dc.date.accessioned | 2023-04-03T19:43:27Z | |
dc.date.available | 2023-04-03T19:43:27Z | |
dc.date.issued | 2022-11-11 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/150365 | |
dc.description.abstract | Point-of-care (POC) nucleic acid detection technologies are poised to aid gold-standard technologies in controlling the COVID-19 pandemic, yet shortcomings in the capability to perform critically needed complex detection-such as multiplexed detection for viral variant surveillance-may limit their widespread adoption. Herein, we developed a robust multiplexed clustered regularly interspaced short palindromic repeats (CRISPR)-based detection using LwaCas13a and PsmCas13b to simultaneously diagnose severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and pinpoint the causative SARS-CoV-2 variant of concern (VOC)-including globally dominant VOCs Delta (B.1.617.2) and Omicron (B.1.1.529)-all the while maintaining high levels of accuracy upon the detection of multiple SARS-CoV-2 gene targets. The platform has several attributes suitable for POC use: premixed, freeze-dried reagents for easy use and storage; convenient direct-to-eye or smartphone-based readouts; and a one-pot variant of the multiplexed detection. To reduce reliance on proprietary reagents and enable sustainable use of such a technology in low- and middle-income countries, we locally produced and formulated our own recombinase polymerase amplification reaction and demonstrated its equivalent efficiency to commercial counterparts. Our tool-CRISPR-based detection for simultaneous COVID-19 diagnosis and variant surveillance that can be locally manufactured-may enable sustainable use of CRISPR diagnostics technologies for COVID-19 and other diseases in POC settings. | en_US |
dc.language.iso | en | |
dc.publisher | Mary Ann Liebert Inc | en_US |
dc.relation.isversionof | 10.1089/crispr.2022.0048 | en_US |
dc.rights | Creative Commons Attribution-Noncommercial-Share Alike | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-sa/4.0/ | en_US |
dc.source | Imperial College London repository | en_US |
dc.title | A Multiplexed Cas13-Based Assay with Point-of-Care Attributes for Simultaneous COVID-19 Diagnosis and Variant Surveillance | en_US |
dc.type | Article | en_US |
dc.identifier.citation | 2022. "A Multiplexed Cas13-Based Assay with Point-of-Care Attributes for Simultaneous COVID-19 Diagnosis and Variant Surveillance." The CRISPR Journal. | |
dc.contributor.department | Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences | en_US |
dc.relation.journal | The CRISPR Journal | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dc.date.updated | 2023-04-03T19:39:32Z | |
dspace.orderedauthors | Patchsung, M; Homchan, A; Aphicho, K; Suraritdechachai, S; Wanitchanon, T; Pattama, A; Sappakhaw, K; Meesawat, P; Wongsatit, T; Athipanyasilp, A; Jantarug, K; Athipanyasilp, N; Buahom, J; Visanpattanasin, S; Niljianskul, N; Chaiyen, P; Tinikul, R; Wichukchinda, N; Mahasirimongkol, S; Sirijatuphat, R; Angkasekwinai, N; Crone, MA; Freemont, PS; Joung, J; Ladha, A; Abudayyeh, O; Gootenberg, J; Zhang, F; Chewapreecha, C; Chanarat, S; Horthongkham, N; Pakotiprapha, D; Uttamapinant, C | en_US |
dspace.date.submission | 2023-04-03T19:39:35Z | |
mit.license | OPEN_ACCESS_POLICY | |
mit.metadata.status | Authority Work and Publication Information Needed | en_US |