible with isothermal amplification and dipstick readout, enabling sensitive/specific on-site testing. However, improvements in sensitivity and workflow complexity are needed to spur clinical adoption. We outline the mechanisms/strategies of major CRISPR-Cas systems, evaluate their on-site diagnostic capabilities, and discuss future research directions.
| Original language | English |
|---|---|
| Pages (from-to) | 1346-1360 |
| Number of pages | 15 |
| Journal | Trends in Biotechnology |
| Volume | 40 |
| Issue number | 11 |
| DOIs | |
| State | Published - Nov 2022 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2022 Elsevier Ltd
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- CRISPR-Cas
- Cas12/13
- RNA/DNA detection
- diagnostics
- infectious diseases
- point-of-care
ASJC Scopus subject areas
- Biotechnology
- Bioengineering
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