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DNA-based species detection capabilities using laser transmission spectroscopy

Early detection of invasive species is critical for effective biocontrol to mitigate potential ecological and economic damage. Laser transmission spectroscopy (LTS) is a powerful solution offering real-time, DNA-based species detection in the field. LTS can measure the size, shape and number of nano...

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Detalles Bibliográficos
Autores principales: Mahon, A. R., Barnes, M. A., Li, F., Egan, S. P., Tanner, C. E., Ruggiero, S. T., Feder, J. L., Lodge, D. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3565792/
https://www.ncbi.nlm.nih.gov/pubmed/23015524
http://dx.doi.org/10.1098/rsif.2012.0637
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author Mahon, A. R.
Barnes, M. A.
Li, F.
Egan, S. P.
Tanner, C. E.
Ruggiero, S. T.
Feder, J. L.
Lodge, D. M.
author_facet Mahon, A. R.
Barnes, M. A.
Li, F.
Egan, S. P.
Tanner, C. E.
Ruggiero, S. T.
Feder, J. L.
Lodge, D. M.
author_sort Mahon, A. R.
collection PubMed
description Early detection of invasive species is critical for effective biocontrol to mitigate potential ecological and economic damage. Laser transmission spectroscopy (LTS) is a powerful solution offering real-time, DNA-based species detection in the field. LTS can measure the size, shape and number of nanoparticles in a solution and was used here to detect size shifts resulting from hybridization of the polymerase chain reaction product to nanoparticles functionalized with species-specific oligonucleotide probes or with the species-specific oligonucleotide probes alone. We carried out a series of DNA detection experiments using the invasive freshwater quagga mussel (Dreissena bugensis) to evaluate the capability of the LTS platform for invasive species detection. Specifically, we tested LTS sensitivity to (i) DNA concentrations of a single target species, (ii) the presence of a target species within a mixed sample of other closely related species, (iii) species-specific functionalized nanoparticles versus species-specific oligonucleotide probes alone, and (iv) amplified DNA fragments versus unamplified genomic DNA. We demonstrate that LTS is a highly sensitive technique for rapid target species detection, with detection limits in the picomolar range, capable of successful identification in multispecies samples containing target and non-target species DNA. These results indicate that the LTS DNA detection platform will be useful for field application of target species. Additionally, we find that LTS detection is effective with species-specific oligonucleotide tags alone or when they are attached to polystyrene nanobeads and with both amplified and unamplified DNA, indicating that the technique may also have versatility for broader applications.
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spelling pubmed-35657922013-02-13 DNA-based species detection capabilities using laser transmission spectroscopy Mahon, A. R. Barnes, M. A. Li, F. Egan, S. P. Tanner, C. E. Ruggiero, S. T. Feder, J. L. Lodge, D. M. J R Soc Interface Research Articles Early detection of invasive species is critical for effective biocontrol to mitigate potential ecological and economic damage. Laser transmission spectroscopy (LTS) is a powerful solution offering real-time, DNA-based species detection in the field. LTS can measure the size, shape and number of nanoparticles in a solution and was used here to detect size shifts resulting from hybridization of the polymerase chain reaction product to nanoparticles functionalized with species-specific oligonucleotide probes or with the species-specific oligonucleotide probes alone. We carried out a series of DNA detection experiments using the invasive freshwater quagga mussel (Dreissena bugensis) to evaluate the capability of the LTS platform for invasive species detection. Specifically, we tested LTS sensitivity to (i) DNA concentrations of a single target species, (ii) the presence of a target species within a mixed sample of other closely related species, (iii) species-specific functionalized nanoparticles versus species-specific oligonucleotide probes alone, and (iv) amplified DNA fragments versus unamplified genomic DNA. We demonstrate that LTS is a highly sensitive technique for rapid target species detection, with detection limits in the picomolar range, capable of successful identification in multispecies samples containing target and non-target species DNA. These results indicate that the LTS DNA detection platform will be useful for field application of target species. Additionally, we find that LTS detection is effective with species-specific oligonucleotide tags alone or when they are attached to polystyrene nanobeads and with both amplified and unamplified DNA, indicating that the technique may also have versatility for broader applications. The Royal Society 2013-01-06 /pmc/articles/PMC3565792/ /pubmed/23015524 http://dx.doi.org/10.1098/rsif.2012.0637 Text en http://creativecommons.org/licenses/by/3.0/ © 2012 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research Articles
Mahon, A. R.
Barnes, M. A.
Li, F.
Egan, S. P.
Tanner, C. E.
Ruggiero, S. T.
Feder, J. L.
Lodge, D. M.
DNA-based species detection capabilities using laser transmission spectroscopy
title DNA-based species detection capabilities using laser transmission spectroscopy
title_full DNA-based species detection capabilities using laser transmission spectroscopy
title_fullStr DNA-based species detection capabilities using laser transmission spectroscopy
title_full_unstemmed DNA-based species detection capabilities using laser transmission spectroscopy
title_short DNA-based species detection capabilities using laser transmission spectroscopy
title_sort dna-based species detection capabilities using laser transmission spectroscopy
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3565792/
https://www.ncbi.nlm.nih.gov/pubmed/23015524
http://dx.doi.org/10.1098/rsif.2012.0637
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