Cargando…

A one-pot CRISPR/Cas13a-based contamination-free biosensor for low-cost and rapid nucleic acid diagnostics

The pandemic due to the outbreak of 2019 coronavirus disease (COVID-19) caused by novel severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has raised significant public health concerns. Rapid, affordable, and accurate diagnostic testing not only paves the way for the effective treatment of...

Descripción completa

Detalles Bibliográficos
Autores principales: Hu, Fei, Liu, Yanfei, Zhao, Shuhao, Zhang, Zengming, Li, Xichen, Peng, Niancai, Jiang, Zhuangde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755463/
https://www.ncbi.nlm.nih.gov/pubmed/35042129
http://dx.doi.org/10.1016/j.bios.2022.113994
_version_ 1784632387447029760
author Hu, Fei
Liu, Yanfei
Zhao, Shuhao
Zhang, Zengming
Li, Xichen
Peng, Niancai
Jiang, Zhuangde
author_facet Hu, Fei
Liu, Yanfei
Zhao, Shuhao
Zhang, Zengming
Li, Xichen
Peng, Niancai
Jiang, Zhuangde
author_sort Hu, Fei
collection PubMed
description The pandemic due to the outbreak of 2019 coronavirus disease (COVID-19) caused by novel severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has raised significant public health concerns. Rapid, affordable, and accurate diagnostic testing not only paves the way for the effective treatment of diseases, but also plays a crucial role in preventing the spreading of infectious diseases. Herein, a one-pot CRISPR/Cas13a-based visual biosensor was proposed and developed for the rapid and low-cost nucleic acid detection. By combining Cas13a cleavage and Recombinase Polymerase Amplification (RPA) in a one-pot reaction in a disposable tube-in-tube vessel, amplicon contamination could be completely avoided. The RPA reaction is carried out in the inner tube containing two hydrophobic holes at the bottom. After the completion of amplification reaction, the reaction solution enters the outer tube containing pre-stored Cas13a reagent under the action of centrifugation or shaking. Inner and outer tubes are combined to form an independent reaction pot to complete the nucleic acid detection without opening the lid. This newly developed nucleic acid detection method not only meets the need of rapid nucleic acid detection at home without the need for any specialized equipment, but also fulfils the requirement of rapid on-site nucleic acid detection with the aid of small automated instruments. In this study, CRISPR/Cas13a and CRISPR/Cas12a were used to verify the reliability of the developed one-pot nucleic acid detection method. The performance of the system was verified by detecting the DNA virus, i.e., African swine fever virus (ASFV) and the RNA virus, i.e., SARS-Cov-2. The results indicate that the proposed method possesses a limit of detection of 3 copy/μL. The negative and positive test results are consistent with the results of real-time fluorescence quantitative polymerase chain reaction (PCR), but the time required is shorter and the cost is lower. Thus, this study makes this method available in resource-limited areas for the purpose of large-scale screening and in case of epidemic outbreak.
format Online
Article
Text
id pubmed-8755463
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier B.V.
record_format MEDLINE/PubMed
spelling pubmed-87554632022-01-13 A one-pot CRISPR/Cas13a-based contamination-free biosensor for low-cost and rapid nucleic acid diagnostics Hu, Fei Liu, Yanfei Zhao, Shuhao Zhang, Zengming Li, Xichen Peng, Niancai Jiang, Zhuangde Biosens Bioelectron Article The pandemic due to the outbreak of 2019 coronavirus disease (COVID-19) caused by novel severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has raised significant public health concerns. Rapid, affordable, and accurate diagnostic testing not only paves the way for the effective treatment of diseases, but also plays a crucial role in preventing the spreading of infectious diseases. Herein, a one-pot CRISPR/Cas13a-based visual biosensor was proposed and developed for the rapid and low-cost nucleic acid detection. By combining Cas13a cleavage and Recombinase Polymerase Amplification (RPA) in a one-pot reaction in a disposable tube-in-tube vessel, amplicon contamination could be completely avoided. The RPA reaction is carried out in the inner tube containing two hydrophobic holes at the bottom. After the completion of amplification reaction, the reaction solution enters the outer tube containing pre-stored Cas13a reagent under the action of centrifugation or shaking. Inner and outer tubes are combined to form an independent reaction pot to complete the nucleic acid detection without opening the lid. This newly developed nucleic acid detection method not only meets the need of rapid nucleic acid detection at home without the need for any specialized equipment, but also fulfils the requirement of rapid on-site nucleic acid detection with the aid of small automated instruments. In this study, CRISPR/Cas13a and CRISPR/Cas12a were used to verify the reliability of the developed one-pot nucleic acid detection method. The performance of the system was verified by detecting the DNA virus, i.e., African swine fever virus (ASFV) and the RNA virus, i.e., SARS-Cov-2. The results indicate that the proposed method possesses a limit of detection of 3 copy/μL. The negative and positive test results are consistent with the results of real-time fluorescence quantitative polymerase chain reaction (PCR), but the time required is shorter and the cost is lower. Thus, this study makes this method available in resource-limited areas for the purpose of large-scale screening and in case of epidemic outbreak. Elsevier B.V. 2022-04-15 2022-01-13 /pmc/articles/PMC8755463/ /pubmed/35042129 http://dx.doi.org/10.1016/j.bios.2022.113994 Text en © 2022 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
Hu, Fei
Liu, Yanfei
Zhao, Shuhao
Zhang, Zengming
Li, Xichen
Peng, Niancai
Jiang, Zhuangde
A one-pot CRISPR/Cas13a-based contamination-free biosensor for low-cost and rapid nucleic acid diagnostics
title A one-pot CRISPR/Cas13a-based contamination-free biosensor for low-cost and rapid nucleic acid diagnostics
title_full A one-pot CRISPR/Cas13a-based contamination-free biosensor for low-cost and rapid nucleic acid diagnostics
title_fullStr A one-pot CRISPR/Cas13a-based contamination-free biosensor for low-cost and rapid nucleic acid diagnostics
title_full_unstemmed A one-pot CRISPR/Cas13a-based contamination-free biosensor for low-cost and rapid nucleic acid diagnostics
title_short A one-pot CRISPR/Cas13a-based contamination-free biosensor for low-cost and rapid nucleic acid diagnostics
title_sort one-pot crispr/cas13a-based contamination-free biosensor for low-cost and rapid nucleic acid diagnostics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755463/
https://www.ncbi.nlm.nih.gov/pubmed/35042129
http://dx.doi.org/10.1016/j.bios.2022.113994
work_keys_str_mv AT hufei aonepotcrisprcas13abasedcontaminationfreebiosensorforlowcostandrapidnucleicaciddiagnostics
AT liuyanfei aonepotcrisprcas13abasedcontaminationfreebiosensorforlowcostandrapidnucleicaciddiagnostics
AT zhaoshuhao aonepotcrisprcas13abasedcontaminationfreebiosensorforlowcostandrapidnucleicaciddiagnostics
AT zhangzengming aonepotcrisprcas13abasedcontaminationfreebiosensorforlowcostandrapidnucleicaciddiagnostics
AT lixichen aonepotcrisprcas13abasedcontaminationfreebiosensorforlowcostandrapidnucleicaciddiagnostics
AT pengniancai aonepotcrisprcas13abasedcontaminationfreebiosensorforlowcostandrapidnucleicaciddiagnostics
AT jiangzhuangde aonepotcrisprcas13abasedcontaminationfreebiosensorforlowcostandrapidnucleicaciddiagnostics
AT hufei onepotcrisprcas13abasedcontaminationfreebiosensorforlowcostandrapidnucleicaciddiagnostics
AT liuyanfei onepotcrisprcas13abasedcontaminationfreebiosensorforlowcostandrapidnucleicaciddiagnostics
AT zhaoshuhao onepotcrisprcas13abasedcontaminationfreebiosensorforlowcostandrapidnucleicaciddiagnostics
AT zhangzengming onepotcrisprcas13abasedcontaminationfreebiosensorforlowcostandrapidnucleicaciddiagnostics
AT lixichen onepotcrisprcas13abasedcontaminationfreebiosensorforlowcostandrapidnucleicaciddiagnostics
AT pengniancai onepotcrisprcas13abasedcontaminationfreebiosensorforlowcostandrapidnucleicaciddiagnostics
AT jiangzhuangde onepotcrisprcas13abasedcontaminationfreebiosensorforlowcostandrapidnucleicaciddiagnostics