Loading…
Lateral flow biosensor based on LAMP-CRISPR/Cas12a for sensitive and visualized detection of Salmonella spp
Salmonella is a major pathogen that causes serious foodborne diseases in humans and poses a serious threat to food safety and public health worldwide. Its rapid and accurate diagnosis is essential to prevent bacterial contamination of food. This study aimed to develop a lateral flow biosensor (LFB)...
Saved in:
Published in: | Food control 2023-03, Vol.145, p.109494, Article 109494 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c312t-26a676e22319ab40a6b6ee6b5067055e4bf0d079d8b4eea537a3ec4578b3de53 |
---|---|
cites | cdi_FETCH-LOGICAL-c312t-26a676e22319ab40a6b6ee6b5067055e4bf0d079d8b4eea537a3ec4578b3de53 |
container_end_page | |
container_issue | |
container_start_page | 109494 |
container_title | Food control |
container_volume | 145 |
creator | Lee, So-Young Oh, Se-Wook |
description | Salmonella is a major pathogen that causes serious foodborne diseases in humans and poses a serious threat to food safety and public health worldwide. Its rapid and accurate diagnosis is essential to prevent bacterial contamination of food. This study aimed to develop a lateral flow biosensor (LFB) based on loop-mediated isothermal amplification (LAMP)-clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR associated protein 12a (Cas12a) that is affordable and can aid in visually detecting Salmonella in a food sample. False positives were prevented by synthesizing CRISPR ribonucleic acid (crRNA) with a selected 21-base pair protospacer that did not overlap with the used LAMP primers. A single-stranded deoxyribonucleic acid (DNA) probe labeled with biotin and 6-Carboxyfluorescein (6-FAM) was used for designing the LFB. The duration of these processes was as follows: DNA extraction (20 min), LAMP (60 min), Cas12a cleavage (5 min), and LFB (5 min). The detection limit was 1.22 × 10° CFU/mL in pure culture. The validity of the LAMP-CRISPR/Cas12a based LFB was verified by detecting Salmonella in onions, melon, and salami. Consequently, the developed LAMP-CRISPR/Cas12a based LFB assay show the potential for rapid on-site detection of Salmonella with high specificity, sensitivity, convenience, mobility, low cost, and affordability.
•LFB based on LAMP-CRISPR/Cas12a was developed for detection of Salmonella.•The developed method demonstrated suitability for naked-eye detection of Salmonella.•The detection can be completed within 100 min for on-site detection. |
doi_str_mv | 10.1016/j.foodcont.2022.109494 |
format | article |
fullrecord | <record><control><sourceid>elsevier_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1016_j_foodcont_2022_109494</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0956713522006879</els_id><sourcerecordid>S0956713522006879</sourcerecordid><originalsourceid>FETCH-LOGICAL-c312t-26a676e22319ab40a6b6ee6b5067055e4bf0d079d8b4eea537a3ec4578b3de53</originalsourceid><addsrcrecordid>eNqFkNtKAzEQQIMoWKu_IPmBbXPZJN03S_FSWLG0fQ_JZhZSt5uSrBX9elOqzz7NMDNnmDkI3VMyoYTK6W7ShuCa0A8TRhjLxaqsygs0ojPFC0VZdYlGpBIy51xco5uUdoRQRSgZoffaDBBNh9sufGLrQ4I-hYitSeBw6HE9f10Vi_Vys1pPFyZRZnCb-6cxP_gjYNM7fPTpw3T-OyMOBmgGn8nQ4o3p9qGHrjM4HQ636Ko1XYK73zhG26fH7eKlqN-el4t5XTScsqFg0kglgTFOK2NLYqSVANIKIhURAkrbEkdU5Wa2BDCCK8OhKYWaWe5A8DGS57VNDClFaPUh-r2JX5oSfTKmd_rPmD4Z02djGXw4g5CPO3qIOjUe-gacj_kn7YL_b8UPUIF4ww</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Lateral flow biosensor based on LAMP-CRISPR/Cas12a for sensitive and visualized detection of Salmonella spp</title><source>ScienceDirect Freedom Collection 2022-2024</source><creator>Lee, So-Young ; Oh, Se-Wook</creator><creatorcontrib>Lee, So-Young ; Oh, Se-Wook</creatorcontrib><description>Salmonella is a major pathogen that causes serious foodborne diseases in humans and poses a serious threat to food safety and public health worldwide. Its rapid and accurate diagnosis is essential to prevent bacterial contamination of food. This study aimed to develop a lateral flow biosensor (LFB) based on loop-mediated isothermal amplification (LAMP)-clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR associated protein 12a (Cas12a) that is affordable and can aid in visually detecting Salmonella in a food sample. False positives were prevented by synthesizing CRISPR ribonucleic acid (crRNA) with a selected 21-base pair protospacer that did not overlap with the used LAMP primers. A single-stranded deoxyribonucleic acid (DNA) probe labeled with biotin and 6-Carboxyfluorescein (6-FAM) was used for designing the LFB. The duration of these processes was as follows: DNA extraction (20 min), LAMP (60 min), Cas12a cleavage (5 min), and LFB (5 min). The detection limit was 1.22 × 10° CFU/mL in pure culture. The validity of the LAMP-CRISPR/Cas12a based LFB was verified by detecting Salmonella in onions, melon, and salami. Consequently, the developed LAMP-CRISPR/Cas12a based LFB assay show the potential for rapid on-site detection of Salmonella with high specificity, sensitivity, convenience, mobility, low cost, and affordability.
•LFB based on LAMP-CRISPR/Cas12a was developed for detection of Salmonella.•The developed method demonstrated suitability for naked-eye detection of Salmonella.•The detection can be completed within 100 min for on-site detection.</description><identifier>ISSN: 0956-7135</identifier><identifier>EISSN: 1873-7129</identifier><identifier>DOI: 10.1016/j.foodcont.2022.109494</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Clustered regularly interspaced short palindromic repeats (CRISPR)/ CRISPR associated Protein 12a ; Lateral flow biosensor ; Loop-mediated isothermal amplification ; Rapid detection ; Salmonella</subject><ispartof>Food control, 2023-03, Vol.145, p.109494, Article 109494</ispartof><rights>2022 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c312t-26a676e22319ab40a6b6ee6b5067055e4bf0d079d8b4eea537a3ec4578b3de53</citedby><cites>FETCH-LOGICAL-c312t-26a676e22319ab40a6b6ee6b5067055e4bf0d079d8b4eea537a3ec4578b3de53</cites><orcidid>0000-0002-8580-6032</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Lee, So-Young</creatorcontrib><creatorcontrib>Oh, Se-Wook</creatorcontrib><title>Lateral flow biosensor based on LAMP-CRISPR/Cas12a for sensitive and visualized detection of Salmonella spp</title><title>Food control</title><description>Salmonella is a major pathogen that causes serious foodborne diseases in humans and poses a serious threat to food safety and public health worldwide. Its rapid and accurate diagnosis is essential to prevent bacterial contamination of food. This study aimed to develop a lateral flow biosensor (LFB) based on loop-mediated isothermal amplification (LAMP)-clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR associated protein 12a (Cas12a) that is affordable and can aid in visually detecting Salmonella in a food sample. False positives were prevented by synthesizing CRISPR ribonucleic acid (crRNA) with a selected 21-base pair protospacer that did not overlap with the used LAMP primers. A single-stranded deoxyribonucleic acid (DNA) probe labeled with biotin and 6-Carboxyfluorescein (6-FAM) was used for designing the LFB. The duration of these processes was as follows: DNA extraction (20 min), LAMP (60 min), Cas12a cleavage (5 min), and LFB (5 min). The detection limit was 1.22 × 10° CFU/mL in pure culture. The validity of the LAMP-CRISPR/Cas12a based LFB was verified by detecting Salmonella in onions, melon, and salami. Consequently, the developed LAMP-CRISPR/Cas12a based LFB assay show the potential for rapid on-site detection of Salmonella with high specificity, sensitivity, convenience, mobility, low cost, and affordability.
•LFB based on LAMP-CRISPR/Cas12a was developed for detection of Salmonella.•The developed method demonstrated suitability for naked-eye detection of Salmonella.•The detection can be completed within 100 min for on-site detection.</description><subject>Clustered regularly interspaced short palindromic repeats (CRISPR)/ CRISPR associated Protein 12a</subject><subject>Lateral flow biosensor</subject><subject>Loop-mediated isothermal amplification</subject><subject>Rapid detection</subject><subject>Salmonella</subject><issn>0956-7135</issn><issn>1873-7129</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFkNtKAzEQQIMoWKu_IPmBbXPZJN03S_FSWLG0fQ_JZhZSt5uSrBX9elOqzz7NMDNnmDkI3VMyoYTK6W7ShuCa0A8TRhjLxaqsygs0ojPFC0VZdYlGpBIy51xco5uUdoRQRSgZoffaDBBNh9sufGLrQ4I-hYitSeBw6HE9f10Vi_Vys1pPFyZRZnCb-6cxP_gjYNM7fPTpw3T-OyMOBmgGn8nQ4o3p9qGHrjM4HQ636Ko1XYK73zhG26fH7eKlqN-el4t5XTScsqFg0kglgTFOK2NLYqSVANIKIhURAkrbEkdU5Wa2BDCCK8OhKYWaWe5A8DGS57VNDClFaPUh-r2JX5oSfTKmd_rPmD4Z02djGXw4g5CPO3qIOjUe-gacj_kn7YL_b8UPUIF4ww</recordid><startdate>202303</startdate><enddate>202303</enddate><creator>Lee, So-Young</creator><creator>Oh, Se-Wook</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-8580-6032</orcidid></search><sort><creationdate>202303</creationdate><title>Lateral flow biosensor based on LAMP-CRISPR/Cas12a for sensitive and visualized detection of Salmonella spp</title><author>Lee, So-Young ; Oh, Se-Wook</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c312t-26a676e22319ab40a6b6ee6b5067055e4bf0d079d8b4eea537a3ec4578b3de53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Clustered regularly interspaced short palindromic repeats (CRISPR)/ CRISPR associated Protein 12a</topic><topic>Lateral flow biosensor</topic><topic>Loop-mediated isothermal amplification</topic><topic>Rapid detection</topic><topic>Salmonella</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, So-Young</creatorcontrib><creatorcontrib>Oh, Se-Wook</creatorcontrib><collection>CrossRef</collection><jtitle>Food control</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, So-Young</au><au>Oh, Se-Wook</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lateral flow biosensor based on LAMP-CRISPR/Cas12a for sensitive and visualized detection of Salmonella spp</atitle><jtitle>Food control</jtitle><date>2023-03</date><risdate>2023</risdate><volume>145</volume><spage>109494</spage><pages>109494-</pages><artnum>109494</artnum><issn>0956-7135</issn><eissn>1873-7129</eissn><abstract>Salmonella is a major pathogen that causes serious foodborne diseases in humans and poses a serious threat to food safety and public health worldwide. Its rapid and accurate diagnosis is essential to prevent bacterial contamination of food. This study aimed to develop a lateral flow biosensor (LFB) based on loop-mediated isothermal amplification (LAMP)-clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR associated protein 12a (Cas12a) that is affordable and can aid in visually detecting Salmonella in a food sample. False positives were prevented by synthesizing CRISPR ribonucleic acid (crRNA) with a selected 21-base pair protospacer that did not overlap with the used LAMP primers. A single-stranded deoxyribonucleic acid (DNA) probe labeled with biotin and 6-Carboxyfluorescein (6-FAM) was used for designing the LFB. The duration of these processes was as follows: DNA extraction (20 min), LAMP (60 min), Cas12a cleavage (5 min), and LFB (5 min). The detection limit was 1.22 × 10° CFU/mL in pure culture. The validity of the LAMP-CRISPR/Cas12a based LFB was verified by detecting Salmonella in onions, melon, and salami. Consequently, the developed LAMP-CRISPR/Cas12a based LFB assay show the potential for rapid on-site detection of Salmonella with high specificity, sensitivity, convenience, mobility, low cost, and affordability.
•LFB based on LAMP-CRISPR/Cas12a was developed for detection of Salmonella.•The developed method demonstrated suitability for naked-eye detection of Salmonella.•The detection can be completed within 100 min for on-site detection.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.foodcont.2022.109494</doi><orcidid>https://orcid.org/0000-0002-8580-6032</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0956-7135 |
ispartof | Food control, 2023-03, Vol.145, p.109494, Article 109494 |
issn | 0956-7135 1873-7129 |
language | eng |
recordid | cdi_crossref_primary_10_1016_j_foodcont_2022_109494 |
source | ScienceDirect Freedom Collection 2022-2024 |
subjects | Clustered regularly interspaced short palindromic repeats (CRISPR)/ CRISPR associated Protein 12a Lateral flow biosensor Loop-mediated isothermal amplification Rapid detection Salmonella |
title | Lateral flow biosensor based on LAMP-CRISPR/Cas12a for sensitive and visualized detection of Salmonella spp |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T23%3A43%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Lateral%20flow%20biosensor%20based%20on%20LAMP-CRISPR/Cas12a%20for%20sensitive%20and%20visualized%20detection%20of%20Salmonella%20spp&rft.jtitle=Food%20control&rft.au=Lee,%20So-Young&rft.date=2023-03&rft.volume=145&rft.spage=109494&rft.pages=109494-&rft.artnum=109494&rft.issn=0956-7135&rft.eissn=1873-7129&rft_id=info:doi/10.1016/j.foodcont.2022.109494&rft_dat=%3Celsevier_cross%3ES0956713522006879%3C/elsevier_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c312t-26a676e22319ab40a6b6ee6b5067055e4bf0d079d8b4eea537a3ec4578b3de53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |