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CRISPR/Cas12a technology combined with immunochromatographic strips for portable detection of African swine fever virus

African swine fever virus (ASFV), the aetiological agent of African swine fever (ASF), causes lethal haemorrhagic fever in domestic pigs with high mortality and morbidity and has devastating consequences on the global swine industry. On-site rapid and sensitive detection of ASFV is key to the timely...

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Autores principales: Wang, Xinjie, Ji, Pinpin, Fan, Huiying, Dang, Lu, Wan, Wenwei, Liu, Siyuan, Li, Yanhua, Yu, Wenxia, Li, Xiangyang, Ma, Xiaodong, Ma, Xu, Zhao, Qin, Huang, Xingxu, Liao, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012833/
https://www.ncbi.nlm.nih.gov/pubmed/32047240
http://dx.doi.org/10.1038/s42003-020-0796-5
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author Wang, Xinjie
Ji, Pinpin
Fan, Huiying
Dang, Lu
Wan, Wenwei
Liu, Siyuan
Li, Yanhua
Yu, Wenxia
Li, Xiangyang
Ma, Xiaodong
Ma, Xu
Zhao, Qin
Huang, Xingxu
Liao, Ming
author_facet Wang, Xinjie
Ji, Pinpin
Fan, Huiying
Dang, Lu
Wan, Wenwei
Liu, Siyuan
Li, Yanhua
Yu, Wenxia
Li, Xiangyang
Ma, Xiaodong
Ma, Xu
Zhao, Qin
Huang, Xingxu
Liao, Ming
author_sort Wang, Xinjie
collection PubMed
description African swine fever virus (ASFV), the aetiological agent of African swine fever (ASF), causes lethal haemorrhagic fever in domestic pigs with high mortality and morbidity and has devastating consequences on the global swine industry. On-site rapid and sensitive detection of ASFV is key to the timely implementation of control. In this study, we developed a rapid, sensitive and instrument-free ASFV detection method based on CRISPR/Cas12a technology and lateral flow detection (named CRISPR/Cas12a-LFD). The limit of detection of CRISPR/Cas12a-LFD is 20 copies of ASFV genomic DNA per reaction, and the detection process can be completed in an hour. The assay showed no cross-reactivity with other swine DNA viruses, and has 100% agreement with real-time PCR detection of ASFV in 149 clinical samples. Overall, the CRISPR/Cas12a-LFD method provides a novel alternative for the portable, simple, sensitive, and specific detection of ASFV and may contribute to the prevention and control of ASF outbreaks.
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spelling pubmed-70128332020-03-03 CRISPR/Cas12a technology combined with immunochromatographic strips for portable detection of African swine fever virus Wang, Xinjie Ji, Pinpin Fan, Huiying Dang, Lu Wan, Wenwei Liu, Siyuan Li, Yanhua Yu, Wenxia Li, Xiangyang Ma, Xiaodong Ma, Xu Zhao, Qin Huang, Xingxu Liao, Ming Commun Biol Article African swine fever virus (ASFV), the aetiological agent of African swine fever (ASF), causes lethal haemorrhagic fever in domestic pigs with high mortality and morbidity and has devastating consequences on the global swine industry. On-site rapid and sensitive detection of ASFV is key to the timely implementation of control. In this study, we developed a rapid, sensitive and instrument-free ASFV detection method based on CRISPR/Cas12a technology and lateral flow detection (named CRISPR/Cas12a-LFD). The limit of detection of CRISPR/Cas12a-LFD is 20 copies of ASFV genomic DNA per reaction, and the detection process can be completed in an hour. The assay showed no cross-reactivity with other swine DNA viruses, and has 100% agreement with real-time PCR detection of ASFV in 149 clinical samples. Overall, the CRISPR/Cas12a-LFD method provides a novel alternative for the portable, simple, sensitive, and specific detection of ASFV and may contribute to the prevention and control of ASF outbreaks. Nature Publishing Group UK 2020-02-11 /pmc/articles/PMC7012833/ /pubmed/32047240 http://dx.doi.org/10.1038/s42003-020-0796-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wang, Xinjie
Ji, Pinpin
Fan, Huiying
Dang, Lu
Wan, Wenwei
Liu, Siyuan
Li, Yanhua
Yu, Wenxia
Li, Xiangyang
Ma, Xiaodong
Ma, Xu
Zhao, Qin
Huang, Xingxu
Liao, Ming
CRISPR/Cas12a technology combined with immunochromatographic strips for portable detection of African swine fever virus
title CRISPR/Cas12a technology combined with immunochromatographic strips for portable detection of African swine fever virus
title_full CRISPR/Cas12a technology combined with immunochromatographic strips for portable detection of African swine fever virus
title_fullStr CRISPR/Cas12a technology combined with immunochromatographic strips for portable detection of African swine fever virus
title_full_unstemmed CRISPR/Cas12a technology combined with immunochromatographic strips for portable detection of African swine fever virus
title_short CRISPR/Cas12a technology combined with immunochromatographic strips for portable detection of African swine fever virus
title_sort crispr/cas12a technology combined with immunochromatographic strips for portable detection of african swine fever virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012833/
https://www.ncbi.nlm.nih.gov/pubmed/32047240
http://dx.doi.org/10.1038/s42003-020-0796-5
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