Cargando…

Isothermal amplification of environmental DNA (eDNA) for direct field-based monitoring and laboratory confirmation of Dreissena sp.

Loop-mediated isothermal amplification (LAMP) of aquatic invasive species environmental DNA (AIS eDNA) was used for rapid, sensitive, and specific detection of Dreissena sp. relevant to the Great Lakes (USA) basin. The method was validated for two uses including i) direct amplification of eDNA using...

Descripción completa

Detalles Bibliográficos
Autores principales: Williams, Maggie R., Stedtfeld, Robert D., Engle, Cathrine, Salach, Paul, Fakher, Umama, Stedtfeld, Tiffany, Dreelin, Erin, Stevenson, R. Jan, Latimore, Jo, Hashsham, Syed A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643059/
https://www.ncbi.nlm.nih.gov/pubmed/29036210
http://dx.doi.org/10.1371/journal.pone.0186462
_version_ 1783271459691429888
author Williams, Maggie R.
Stedtfeld, Robert D.
Engle, Cathrine
Salach, Paul
Fakher, Umama
Stedtfeld, Tiffany
Dreelin, Erin
Stevenson, R. Jan
Latimore, Jo
Hashsham, Syed A.
author_facet Williams, Maggie R.
Stedtfeld, Robert D.
Engle, Cathrine
Salach, Paul
Fakher, Umama
Stedtfeld, Tiffany
Dreelin, Erin
Stevenson, R. Jan
Latimore, Jo
Hashsham, Syed A.
author_sort Williams, Maggie R.
collection PubMed
description Loop-mediated isothermal amplification (LAMP) of aquatic invasive species environmental DNA (AIS eDNA) was used for rapid, sensitive, and specific detection of Dreissena sp. relevant to the Great Lakes (USA) basin. The method was validated for two uses including i) direct amplification of eDNA using a hand filtration system and ii) confirmation of the results after DNA extraction using a conventional thermal cycler run at isothermal temperatures. Direct amplification eliminated the need for DNA extraction and purification and allowed detection of target invasive species in grab or concentrated surface water samples, containing both free DNA as well as larger cells and particulates, such as veligers, eggs, or seeds. The direct amplification method validation was conducted using Dreissena polymorpha and Dreissena bugensis and uses up to 1 L grab water samples for high target abundance (e.g., greater than 10 veligers (larval mussels) per L for Dreissena sp.) or 20 L samples concentrated through 35 μm nylon screens for low target abundance, at less than 10 veligers per liter water. Surface water concentrate samples were collected over a period of three years, mostly from inland lakes in Michigan with the help of a network of volunteers. Field samples collected from 318 surface water locations included i) filtered concentrate for direct amplification validation and ii) 1 L grab water sample for eDNA extraction and confirmation. Though the extraction-based protocol was more sensitive (resulting in more positive detections than direct amplification), direct amplification could be used for rapid screening, allowing for quicker action times. For samples collected between May and August, results of eDNA direct amplification were consistent with known presence/absence of selected invasive species. A cross-platform smartphone application was also developed to disseminate the analyzed results to volunteers. Field tests of the direct amplification protocol using a portable device (Gene-Z) showed the method could be used in the field to obtain results within one hr (from sample to result). Overall, the direct amplification has the potential to simplify the eDNA-based monitoring of multiple aquatic invasive species. Additional studies are warranted to establish quantitative correlation between eDNA copy number, veliger, biomass or organismal abundance in the field.
format Online
Article
Text
id pubmed-5643059
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-56430592017-10-30 Isothermal amplification of environmental DNA (eDNA) for direct field-based monitoring and laboratory confirmation of Dreissena sp. Williams, Maggie R. Stedtfeld, Robert D. Engle, Cathrine Salach, Paul Fakher, Umama Stedtfeld, Tiffany Dreelin, Erin Stevenson, R. Jan Latimore, Jo Hashsham, Syed A. PLoS One Research Article Loop-mediated isothermal amplification (LAMP) of aquatic invasive species environmental DNA (AIS eDNA) was used for rapid, sensitive, and specific detection of Dreissena sp. relevant to the Great Lakes (USA) basin. The method was validated for two uses including i) direct amplification of eDNA using a hand filtration system and ii) confirmation of the results after DNA extraction using a conventional thermal cycler run at isothermal temperatures. Direct amplification eliminated the need for DNA extraction and purification and allowed detection of target invasive species in grab or concentrated surface water samples, containing both free DNA as well as larger cells and particulates, such as veligers, eggs, or seeds. The direct amplification method validation was conducted using Dreissena polymorpha and Dreissena bugensis and uses up to 1 L grab water samples for high target abundance (e.g., greater than 10 veligers (larval mussels) per L for Dreissena sp.) or 20 L samples concentrated through 35 μm nylon screens for low target abundance, at less than 10 veligers per liter water. Surface water concentrate samples were collected over a period of three years, mostly from inland lakes in Michigan with the help of a network of volunteers. Field samples collected from 318 surface water locations included i) filtered concentrate for direct amplification validation and ii) 1 L grab water sample for eDNA extraction and confirmation. Though the extraction-based protocol was more sensitive (resulting in more positive detections than direct amplification), direct amplification could be used for rapid screening, allowing for quicker action times. For samples collected between May and August, results of eDNA direct amplification were consistent with known presence/absence of selected invasive species. A cross-platform smartphone application was also developed to disseminate the analyzed results to volunteers. Field tests of the direct amplification protocol using a portable device (Gene-Z) showed the method could be used in the field to obtain results within one hr (from sample to result). Overall, the direct amplification has the potential to simplify the eDNA-based monitoring of multiple aquatic invasive species. Additional studies are warranted to establish quantitative correlation between eDNA copy number, veliger, biomass or organismal abundance in the field. Public Library of Science 2017-10-16 /pmc/articles/PMC5643059/ /pubmed/29036210 http://dx.doi.org/10.1371/journal.pone.0186462 Text en © 2017 Williams et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Williams, Maggie R.
Stedtfeld, Robert D.
Engle, Cathrine
Salach, Paul
Fakher, Umama
Stedtfeld, Tiffany
Dreelin, Erin
Stevenson, R. Jan
Latimore, Jo
Hashsham, Syed A.
Isothermal amplification of environmental DNA (eDNA) for direct field-based monitoring and laboratory confirmation of Dreissena sp.
title Isothermal amplification of environmental DNA (eDNA) for direct field-based monitoring and laboratory confirmation of Dreissena sp.
title_full Isothermal amplification of environmental DNA (eDNA) for direct field-based monitoring and laboratory confirmation of Dreissena sp.
title_fullStr Isothermal amplification of environmental DNA (eDNA) for direct field-based monitoring and laboratory confirmation of Dreissena sp.
title_full_unstemmed Isothermal amplification of environmental DNA (eDNA) for direct field-based monitoring and laboratory confirmation of Dreissena sp.
title_short Isothermal amplification of environmental DNA (eDNA) for direct field-based monitoring and laboratory confirmation of Dreissena sp.
title_sort isothermal amplification of environmental dna (edna) for direct field-based monitoring and laboratory confirmation of dreissena sp.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643059/
https://www.ncbi.nlm.nih.gov/pubmed/29036210
http://dx.doi.org/10.1371/journal.pone.0186462
work_keys_str_mv AT williamsmaggier isothermalamplificationofenvironmentaldnaednafordirectfieldbasedmonitoringandlaboratoryconfirmationofdreissenasp
AT stedtfeldrobertd isothermalamplificationofenvironmentaldnaednafordirectfieldbasedmonitoringandlaboratoryconfirmationofdreissenasp
AT englecathrine isothermalamplificationofenvironmentaldnaednafordirectfieldbasedmonitoringandlaboratoryconfirmationofdreissenasp
AT salachpaul isothermalamplificationofenvironmentaldnaednafordirectfieldbasedmonitoringandlaboratoryconfirmationofdreissenasp
AT fakherumama isothermalamplificationofenvironmentaldnaednafordirectfieldbasedmonitoringandlaboratoryconfirmationofdreissenasp
AT stedtfeldtiffany isothermalamplificationofenvironmentaldnaednafordirectfieldbasedmonitoringandlaboratoryconfirmationofdreissenasp
AT dreelinerin isothermalamplificationofenvironmentaldnaednafordirectfieldbasedmonitoringandlaboratoryconfirmationofdreissenasp
AT stevensonrjan isothermalamplificationofenvironmentaldnaednafordirectfieldbasedmonitoringandlaboratoryconfirmationofdreissenasp
AT latimorejo isothermalamplificationofenvironmentaldnaednafordirectfieldbasedmonitoringandlaboratoryconfirmationofdreissenasp
AT hashshamsyeda isothermalamplificationofenvironmentaldnaednafordirectfieldbasedmonitoringandlaboratoryconfirmationofdreissenasp