Publicación: Clinical validation of RCSMS: A rapid and sensitive CRISPR-Cas12a test for the molecular detection of SARS-CoV-2 from saliva
| dc.contributor.author | del Prado, Joaquín Abugattas-Núñez | |
| dc.contributor.author | Reyes, Angélica Quintana | |
| dc.contributor.author | Leon, Julio | |
| dc.contributor.author | Torre, Juan Blume La | |
| dc.contributor.author | Loli, Renzo Gutiérrez | |
| dc.contributor.author | Olejua, Alejandro Pinzón | |
| dc.contributor.author | Chirinos, Elena Rocío Chamorro | |
| dc.contributor.author | Mauricio, Félix Antonio Loza | |
| dc.contributor.author | Maguiña, Jorge L. | |
| dc.contributor.author | Rodriguez-Aliaga, Piere | |
| dc.contributor.author | Málaga-Trillo, Edward | |
| dc.date.accessioned | 2026-05-01T06:26:59Z | |
| dc.date.issued | 2024 | |
| dc.description.abstract | Peru's holds the highest COVID death rate per capita worldwide. Key to this outcome is the lack of robust, rapid, and accurate molecular tests to circumvent the elevated costs and logistics of SARS-CoV-2 detection via RT-qPCR. To facilitate massive and timely COVID-19 testing in rural and socioeconomically deprived contexts, we implemented and validated RCSMS, a rapid and sensitive CRISPR-Cas12a test for the molecular detection of SARS-CoV-2 from saliva. RCSMS uses the power of CRISPR-Cas technology and lateral flow strips to easily visualize the presence of SARS-CoV-2 even in laboratories with limited equipment. We show that a low-cost thermochemical treatment with TCEP/EDTA is sufficient to inactivate viral particles and cellular nucleases in saliva, eliminating the need to extract viral RNA with commercial kits, as well as the cumbersome nasopharyngeal swab procedure and the requirement of biosafety level 2 laboratories for molecular analyses. Notably, RCSMS performed outstandingly in a clinical validation done with 352 patients from two hospitals in Lima, detecting as low as 50 viral copies per 10 μl reaction in 40 min, with sensitivity and specificity of 96.5% and 99.0%, respectively, relative to RT-qPCR. The negative and positive predicted values obtained from this field validation indicate that RCSMS can be confidently deployed in both high and low prevalence settings. Like other CRISPR-Cas-based biosensors, RCSMS can be easily reprogrammed for the detection of new SARS-CoV-2 variants. We conclude that RCSMS is a fast, efficient and inexpensive alternative to RT-qPCR for expanding COVID-19 testing capacity in Peru and other low- and middle-income countries with precarious healthcare systems. Copyright: © 2024 Abugattas-Núñez del Prado et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | en_US |
| dc.description.sponsorship | This study was funded by Concejo Nacional de Ciencia, Tecnología e Innovación Tecnológica (https://www.perucris.pe/home) to author PEMT (grant numbers 111-2020-FONDECYT, 042-2020-FONDECYT, and 113-2020-FONDECYT), Spanish Agency for International Development Cooperation (AECID) (https://www. aecid.es/) to author PEMT (grant number AECID-504.2020), a private donation from ISA REP (https://www.isarep.com.pe/) to author PEMT, a private donation from Sociedad Nacional de Minería, Petróleo y Energía (https://www.snmpe. org.pe) to author PEMT, a private donation from Intercorp (https://www.intercorp.com.pe/en), a private donation from Banco Pichincha (https://www.pichincha.com/) to author PEMT, a private donation from Laboratorios AC Farma S.A. (https://www.acfarma.com) to author PEMT, a private donation from Industrias San Miguel (https://group-ism.com/) to author PEMT, a private donation from IBT Peru (https://www.ibtgroup. com/en/peru) to author PEMT, a private donation from FuXion Biotech SAC (https://fuxion.com/pe) to author PEMT, a private donation from Asociación de Galleros del Perú to author PEMT, and a private donation from Essalud - IETSI (https://ietsi.essalud.gob.pe/) to author PEMT. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We are profoundly indebted to: C.M. Caro, A. Rozas, J. Arriola, H. Añaños, J.C., F. León-Velarde, A. Sobarzo and especially M. and E. Arias for their generous support to this project, from the search for funding sources to assistance with the resolution of regulatory and bureaucratic hurdles. C. Guerra for providing personnel, equipment and reagents, as well as support with administrative procedures. P. Soto for critical reading of the manuscript. T. Ochoa and D. Durand for the use of their laboratory equipment. P. Tsukayama for his help with bioinformatic analyses. V. Adaui and P. Milón for helpful technical discussions. F. Molinelli, E. Carlín, L. Shica, J. Santillana, J. Amorós, P. Pimentel, C. Bedoya, G. Minaya, Y. Hurtado, R. Araujo, G. Solis and C. Díaz-Vélez from ESSALUD, for organizing and facilitating the collaboration with their hospital network for field studies. K. Valverde, C. Morales, H. Pinedo and R. Álvarez for their valuable work in collecting saliva samples from the participants. The local and international press that helped bring attention and support to this project. Merck del Perú, GenLab del Perú, AC Interlab, La Ensenada, Mased and Ahseco for granting priority access to supplies and equipment. We especially want to express our deepest gratitude to the symptomatic patients who attended the COVID-19 triage areas of Guillermo Almenara and Edgardo Rebagliati National Hospitals, for their generous and selfless participation in this study, despite their precarious condition and the often pressing circumstances; for their words of encouragement towards Peruvian science, and for their great humanity. We dedicate our work to them and their families, hoping that they were able to overcome the disease. Finally, our deep condolences to all those who have lost loved ones during this pandemic. | es_PE |
| dc.identifier.doi | https://doi.org/10.1371/journal.pone.0290466 | |
| dc.identifier.scopus | 2-s2.0-85188846020 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12866/19496 | |
| dc.language.iso | eng | |
| dc.publisher | Public Library of Science | |
| dc.relation.ispartof | urn:issn:1932-6203 | |
| dc.relation.ispartofseries | PLoS ONE | |
| dc.relation.issn | 1932-6203 | |
| dc.rights | http://purl.org/coar/access_right/c_abf2 | |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
| dc.subject | Coronaviruses | en_US |
| dc.subject | Coronaviruses Diagnostics and Prognostics | en_US |
| dc.subject | Emerging Infectious Diseases | en_US |
| dc.subject | Infectious Diseases | en_US |
| dc.title | Clinical validation of RCSMS: A rapid and sensitive CRISPR-Cas12a test for the molecular detection of SARS-CoV-2 from saliva | en_US |
| dc.type | https://purl.org/coar/resource_type/c_2df8fbb1 | |
| dc.type.local | Artículo de revista | |
| dc.type.version | info:eu-repo/semantics/publishedVersion | |
| dspace.entity.type | Publication |
