Cargando…
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...
Autores principales: | , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783496284615737344 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7012833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT wangxinjie crisprcas12atechnologycombinedwithimmunochromatographicstripsforportabledetectionofafricanswinefevervirus AT jipinpin crisprcas12atechnologycombinedwithimmunochromatographicstripsforportabledetectionofafricanswinefevervirus AT fanhuiying crisprcas12atechnologycombinedwithimmunochromatographicstripsforportabledetectionofafricanswinefevervirus AT danglu crisprcas12atechnologycombinedwithimmunochromatographicstripsforportabledetectionofafricanswinefevervirus AT wanwenwei crisprcas12atechnologycombinedwithimmunochromatographicstripsforportabledetectionofafricanswinefevervirus AT liusiyuan crisprcas12atechnologycombinedwithimmunochromatographicstripsforportabledetectionofafricanswinefevervirus AT liyanhua crisprcas12atechnologycombinedwithimmunochromatographicstripsforportabledetectionofafricanswinefevervirus AT yuwenxia crisprcas12atechnologycombinedwithimmunochromatographicstripsforportabledetectionofafricanswinefevervirus AT lixiangyang crisprcas12atechnologycombinedwithimmunochromatographicstripsforportabledetectionofafricanswinefevervirus AT maxiaodong crisprcas12atechnologycombinedwithimmunochromatographicstripsforportabledetectionofafricanswinefevervirus AT maxu crisprcas12atechnologycombinedwithimmunochromatographicstripsforportabledetectionofafricanswinefevervirus AT zhaoqin crisprcas12atechnologycombinedwithimmunochromatographicstripsforportabledetectionofafricanswinefevervirus AT huangxingxu crisprcas12atechnologycombinedwithimmunochromatographicstripsforportabledetectionofafricanswinefevervirus AT liaoming crisprcas12atechnologycombinedwithimmunochromatographicstripsforportabledetectionofafricanswinefevervirus |