z-logo
open-access-imgOpen Access
Quantifying Environmental DNA Signals for Aquatic Invasive Species Across Multiple Detection Platforms
Author(s) -
Lucas M. Nathan,
Megan Simmons,
Benjamin J. Wegleitner,
Christopher L. Jerde,
Andrew R. Mahon
Publication year - 2014
Publication title -
environmental science and technology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.851
H-Index - 397
eISSN - 1520-5851
pISSN - 0013-936X
DOI - 10.1021/es5034052
Subject(s) - digital polymerase chain reaction , environmental dna , mesocosm , biology , polymerase chain reaction , real time polymerase chain reaction , population , sampling (signal processing) , computational biology , sample (material) , ecology , ecosystem , genetics , computer science , biodiversity , chemistry , chromatography , gene , demography , filter (signal processing) , sociology , computer vision
The use of molecular surveillance techniques has become popular among aquatic researchers and managers due to the improved sensitivity and efficiency compared to traditional sampling methods. Rapid expansion in the use of environmental DNA (eDNA), paired with the advancement of molecular technologies, has resulted in new detection platforms and techniques. In this study we present a comparison of three eDNA surveillance platforms: traditional polymerase chain reaction (PCR), quantitative PCR (qPCR), and digital droplet PCR (ddPCR) in which water samples were collected over a 24 h time period from mesocosm experiments containing a population gradient of invasive species densities. All platforms reliably detected the presence of DNA, even at low target organism densities within the first hour. The two quantitative platforms (qPCR and ddPCR) produced similar estimates of DNA concentrations. The analyses completed with ddPCR was faster from sample collection through analyses and cost approximately half the expenditure of qPCR. Although a new platform for eDNA surveillance of aquatic species, ddPCR was consistent with more commonly used qPCR and a cost-effective means of estimating DNA concentrations. Use of ddPCR by researchers and managers should be considered in future eDNA surveillance applications.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom