4.8 Article

Paper Device Combining CRISPR/Cas12a and Reverse-Transcription Loop-Mediated Isothermal Amplification for SARS-CoV-2 Detection in Wastewater

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume -, Issue -, Pages -

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.2c04727

Keywords

SARS-CoV-2; CRISPR; Cas12a; RT-LAMP; paper device; wastewater

Funding

  1. National Natural Science Foundation of China [42107486]
  2. Guizhou Provincial Science and Technology Projects [JCTD-2021-17, KFJ-STS-QYZD-185]
  3. Youth Cross Team Project of CAS [NE/R013349/2]
  4. STS of CAS [NE/V010441/1]
  5. UK NERC Fellowship
  6. N-WESP
  7. [Qian-kehe Zhicheng [2020] 4Y190]
  8. [Qiankehe Jichu-ZK [2022] Yiban 565]

Ask authors/readers for more resources

A portable paper device based on CRISPR/Cas12a and RT-LAMP was developed for the detection of SARS-CoV-2 in wastewater, offering high sensitivity and specificity. The device enables simultaneous detection of the N, E, and S genes through different visualization pathways, and provides semi-quantitative analysis. This study demonstrates a promising point-of-use method for wastewater-based surveillance.
Wastewater-based surveillance of the COVID-19 pan-demic holds great promise; however, a point-of-use detection method for SARS-CoV-2 in wastewater is lacking. Here, a portable paper device based on CRISPR/Cas12a and reverse-transcription loop-mediated isothermal amplification (RT-LAMP) with excellent sensitivity and specificity was developed for SARS-CoV-2 detection in wastewater. Three primer sets of RT-LAMP and guide RNAs (gRNAs) that could lead Cas12a to recognize target genes via base pairing were used to perform the high-fidelity RT-LAMP to detect the N, E, and S genes of SARS-CoV-2. Due to the trans-cleavage activity of CRISPR/Cas12a after high-fidelity amplicon recognition, carboxyfluorescein-ssDNA-Black Hole Quencher-1 and carboxyfluorescein-ssDNA-biotin probes were adopted to realize different visualization pathways via a fluorescence or lateral flow analysis, respectively. The reactions were integrated into a paper device for simultaneously detecting the N, E, and S genes with limits of detection (LODs) of 25, 310, and 10 copies/mL, respectively. The device achieved a semiquantitative analysis from 0 to 310 copies/mL due to the different LODs of the three genes. Blind experiments demonstrated that the device was suitable for wastewater analysis with 97.7% sensitivity and 82% semiquantitative accuracy. This is the first semiquantitative endpoint detection of SARS-CoV-2 in wastewater via different LODs, demonstrating a promising point-of-use method for wastewater-based surveillance.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available