Cargando…

CRISPR-Cas12a test strip (CRISPR/CAST) package: In-situ detection of Brucella from infected livestock

BACKGROUND: Brucellosis is a common zoonotic disease caused by Brucella, which causes enormous economic losses and public burden to epidemic areas. Early and precise diagnosis and timely culling of infected animals are crucial to prevent the infection and spread of Brucella. In recent years, RNA-gui...

Descripción completa

Detalles Bibliográficos
Autores principales: Dang, Sheng, Sui, Humujile, Zhang, Shuai, Wu, Dongxing, Chen, Zeliang, Zhai, Jingbo, Bai, Meirong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10571365/
https://www.ncbi.nlm.nih.gov/pubmed/37833763
http://dx.doi.org/10.1186/s12917-023-03767-1
_version_ 1785119974154567680
author Dang, Sheng
Sui, Humujile
Zhang, Shuai
Wu, Dongxing
Chen, Zeliang
Zhai, Jingbo
Bai, Meirong
author_facet Dang, Sheng
Sui, Humujile
Zhang, Shuai
Wu, Dongxing
Chen, Zeliang
Zhai, Jingbo
Bai, Meirong
author_sort Dang, Sheng
collection PubMed
description BACKGROUND: Brucellosis is a common zoonotic disease caused by Brucella, which causes enormous economic losses and public burden to epidemic areas. Early and precise diagnosis and timely culling of infected animals are crucial to prevent the infection and spread of Brucella. In recent years, RNA-guided CRISPR/Cas12a(Clustered Regularly Interspaced Short Palindromic Repeats and its associated protein 12a) nucleases have shown great promise in nucleic acid detection. This research aims to develop a CRISPR/CAST (CRISPR/Cas12a Test strip) package that can rapidly detect Brucella nucleic acid during on-site screening, especially on remote family pastures. The CRISPR/Cas12a system combined with recombinase polymerase amplification (RPA), and lateral flow read-out. RESULTS: We selected the conserved gene bp26, which commonly used in Brucella infection detection and compared on Genbank with other Brucella species. The genomes of Brucella abortus 2308, Brucella suis S2, Brucella melitansis 16 M, and Brucella suis 1330, et al. were aligned, and the sequences were found to be consistent. Therefore, the experiments were only performed on B. melitensis. With the CRISPR/CAST package, the assay of Brucella nucleic acid can be completed within 30 min under isothermal temperature conditions, with a sensitivity of 10 copies/μl. Additionally, no antigen cross-reaction was observed against Yersinia enterocolitica O:9, Escherichia coli O157, Salmonella enterica serovar Urbana O:30, and Francisella tularensis. The serum samples of 398 sheep and 100 cattle were tested by the CRISPR/CAST package, of which 31 sheep and 8 cattle were Brucella DNA positive. The detection rate was consistent with the qPCR results and higher than that of the Rose Bengal Test (RBT, 19 sheep and 5 cattle were serum positive). CONCLUSIONS: The CRISPR/CAST package can accurately detect Brucella DNA in infected livestock within 30 min and exhibits several advantages, including simplicity, speed, high sensitivity, and strong specificity with no window period. In addition, no expensive equipment, standard laboratory, or professional operators are needed for the package. It is an effective tool for screening in the field and obtaining early, rapid diagnoses of Brucella infection. The package is an efficient tool for preventing and controlling epidemics. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12917-023-03767-1
format Online
Article
Text
id pubmed-10571365
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-105713652023-10-14 CRISPR-Cas12a test strip (CRISPR/CAST) package: In-situ detection of Brucella from infected livestock Dang, Sheng Sui, Humujile Zhang, Shuai Wu, Dongxing Chen, Zeliang Zhai, Jingbo Bai, Meirong BMC Vet Res Research BACKGROUND: Brucellosis is a common zoonotic disease caused by Brucella, which causes enormous economic losses and public burden to epidemic areas. Early and precise diagnosis and timely culling of infected animals are crucial to prevent the infection and spread of Brucella. In recent years, RNA-guided CRISPR/Cas12a(Clustered Regularly Interspaced Short Palindromic Repeats and its associated protein 12a) nucleases have shown great promise in nucleic acid detection. This research aims to develop a CRISPR/CAST (CRISPR/Cas12a Test strip) package that can rapidly detect Brucella nucleic acid during on-site screening, especially on remote family pastures. The CRISPR/Cas12a system combined with recombinase polymerase amplification (RPA), and lateral flow read-out. RESULTS: We selected the conserved gene bp26, which commonly used in Brucella infection detection and compared on Genbank with other Brucella species. The genomes of Brucella abortus 2308, Brucella suis S2, Brucella melitansis 16 M, and Brucella suis 1330, et al. were aligned, and the sequences were found to be consistent. Therefore, the experiments were only performed on B. melitensis. With the CRISPR/CAST package, the assay of Brucella nucleic acid can be completed within 30 min under isothermal temperature conditions, with a sensitivity of 10 copies/μl. Additionally, no antigen cross-reaction was observed against Yersinia enterocolitica O:9, Escherichia coli O157, Salmonella enterica serovar Urbana O:30, and Francisella tularensis. The serum samples of 398 sheep and 100 cattle were tested by the CRISPR/CAST package, of which 31 sheep and 8 cattle were Brucella DNA positive. The detection rate was consistent with the qPCR results and higher than that of the Rose Bengal Test (RBT, 19 sheep and 5 cattle were serum positive). CONCLUSIONS: The CRISPR/CAST package can accurately detect Brucella DNA in infected livestock within 30 min and exhibits several advantages, including simplicity, speed, high sensitivity, and strong specificity with no window period. In addition, no expensive equipment, standard laboratory, or professional operators are needed for the package. It is an effective tool for screening in the field and obtaining early, rapid diagnoses of Brucella infection. The package is an efficient tool for preventing and controlling epidemics. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12917-023-03767-1 BioMed Central 2023-10-13 /pmc/articles/PMC10571365/ /pubmed/37833763 http://dx.doi.org/10.1186/s12917-023-03767-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Dang, Sheng
Sui, Humujile
Zhang, Shuai
Wu, Dongxing
Chen, Zeliang
Zhai, Jingbo
Bai, Meirong
CRISPR-Cas12a test strip (CRISPR/CAST) package: In-situ detection of Brucella from infected livestock
title CRISPR-Cas12a test strip (CRISPR/CAST) package: In-situ detection of Brucella from infected livestock
title_full CRISPR-Cas12a test strip (CRISPR/CAST) package: In-situ detection of Brucella from infected livestock
title_fullStr CRISPR-Cas12a test strip (CRISPR/CAST) package: In-situ detection of Brucella from infected livestock
title_full_unstemmed CRISPR-Cas12a test strip (CRISPR/CAST) package: In-situ detection of Brucella from infected livestock
title_short CRISPR-Cas12a test strip (CRISPR/CAST) package: In-situ detection of Brucella from infected livestock
title_sort crispr-cas12a test strip (crispr/cast) package: in-situ detection of brucella from infected livestock
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10571365/
https://www.ncbi.nlm.nih.gov/pubmed/37833763
http://dx.doi.org/10.1186/s12917-023-03767-1
work_keys_str_mv AT dangsheng crisprcas12ateststripcrisprcastpackageinsitudetectionofbrucellafrominfectedlivestock
AT suihumujile crisprcas12ateststripcrisprcastpackageinsitudetectionofbrucellafrominfectedlivestock
AT zhangshuai crisprcas12ateststripcrisprcastpackageinsitudetectionofbrucellafrominfectedlivestock
AT wudongxing crisprcas12ateststripcrisprcastpackageinsitudetectionofbrucellafrominfectedlivestock
AT chenzeliang crisprcas12ateststripcrisprcastpackageinsitudetectionofbrucellafrominfectedlivestock
AT zhaijingbo crisprcas12ateststripcrisprcastpackageinsitudetectionofbrucellafrominfectedlivestock
AT baimeirong crisprcas12ateststripcrisprcastpackageinsitudetectionofbrucellafrominfectedlivestock