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1000 Titel
  • Rapid point-of-care detection of SARS-CoV-2 using reverse transcription loop-mediated isothermal amplification (RT-LAMP)
1000 Autor/in
  1. Mautner, Lena |
  2. Baillie, Christin-Kirsty |
  3. Herold, Heike Marie |
  4. Volkwein, Wolfram |
  5. Guertler, Patrick |
  6. Eberle, Ute |
  7. Ackermann, Nikolaus |
  8. Sing, Andreas |
  9. Pavlovic, Melanie |
  10. Goerlich, Ottmar |
  11. Busch, Ulrich |
  12. Wassill, Lars |
  13. Huber, Ingrid |
  14. Baiker, Armin |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-10-21
1000 Erschienen in
1000 Quellenangabe
  • 17(1):160
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s12985-020-01435-6 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576985/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • BACKGROUND: Fast, reliable and easy to handle methods are required to facilitate urgently needed point-of-care testing (POCT) in the current coronavirus pandemic. Life-threatening severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has rapidly spread all over the world, infecting more than 33,500,000 people and killing over 1 million of them as of October 2020. Infected individuals without any symptoms might still transfer the virus to others underlining the extraordinary transmissibility of this new coronavirus. In order to identify early infections effectively, treat patients on time and control disease spreading, rapid, accurate and onsite testing methods are urgently required. RESULTS: Here we report the development of a loop-mediated isothermal amplification (LAMP) based method to detect SARS-CoV-2 genes ORF8 and N directly from pharyngeal swab samples. The established reverse transcription LAMP (RT-LAMP) assay detects SARS-CoV-2 directly from pharyngeal swab samples without previous time-consuming and laborious RNA extraction. The assay is sensitive and highly specific for SARS-CoV-2 detection, showing no cross reactivity when tested on 20 other respiratory pathogens. The assay is 12 times faster and 10 times cheaper than routine reverse transcription real-time polymerase chain reaction, depending on the assay used. CONCLUSION: The fast and easy to handle RT-LAMP assay amplifying specifically the genomic regions ORF8 and N of SARS-CoV-2 is ideally suited for POCT at e.g. railway stations, airports or hospitals. Given the current pandemic situation, rapid, cost efficient and onsite methods like the here presented RT-LAMP assay are urgently needed to contain the viral spread.
1000 Sacherschließung
gnd 1206347392 COVID-19
lokal Chlorocebus aethiops [MeSH]
lokal Molecular Diagnostic Techniques [MeSH]
lokal Clinical Virology
lokal No RNA extraction
lokal Methodology
lokal Pneumonia, Viral/virology [MeSH]
lokal Vero Cells [MeSH]
lokal Point-of-care testing
lokal SARS-CoV-2
lokal Gene N
lokal Point-of-Care Systems [MeSH]
lokal Coronavirus Infections/diagnosis [MeSH]
lokal Betacoronavirus/genetics [MeSH]
lokal Humans [MeSH]
lokal RNA, Viral/genetics [MeSH]
lokal RT-LAMP
lokal COVID-19
lokal Animals [MeSH]
lokal Betacoronavirus/isolation
lokal Rapid testing
lokal Pandemics [MeSH]
lokal Coronavirus Infections/virology [MeSH]
lokal ORF8
lokal Pneumonia, Viral/diagnosis [MeSH]
lokal Reverse Transcription [MeSH]
lokal Clinical Laboratory Techniques [MeSH]
lokal Nucleic Acid Amplification Techniques/methods [MeSH]
lokal Genes, Viral [MeSH]
lokal Real-Time Polymerase Chain Reaction [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/TWF1dG5lciwgTGVuYQ==|https://frl.publisso.de/adhoc/uri/QmFpbGxpZSwgQ2hyaXN0aW4tS2lyc3R5|https://frl.publisso.de/adhoc/uri/SGVyb2xkLCBIZWlrZSBNYXJpZQ==|https://frl.publisso.de/adhoc/uri/Vm9sa3dlaW4sIFdvbGZyYW0=|https://frl.publisso.de/adhoc/uri/R3VlcnRsZXIsIFBhdHJpY2s=|https://frl.publisso.de/adhoc/uri/RWJlcmxlLCBVdGU=|https://frl.publisso.de/adhoc/uri/QWNrZXJtYW5uLCBOaWtvbGF1cw==|https://frl.publisso.de/adhoc/uri/U2luZywgQW5kcmVhcw==|https://frl.publisso.de/adhoc/uri/UGF2bG92aWMsIE1lbGFuaWU=|https://frl.publisso.de/adhoc/uri/R29lcmxpY2gsIE90dG1hcg==|https://frl.publisso.de/adhoc/uri/QnVzY2gsIFVscmljaA==|https://frl.publisso.de/adhoc/uri/V2Fzc2lsbCwgTGFycw==|https://frl.publisso.de/adhoc/uri/SHViZXIsIEluZ3JpZA==|https://orcid.org/0000-0002-2625-3802
1000 Hinweis
  • DeepGreen-ID: ceed756b2e2c4641839b4683167b5459 ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
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1000 Erstellt am 2023-05-12T15:30:34.007+0200
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1000 Zuletzt bearbeitet 2023-10-24T08:11:57.275+0200
1000 Objekt bearb. Tue Oct 24 08:11:57 CEST 2023
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