Single- and Two-Stage, Closed-Tube, Point-of-Care, Molecular Detection of SARS-CoV‑2
Short of a vaccine, frequent and rapid testing, preferably at home, is the most effective strategy to contain the COVID-19 pandemic. Herein, we report on single-stage and two-stage molecular diagnostic tests that can be carried out with simple or no instrumentation. Our single-stage amplification is...
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Veröffentlicht in: | Analytical chemistry (Washington) 2021-09, Vol.93 (38), p.13063-13071 |
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creator | Song, Jinzhao El-Tholoth, Mohamed Li, Yize Graham-Wooten, Jevon Liang, Yining Li, Juan Li, Weijian Weiss, Susan R Collman, Ronald G Bau, Haim H |
description | Short of a vaccine, frequent and rapid testing, preferably at home, is the most effective strategy to contain the COVID-19 pandemic. Herein, we report on single-stage and two-stage molecular diagnostic tests that can be carried out with simple or no instrumentation. Our single-stage amplification is reverse transcription-loop mediated isothermal amplification (RT-LAMP) with custom-designed primers targeting the ORF1ab and the N gene regions of the virus genome. Our new two-stage amplification, dubbed Penn-RAMP, comprises recombinase isothermal amplification (RT-RPA) as its first stage and LAMP as its second stage. We compared various sample preparation strategies aimed at deactivating the virus while preserving its RNA and tested contrived and patient samples, consisting of nasopharyngeal swabs, oropharyngeal swabs, and saliva. Amplicons were detected either in real time with fluorescent intercalating dye or after amplification with the intercalating colorimetric dye LCV, which is insensitive to sample’s PH. Our single RT-LAMP tests can be carried out instrumentation-free. To enable concurrent testing of multiple samples, we developed an inexpensive heat block that supports both the single-stage and two-stage amplification. Our RT-LAMP and Penn-RAMP assays have, respectively, analytical sensitivities of 50 and 5 virions/reaction. Both our single- and two-stage assays have successfully detected SARS-CoV-2 in patients with viral loads corresponding to the reverse transcription-quantitative polymerase chain reaction (RT-qPCR) threshold cycle smaller than 32 while operating with minimally processed samples, without nucleic acid isolation. Penn-RAMP provides a 10-fold better sensitivity than RT-LAMP and does not need thermal cycling like PCR assays. All reagents are amenable to dry, refrigeration-free storage. The SARS-CoV-2 test described herein is suitable for screening at home, at the point of need, and in resource-poor settings. |
doi_str_mv | 10.1021/acs.analchem.1c03016 |
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Herein, we report on single-stage and two-stage molecular diagnostic tests that can be carried out with simple or no instrumentation. Our single-stage amplification is reverse transcription-loop mediated isothermal amplification (RT-LAMP) with custom-designed primers targeting the ORF1ab and the N gene regions of the virus genome. Our new two-stage amplification, dubbed Penn-RAMP, comprises recombinase isothermal amplification (RT-RPA) as its first stage and LAMP as its second stage. We compared various sample preparation strategies aimed at deactivating the virus while preserving its RNA and tested contrived and patient samples, consisting of nasopharyngeal swabs, oropharyngeal swabs, and saliva. Amplicons were detected either in real time with fluorescent intercalating dye or after amplification with the intercalating colorimetric dye LCV, which is insensitive to sample’s PH. Our single RT-LAMP tests can be carried out instrumentation-free. To enable concurrent testing of multiple samples, we developed an inexpensive heat block that supports both the single-stage and two-stage amplification. Our RT-LAMP and Penn-RAMP assays have, respectively, analytical sensitivities of 50 and 5 virions/reaction. Both our single- and two-stage assays have successfully detected SARS-CoV-2 in patients with viral loads corresponding to the reverse transcription-quantitative polymerase chain reaction (RT-qPCR) threshold cycle smaller than 32 while operating with minimally processed samples, without nucleic acid isolation. Penn-RAMP provides a 10-fold better sensitivity than RT-LAMP and does not need thermal cycling like PCR assays. All reagents are amenable to dry, refrigeration-free storage. The SARS-CoV-2 test described herein is suitable for screening at home, at the point of need, and in resource-poor settings.</description><identifier>ISSN: 0003-2700</identifier><identifier>EISSN: 1520-6882</identifier><identifier>DOI: 10.1021/acs.analchem.1c03016</identifier><identifier>PMID: 34541844</identifier><language>eng</language><publisher>Washington: American Chemical Society</publisher><subject>Assaying ; Chemistry ; Colorimetry ; COVID-19 ; Dyes ; Fluorescence ; Genomes ; Instrumentation ; Instruments ; N gene ; Nucleic acids ; Pandemics ; Polymerase chain reaction ; Reagents ; Recombinase ; Refrigeration ; Reverse transcription ; RNA viruses ; Saliva ; Sample preparation ; Sensitivity analysis ; Severe acute respiratory syndrome ; Severe acute respiratory syndrome coronavirus 2 ; Thermal cycling ; Vaccines ; Viral diseases ; Virions ; Viruses</subject><ispartof>Analytical chemistry (Washington), 2021-09, Vol.93 (38), p.13063-13071</ispartof><rights>2021 American Chemical Society</rights><rights>Copyright American Chemical Society Sep 28, 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a454t-adae3452c564d922a970d55fa8aea82334e2ba28f3fe41e60f50fdf87675f2f73</citedby><cites>FETCH-LOGICAL-a454t-adae3452c564d922a970d55fa8aea82334e2ba28f3fe41e60f50fdf87675f2f73</cites><orcidid>0000-0002-5253-5168 ; 0000-0002-2097-8685</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.analchem.1c03016$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.analchem.1c03016$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,776,780,881,2752,27053,27901,27902,56713,56763</link.rule.ids></links><search><creatorcontrib>Song, Jinzhao</creatorcontrib><creatorcontrib>El-Tholoth, Mohamed</creatorcontrib><creatorcontrib>Li, Yize</creatorcontrib><creatorcontrib>Graham-Wooten, Jevon</creatorcontrib><creatorcontrib>Liang, Yining</creatorcontrib><creatorcontrib>Li, Juan</creatorcontrib><creatorcontrib>Li, Weijian</creatorcontrib><creatorcontrib>Weiss, Susan R</creatorcontrib><creatorcontrib>Collman, Ronald G</creatorcontrib><creatorcontrib>Bau, Haim H</creatorcontrib><title>Single- and Two-Stage, Closed-Tube, Point-of-Care, Molecular Detection of SARS-CoV‑2</title><title>Analytical chemistry (Washington)</title><addtitle>Anal. Chem</addtitle><description>Short of a vaccine, frequent and rapid testing, preferably at home, is the most effective strategy to contain the COVID-19 pandemic. Herein, we report on single-stage and two-stage molecular diagnostic tests that can be carried out with simple or no instrumentation. Our single-stage amplification is reverse transcription-loop mediated isothermal amplification (RT-LAMP) with custom-designed primers targeting the ORF1ab and the N gene regions of the virus genome. Our new two-stage amplification, dubbed Penn-RAMP, comprises recombinase isothermal amplification (RT-RPA) as its first stage and LAMP as its second stage. We compared various sample preparation strategies aimed at deactivating the virus while preserving its RNA and tested contrived and patient samples, consisting of nasopharyngeal swabs, oropharyngeal swabs, and saliva. Amplicons were detected either in real time with fluorescent intercalating dye or after amplification with the intercalating colorimetric dye LCV, which is insensitive to sample’s PH. Our single RT-LAMP tests can be carried out instrumentation-free. To enable concurrent testing of multiple samples, we developed an inexpensive heat block that supports both the single-stage and two-stage amplification. Our RT-LAMP and Penn-RAMP assays have, respectively, analytical sensitivities of 50 and 5 virions/reaction. Both our single- and two-stage assays have successfully detected SARS-CoV-2 in patients with viral loads corresponding to the reverse transcription-quantitative polymerase chain reaction (RT-qPCR) threshold cycle smaller than 32 while operating with minimally processed samples, without nucleic acid isolation. Penn-RAMP provides a 10-fold better sensitivity than RT-LAMP and does not need thermal cycling like PCR assays. All reagents are amenable to dry, refrigeration-free storage. The SARS-CoV-2 test described herein is suitable for screening at home, at the point of need, and in resource-poor settings.</description><subject>Assaying</subject><subject>Chemistry</subject><subject>Colorimetry</subject><subject>COVID-19</subject><subject>Dyes</subject><subject>Fluorescence</subject><subject>Genomes</subject><subject>Instrumentation</subject><subject>Instruments</subject><subject>N gene</subject><subject>Nucleic acids</subject><subject>Pandemics</subject><subject>Polymerase chain reaction</subject><subject>Reagents</subject><subject>Recombinase</subject><subject>Refrigeration</subject><subject>Reverse transcription</subject><subject>RNA viruses</subject><subject>Saliva</subject><subject>Sample preparation</subject><subject>Sensitivity analysis</subject><subject>Severe acute respiratory syndrome</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Thermal cycling</subject><subject>Vaccines</subject><subject>Viral diseases</subject><subject>Virions</subject><subject>Viruses</subject><issn>0003-2700</issn><issn>1520-6882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kc1uFDEQhC0EIkvgDTiMxIUDXtoez9i5IEXDrxQEYpdcrV5PezORd5zYMyBuvAKvyJPgsEskOHBqlfqrUknF2GMBSwFSPEeXlzhicBe0WwoHNYj2DluIRgJvjZF32QIAai41wBF7kPMlgBAFus-OatUoYZRasPPVMG4D8QrHvlp_jXw14ZaeVV2ImXq-njdFfIzDOPHoeYepyPcxkJsDpuolTeSmIY5V9NXq9NOKd_H85_cf8iG75zFkenS4x-zz61fr7i0_-_DmXXd6xrE0mDj2SKWLdE2r-hMp8URD3zQeDRIaWdeK5Aal8bUnJagF34DvvdGtbrz0uj5mL_a5V_NmR72jcUoY7FUadpi-2YiD_fszDhd2G79Yo0q8MCXg6SEgxeuZ8mR3Q3YUAo4U52xlo5VWUtdQ0Cf_oJdxTmWB35TWxmghC6X2lEsx50T-towAezOcLcPZP8PZw3DFBnvbzfc297-WXx0qnTM</recordid><startdate>20210928</startdate><enddate>20210928</enddate><creator>Song, Jinzhao</creator><creator>El-Tholoth, Mohamed</creator><creator>Li, Yize</creator><creator>Graham-Wooten, Jevon</creator><creator>Liang, Yining</creator><creator>Li, Juan</creator><creator>Li, Weijian</creator><creator>Weiss, Susan R</creator><creator>Collman, Ronald G</creator><creator>Bau, Haim H</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7TM</scope><scope>7U5</scope><scope>7U7</scope><scope>7U9</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5253-5168</orcidid><orcidid>https://orcid.org/0000-0002-2097-8685</orcidid></search><sort><creationdate>20210928</creationdate><title>Single- and Two-Stage, Closed-Tube, Point-of-Care, Molecular Detection of SARS-CoV‑2</title><author>Song, Jinzhao ; El-Tholoth, Mohamed ; Li, Yize ; Graham-Wooten, Jevon ; Liang, Yining ; Li, Juan ; Li, Weijian ; Weiss, Susan R ; Collman, Ronald G ; Bau, Haim H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a454t-adae3452c564d922a970d55fa8aea82334e2ba28f3fe41e60f50fdf87675f2f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Assaying</topic><topic>Chemistry</topic><topic>Colorimetry</topic><topic>COVID-19</topic><topic>Dyes</topic><topic>Fluorescence</topic><topic>Genomes</topic><topic>Instrumentation</topic><topic>Instruments</topic><topic>N gene</topic><topic>Nucleic acids</topic><topic>Pandemics</topic><topic>Polymerase chain reaction</topic><topic>Reagents</topic><topic>Recombinase</topic><topic>Refrigeration</topic><topic>Reverse transcription</topic><topic>RNA viruses</topic><topic>Saliva</topic><topic>Sample preparation</topic><topic>Sensitivity analysis</topic><topic>Severe acute respiratory syndrome</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Thermal cycling</topic><topic>Vaccines</topic><topic>Viral diseases</topic><topic>Virions</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Song, Jinzhao</creatorcontrib><creatorcontrib>El-Tholoth, Mohamed</creatorcontrib><creatorcontrib>Li, Yize</creatorcontrib><creatorcontrib>Graham-Wooten, Jevon</creatorcontrib><creatorcontrib>Liang, Yining</creatorcontrib><creatorcontrib>Li, Juan</creatorcontrib><creatorcontrib>Li, Weijian</creatorcontrib><creatorcontrib>Weiss, Susan R</creatorcontrib><creatorcontrib>Collman, Ronald G</creatorcontrib><creatorcontrib>Bau, Haim H</creatorcontrib><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Analytical chemistry (Washington)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Song, Jinzhao</au><au>El-Tholoth, Mohamed</au><au>Li, Yize</au><au>Graham-Wooten, Jevon</au><au>Liang, Yining</au><au>Li, Juan</au><au>Li, Weijian</au><au>Weiss, Susan R</au><au>Collman, Ronald G</au><au>Bau, Haim H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Single- and Two-Stage, Closed-Tube, Point-of-Care, Molecular Detection of SARS-CoV‑2</atitle><jtitle>Analytical chemistry (Washington)</jtitle><addtitle>Anal. Chem</addtitle><date>2021-09-28</date><risdate>2021</risdate><volume>93</volume><issue>38</issue><spage>13063</spage><epage>13071</epage><pages>13063-13071</pages><issn>0003-2700</issn><eissn>1520-6882</eissn><abstract>Short of a vaccine, frequent and rapid testing, preferably at home, is the most effective strategy to contain the COVID-19 pandemic. Herein, we report on single-stage and two-stage molecular diagnostic tests that can be carried out with simple or no instrumentation. Our single-stage amplification is reverse transcription-loop mediated isothermal amplification (RT-LAMP) with custom-designed primers targeting the ORF1ab and the N gene regions of the virus genome. Our new two-stage amplification, dubbed Penn-RAMP, comprises recombinase isothermal amplification (RT-RPA) as its first stage and LAMP as its second stage. We compared various sample preparation strategies aimed at deactivating the virus while preserving its RNA and tested contrived and patient samples, consisting of nasopharyngeal swabs, oropharyngeal swabs, and saliva. Amplicons were detected either in real time with fluorescent intercalating dye or after amplification with the intercalating colorimetric dye LCV, which is insensitive to sample’s PH. Our single RT-LAMP tests can be carried out instrumentation-free. To enable concurrent testing of multiple samples, we developed an inexpensive heat block that supports both the single-stage and two-stage amplification. Our RT-LAMP and Penn-RAMP assays have, respectively, analytical sensitivities of 50 and 5 virions/reaction. Both our single- and two-stage assays have successfully detected SARS-CoV-2 in patients with viral loads corresponding to the reverse transcription-quantitative polymerase chain reaction (RT-qPCR) threshold cycle smaller than 32 while operating with minimally processed samples, without nucleic acid isolation. Penn-RAMP provides a 10-fold better sensitivity than RT-LAMP and does not need thermal cycling like PCR assays. All reagents are amenable to dry, refrigeration-free storage. The SARS-CoV-2 test described herein is suitable for screening at home, at the point of need, and in resource-poor settings.</abstract><cop>Washington</cop><pub>American Chemical Society</pub><pmid>34541844</pmid><doi>10.1021/acs.analchem.1c03016</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-5253-5168</orcidid><orcidid>https://orcid.org/0000-0002-2097-8685</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Assaying Chemistry Colorimetry COVID-19 Dyes Fluorescence Genomes Instrumentation Instruments N gene Nucleic acids Pandemics Polymerase chain reaction Reagents Recombinase Refrigeration Reverse transcription RNA viruses Saliva Sample preparation Sensitivity analysis Severe acute respiratory syndrome Severe acute respiratory syndrome coronavirus 2 Thermal cycling Vaccines Viral diseases Virions Viruses |
title | Single- and Two-Stage, Closed-Tube, Point-of-Care, Molecular Detection of SARS-CoV‑2 |
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