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Strand Displacement Probes Combined with Isothermal Nucleic Acid Amplification for Instrument-Free Detection from Complex Samples
[Image: see text] Sensitive and specific detection of pathogens via nucleic acid amplification is currently constrained to laboratory settings and portable equipment with costly fluorescent detectors. Nucleic acid-detecting lateral flow immunoassay strips (LFIAs) offer a low-cost visual transduction...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990927/ https://www.ncbi.nlm.nih.gov/pubmed/29667809 http://dx.doi.org/10.1021/acs.analchem.8b00269 |
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author | Phillips, Elizabeth A. Moehling, Taylor J. Bhadra, Sanchita Ellington, Andrew D. Linnes, Jacqueline C. |
author_facet | Phillips, Elizabeth A. Moehling, Taylor J. Bhadra, Sanchita Ellington, Andrew D. Linnes, Jacqueline C. |
author_sort | Phillips, Elizabeth A. |
collection | PubMed |
description | [Image: see text] Sensitive and specific detection of pathogens via nucleic acid amplification is currently constrained to laboratory settings and portable equipment with costly fluorescent detectors. Nucleic acid-detecting lateral flow immunoassay strips (LFIAs) offer a low-cost visual transduction strategy at points of need. Unfortunately, these LFIAs frequently detect amplification byproducts that can yield spurious results which can only be deciphered through statistical analysis. We integrated customizable strand displacement probes into standard loop mediated isothermal amplification (LAMP) assays to prevent byproduct capture on commercial LFIAs. We find that combining strand displacement with LAMP (SD-LAMP) yields LFIA test band intensities that can be unequivocally interpreted by human subjects without additional instrumentation, thereby alleviating the need for a portable reader’s analysis. Using SD-LAMP, we capture target amplicons on commercially available LFIAs from as few as 3.5 Vibrio cholerae and 2 750 Escherichia coli bacteria without false positive or false negative interpretation. Moreover, we demonstrate that LFIA capture of SD-LAMP products remain specific even in the presence of complex sample matrixes, providing a significant step toward reliable instrument-free pathogen detection outside of laboratories. |
format | Online Article Text |
id | pubmed-5990927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-59909272018-06-08 Strand Displacement Probes Combined with Isothermal Nucleic Acid Amplification for Instrument-Free Detection from Complex Samples Phillips, Elizabeth A. Moehling, Taylor J. Bhadra, Sanchita Ellington, Andrew D. Linnes, Jacqueline C. Anal Chem [Image: see text] Sensitive and specific detection of pathogens via nucleic acid amplification is currently constrained to laboratory settings and portable equipment with costly fluorescent detectors. Nucleic acid-detecting lateral flow immunoassay strips (LFIAs) offer a low-cost visual transduction strategy at points of need. Unfortunately, these LFIAs frequently detect amplification byproducts that can yield spurious results which can only be deciphered through statistical analysis. We integrated customizable strand displacement probes into standard loop mediated isothermal amplification (LAMP) assays to prevent byproduct capture on commercial LFIAs. We find that combining strand displacement with LAMP (SD-LAMP) yields LFIA test band intensities that can be unequivocally interpreted by human subjects without additional instrumentation, thereby alleviating the need for a portable reader’s analysis. Using SD-LAMP, we capture target amplicons on commercially available LFIAs from as few as 3.5 Vibrio cholerae and 2 750 Escherichia coli bacteria without false positive or false negative interpretation. Moreover, we demonstrate that LFIA capture of SD-LAMP products remain specific even in the presence of complex sample matrixes, providing a significant step toward reliable instrument-free pathogen detection outside of laboratories. American Chemical Society 2018-04-18 2018-06-05 /pmc/articles/PMC5990927/ /pubmed/29667809 http://dx.doi.org/10.1021/acs.analchem.8b00269 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Phillips, Elizabeth A. Moehling, Taylor J. Bhadra, Sanchita Ellington, Andrew D. Linnes, Jacqueline C. Strand Displacement Probes Combined with Isothermal Nucleic Acid Amplification for Instrument-Free Detection from Complex Samples |
title | Strand Displacement Probes Combined with Isothermal
Nucleic Acid Amplification for Instrument-Free Detection from Complex
Samples |
title_full | Strand Displacement Probes Combined with Isothermal
Nucleic Acid Amplification for Instrument-Free Detection from Complex
Samples |
title_fullStr | Strand Displacement Probes Combined with Isothermal
Nucleic Acid Amplification for Instrument-Free Detection from Complex
Samples |
title_full_unstemmed | Strand Displacement Probes Combined with Isothermal
Nucleic Acid Amplification for Instrument-Free Detection from Complex
Samples |
title_short | Strand Displacement Probes Combined with Isothermal
Nucleic Acid Amplification for Instrument-Free Detection from Complex
Samples |
title_sort | strand displacement probes combined with isothermal
nucleic acid amplification for instrument-free detection from complex
samples |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990927/ https://www.ncbi.nlm.nih.gov/pubmed/29667809 http://dx.doi.org/10.1021/acs.analchem.8b00269 |
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