CRISPR-based strategies for sample-to-answer monkeypox detection: current status and emerging opportunities
The global health threat posed by the Monkeypox virus (Mpox) requires swift, simple, and accurate detection methods for effective management, emphasizing the growing necessity for decentralized point-of-care (POC) diagnostic solutions. The clustered regularly interspaced short palindromic repeats (C...
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Veröffentlicht in: | Nanotechnology 2024-11, Vol.36 (4), p.42001 |
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creator | Ahamed, Md Ahasan Politza, Anthony J Liu, Tianyi Khalid, Muhammad Asad Ullah Zhang, Huanshu Guan, Weihua |
description | The global health threat posed by the Monkeypox virus (Mpox) requires swift, simple, and accurate detection methods for effective management, emphasizing the growing necessity for decentralized point-of-care (POC) diagnostic solutions. The clustered regularly interspaced short palindromic repeats (CRISPR), initially known for its effective nucleic acid detection abilities, presents itself as an attractive diagnostic strategy. CRISPR offers exceptional sensitivity, single-base specificity, and programmability. Here, we reviewed the latest developments in CRISPR-based POC devices and testing strategies for Mpox detection. We explored the crucial role of genetic sequencing in designing crRNA for CRISPR reaction and understanding Mpox transmission and mutations. Additionally, we showed the integration of CRISPR-Cas12 strategy with pre-amplification and amplification-free methods. Our study also focused on the significant role of Cas12 proteins and the effectiveness of Cas12 coupled with recombinase polymerase amplification (RPA) for Mpox detection. We envision the future prospects and challenges, positioning CRISPR-Cas12-based POC devices as a frontrunner in the next generation of molecular biosensing technologies. |
doi_str_mv | 10.1088/1361-6528/ad892b |
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The clustered regularly interspaced short palindromic repeats (CRISPR), initially known for its effective nucleic acid detection abilities, presents itself as an attractive diagnostic strategy. CRISPR offers exceptional sensitivity, single-base specificity, and programmability. Here, we reviewed the latest developments in CRISPR-based POC devices and testing strategies for Mpox detection. We explored the crucial role of genetic sequencing in designing crRNA for CRISPR reaction and understanding Mpox transmission and mutations. Additionally, we showed the integration of CRISPR-Cas12 strategy with pre-amplification and amplification-free methods. Our study also focused on the significant role of Cas12 proteins and the effectiveness of Cas12 coupled with recombinase polymerase amplification (RPA) for Mpox detection. We envision the future prospects and challenges, positioning CRISPR-Cas12-based POC devices as a frontrunner in the next generation of molecular biosensing technologies.</description><identifier>ISSN: 0957-4484</identifier><identifier>ISSN: 1361-6528</identifier><identifier>EISSN: 1361-6528</identifier><identifier>DOI: 10.1088/1361-6528/ad892b</identifier><identifier>PMID: 39433062</identifier><identifier>CODEN: NNOTER</identifier><language>eng</language><publisher>England: IOP Publishing</publisher><subject>Biology and Medicine ; Cas12 ; Clustered Regularly Interspaced Short Palindromic Repeats - genetics ; CRISPR ; CRISPR-Cas Systems - genetics ; Humans ; monkeypox ; Monkeypox virus - genetics ; Mpox (monkeypox) - diagnosis ; nucleic acid ; point-of-care ; Point-of-Care Systems ; RPA ; Topical Review</subject><ispartof>Nanotechnology, 2024-11, Vol.36 (4), p.42001</ispartof><rights>2024 The Author(s). Published by IOP Publishing Ltd</rights><rights>Creative Commons Attribution license.</rights><rights>2024 The Author(s). Published by IOP Publishing Ltd 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c275t-be3ba16f30e323f7db02c4faf75f60f6d3095a409a6b4d5f3970bc492e99788e3</cites><orcidid>0009-0009-8332-7298 ; 0009-0006-9962-2994 ; 0009-0007-8084-4690 ; 0000-0002-8435-9672 ; 0009-0005-8670-2357 ; 0000-0001-5926-1764</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://iopscience.iop.org/article/10.1088/1361-6528/ad892b/pdf$$EPDF$$P50$$Giop$$Hfree_for_read</linktopdf><link.rule.ids>230,314,780,784,885,27924,27925,53846,53893</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39433062$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ahamed, Md Ahasan</creatorcontrib><creatorcontrib>Politza, Anthony J</creatorcontrib><creatorcontrib>Liu, Tianyi</creatorcontrib><creatorcontrib>Khalid, Muhammad Asad Ullah</creatorcontrib><creatorcontrib>Zhang, Huanshu</creatorcontrib><creatorcontrib>Guan, Weihua</creatorcontrib><title>CRISPR-based strategies for sample-to-answer monkeypox detection: current status and emerging opportunities</title><title>Nanotechnology</title><addtitle>Nano</addtitle><addtitle>Nanotechnology</addtitle><description>The global health threat posed by the Monkeypox virus (Mpox) requires swift, simple, and accurate detection methods for effective management, emphasizing the growing necessity for decentralized point-of-care (POC) diagnostic solutions. The clustered regularly interspaced short palindromic repeats (CRISPR), initially known for its effective nucleic acid detection abilities, presents itself as an attractive diagnostic strategy. CRISPR offers exceptional sensitivity, single-base specificity, and programmability. Here, we reviewed the latest developments in CRISPR-based POC devices and testing strategies for Mpox detection. We explored the crucial role of genetic sequencing in designing crRNA for CRISPR reaction and understanding Mpox transmission and mutations. Additionally, we showed the integration of CRISPR-Cas12 strategy with pre-amplification and amplification-free methods. Our study also focused on the significant role of Cas12 proteins and the effectiveness of Cas12 coupled with recombinase polymerase amplification (RPA) for Mpox detection. We envision the future prospects and challenges, positioning CRISPR-Cas12-based POC devices as a frontrunner in the next generation of molecular biosensing technologies.</description><subject>Biology and Medicine</subject><subject>Cas12</subject><subject>Clustered Regularly Interspaced Short Palindromic Repeats - genetics</subject><subject>CRISPR</subject><subject>CRISPR-Cas Systems - genetics</subject><subject>Humans</subject><subject>monkeypox</subject><subject>Monkeypox virus - genetics</subject><subject>Mpox (monkeypox) - diagnosis</subject><subject>nucleic acid</subject><subject>point-of-care</subject><subject>Point-of-Care Systems</subject><subject>RPA</subject><subject>Topical Review</subject><issn>0957-4484</issn><issn>1361-6528</issn><issn>1361-6528</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>O3W</sourceid><sourceid>EIF</sourceid><recordid>eNp1kc1P2zAYhy3EBF3HfSfkIwcy_JEPmwtCFWyVKm1i42w5yevOkNjBdhj975eqrBoHTpbs3-_xaz8IfabkCyVCXFBe0qwsmLjQrZCsPkCz_dYhmhFZVFmei_wYfYzxgRBKBaNH6JjLnHNSshl6XNwtf_64y2odocUxBZ1gbSFi4wOOuh86yJLPtIt_IODeu0fYDP4Ft5CgSda7S9yMIYBLU1mnMWLtWgw9hLV1a-yHwYc0Opsm5if0weguwsnrOkf3tze_Ft-y1fevy8X1KmtYVaSsBl5rWhpOgDNuqrYmrMmNNlVhSmLKlk_v0jmRuqzztjBcVqRucslAykoI4HN0teMOY91D20zDBd2pIdheh43y2qq3J87-Vmv_rCgtOBeCTYSzV0LwTyPEpHobG-g67cCPUXFKJRVSFtso2UWb4GMMYPb3UKK2ktTWiNoaUTtJU-X0__n2hX9WpsD5LmD9oB78GNz0Xe_z_gJIKJ6c</recordid><startdate>20241104</startdate><enddate>20241104</enddate><creator>Ahamed, Md Ahasan</creator><creator>Politza, Anthony J</creator><creator>Liu, Tianyi</creator><creator>Khalid, Muhammad Asad Ullah</creator><creator>Zhang, Huanshu</creator><creator>Guan, Weihua</creator><general>IOP Publishing</general><scope>O3W</scope><scope>TSCCA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0009-0009-8332-7298</orcidid><orcidid>https://orcid.org/0009-0006-9962-2994</orcidid><orcidid>https://orcid.org/0009-0007-8084-4690</orcidid><orcidid>https://orcid.org/0000-0002-8435-9672</orcidid><orcidid>https://orcid.org/0009-0005-8670-2357</orcidid><orcidid>https://orcid.org/0000-0001-5926-1764</orcidid></search><sort><creationdate>20241104</creationdate><title>CRISPR-based strategies for sample-to-answer monkeypox detection: current status and emerging opportunities</title><author>Ahamed, Md Ahasan ; 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subjects | Biology and Medicine Cas12 Clustered Regularly Interspaced Short Palindromic Repeats - genetics CRISPR CRISPR-Cas Systems - genetics Humans monkeypox Monkeypox virus - genetics Mpox (monkeypox) - diagnosis nucleic acid point-of-care Point-of-Care Systems RPA Topical Review |
title | CRISPR-based strategies for sample-to-answer monkeypox detection: current status and emerging opportunities |
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