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DNA nanoscaffold-based SARS-CoV-2 detection for COVID-19 diagnosis
COVID-19 pandemic outbreak is the most astounding scene ever experienced in the 21st century. It has been determined to be caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). With the global pandemic, the lack of efficient rapid and accurate molecular diagnostic testing tools has...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387931/ https://www.ncbi.nlm.nih.gov/pubmed/32763826 http://dx.doi.org/10.1016/j.bios.2020.112479 |
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author | Jiao, Jin Duan, Chengjie Xue, Lan Liu, Yunfei Sun, Weihao Xiang, Yang |
author_facet | Jiao, Jin Duan, Chengjie Xue, Lan Liu, Yunfei Sun, Weihao Xiang, Yang |
author_sort | Jiao, Jin |
collection | PubMed |
description | COVID-19 pandemic outbreak is the most astounding scene ever experienced in the 21st century. It has been determined to be caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). With the global pandemic, the lack of efficient rapid and accurate molecular diagnostic testing tools has hindered the public opportunely response to the emerging viral threat. Herein, a DNA nanoscaffold hybrid chain reaction (DNHCR)-based nucleic acid assay strategy is reported for rapid detection of SARS-CoV-2 RNA. In this method, the DNA nanoscaffolds have been first constructed by the self-assembly of long DNA strands and self-quenching probes (H1). Then, the SARS-CoV-2 RNA will initiate the hybridization of H1 and free H2 DNA probes along the nanoscaffold, and an illuminated DNA nanostring is instantly obtained. By taking advantages of the localization design of the H1 probes and the temperature tolerance of the isothermal amplification, the proposed DNHCR method can detect target at short responding time (within 10 min) and mild condition (15 °C–35 °C). Moreover, the reliability of DNHCR method in serum and saliva samples have also been validated. Therefore, DNHCR-based method is expected to provide a simple and faster alternative to the traditional SARS-CoV-2 qRT-PCR assay. |
format | Online Article Text |
id | pubmed-7387931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73879312020-07-29 DNA nanoscaffold-based SARS-CoV-2 detection for COVID-19 diagnosis Jiao, Jin Duan, Chengjie Xue, Lan Liu, Yunfei Sun, Weihao Xiang, Yang Biosens Bioelectron Article COVID-19 pandemic outbreak is the most astounding scene ever experienced in the 21st century. It has been determined to be caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). With the global pandemic, the lack of efficient rapid and accurate molecular diagnostic testing tools has hindered the public opportunely response to the emerging viral threat. Herein, a DNA nanoscaffold hybrid chain reaction (DNHCR)-based nucleic acid assay strategy is reported for rapid detection of SARS-CoV-2 RNA. In this method, the DNA nanoscaffolds have been first constructed by the self-assembly of long DNA strands and self-quenching probes (H1). Then, the SARS-CoV-2 RNA will initiate the hybridization of H1 and free H2 DNA probes along the nanoscaffold, and an illuminated DNA nanostring is instantly obtained. By taking advantages of the localization design of the H1 probes and the temperature tolerance of the isothermal amplification, the proposed DNHCR method can detect target at short responding time (within 10 min) and mild condition (15 °C–35 °C). Moreover, the reliability of DNHCR method in serum and saliva samples have also been validated. Therefore, DNHCR-based method is expected to provide a simple and faster alternative to the traditional SARS-CoV-2 qRT-PCR assay. Elsevier B.V. 2020-11-01 2020-07-29 /pmc/articles/PMC7387931/ /pubmed/32763826 http://dx.doi.org/10.1016/j.bios.2020.112479 Text en © 2020 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Jiao, Jin Duan, Chengjie Xue, Lan Liu, Yunfei Sun, Weihao Xiang, Yang DNA nanoscaffold-based SARS-CoV-2 detection for COVID-19 diagnosis |
title | DNA nanoscaffold-based SARS-CoV-2 detection for COVID-19 diagnosis |
title_full | DNA nanoscaffold-based SARS-CoV-2 detection for COVID-19 diagnosis |
title_fullStr | DNA nanoscaffold-based SARS-CoV-2 detection for COVID-19 diagnosis |
title_full_unstemmed | DNA nanoscaffold-based SARS-CoV-2 detection for COVID-19 diagnosis |
title_short | DNA nanoscaffold-based SARS-CoV-2 detection for COVID-19 diagnosis |
title_sort | dna nanoscaffold-based sars-cov-2 detection for covid-19 diagnosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387931/ https://www.ncbi.nlm.nih.gov/pubmed/32763826 http://dx.doi.org/10.1016/j.bios.2020.112479 |
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