tetano
Editor, Senior Moderator
J Hazard Mater
. 2023 Apr 25;454:131487.
doi: 10.1016/j.jhazmat.2023.131487. Online ahead of print. RNA extraction-free workflow integrated with a single-tube CRISPR-Cas-based colorimetric assay for rapid SARS-CoV-2 detection in different environmental matrices
Yuliang Kang[SUP] 1 [/SUP], Jiali Wang[SUP] 2 [/SUP], Wensi Zhang[SUP] 2 [/SUP], Yuhang Xu[SUP] 2 [/SUP], Bohui Xu[SUP] 2 [/SUP], Guangbo Qu[SUP] 3 [/SUP], Yanyan Yu[SUP] 4 [/SUP], Bing Yan[SUP] 5 [/SUP], Gaoxing Su[SUP] 6 [/SUP]
Affiliations
On-site environmental surveillance of viruses is increasingly important for infection prevention and pandemic control. Herein, we report a facile single-tube colorimetric assay for detecting severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) from environmental compartments. Using glycerol as the phase separation additive, reverse transcription recombinase polymerase amplification (RT-RPA), CRISPR-Cas system activation, G-quadruplex (G4) cleavage, and G4-based colorimetric reaction were performed in a single tube. To further simplify the test, viral RNA genomes used for the one-tube assay were obtained via acid/base treatment without further purification. The whole assay from sampling to visual readout was completed within 30 min at a constant temperature without the need for sophisticated instruments. Coupling the RT-RPA to CRISPR-Cas improved the reliability by avoiding false positive results. Non-labeled cost-effective G4-based colorimetric systems are highly sensitive to CRISPR-Cas cleavage events, and the proposed assay reached the limit of detection of 0.84 copies/µL. Moreover, environmental samples from contaminated surfaces and wastewater were analyzed using this facile colorimetric assay. Given its simplicity, sensitivity, specificity, and cost-effectiveness, our proposed colorimetric assay is highly promising for applications in on-site environmental surveillance of viruses.
Keywords: CRISPR-Cas; Environmental Surveillance; G-quadruplex; SARS-CoV-2; Virus Detection.
. 2023 Apr 25;454:131487.
doi: 10.1016/j.jhazmat.2023.131487. Online ahead of print. RNA extraction-free workflow integrated with a single-tube CRISPR-Cas-based colorimetric assay for rapid SARS-CoV-2 detection in different environmental matrices
Yuliang Kang[SUP] 1 [/SUP], Jiali Wang[SUP] 2 [/SUP], Wensi Zhang[SUP] 2 [/SUP], Yuhang Xu[SUP] 2 [/SUP], Bohui Xu[SUP] 2 [/SUP], Guangbo Qu[SUP] 3 [/SUP], Yanyan Yu[SUP] 4 [/SUP], Bing Yan[SUP] 5 [/SUP], Gaoxing Su[SUP] 6 [/SUP]
Affiliations
- PMID: 37148798
- DOI: 10.1016/j.jhazmat.2023.131487
On-site environmental surveillance of viruses is increasingly important for infection prevention and pandemic control. Herein, we report a facile single-tube colorimetric assay for detecting severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) from environmental compartments. Using glycerol as the phase separation additive, reverse transcription recombinase polymerase amplification (RT-RPA), CRISPR-Cas system activation, G-quadruplex (G4) cleavage, and G4-based colorimetric reaction were performed in a single tube. To further simplify the test, viral RNA genomes used for the one-tube assay were obtained via acid/base treatment without further purification. The whole assay from sampling to visual readout was completed within 30 min at a constant temperature without the need for sophisticated instruments. Coupling the RT-RPA to CRISPR-Cas improved the reliability by avoiding false positive results. Non-labeled cost-effective G4-based colorimetric systems are highly sensitive to CRISPR-Cas cleavage events, and the proposed assay reached the limit of detection of 0.84 copies/µL. Moreover, environmental samples from contaminated surfaces and wastewater were analyzed using this facile colorimetric assay. Given its simplicity, sensitivity, specificity, and cost-effectiveness, our proposed colorimetric assay is highly promising for applications in on-site environmental surveillance of viruses.
Keywords: CRISPR-Cas; Environmental Surveillance; G-quadruplex; SARS-CoV-2; Virus Detection.