Dead‐end hollow fiber ultrafiltration capture of environmental DNA for freshwater mussel (Unionidae) species detection with metabarcoding

Author:

McKee Anna M.1ORCID,Klymus Katy E.2ORCID,Lor Yer3ORCID,Kaminski Marissa3ORCID,Tajjioui Tariq3ORCID,Johnson Nathan A.4ORCID,Carroll Matt5ORCID,Goodson Chris5ORCID,Spear Stephen F.3ORCID

Affiliation:

1. U.S. Geological Survey South Atlantic Water Science Center Norcross Georgia USA

2. U.S. Geological Survey Columbia Environmental Research Center Columbia Missouri USA

3. U.S. Geological Survey Upper Midwest Environmental Sciences Center La Crosse Wisconsin USA

4. U.S. Geological Survey Wetland and Aquatic Research Center Gainesville Florida USA

5. Georgia Department of Transportation Atlanta Georgia USA

Abstract

AbstractInsufficient water sample volumes can be a limiting factor for detecting species with environmental DNA (eDNA) from aquatic habitats. We compared detections of freshwater mussel (Unionidae) communities using large water sample volumes and dead‐end hollow fiber ultrafiltration (D‐HFUF or DEUF) with traditional eDNA filtration methods that use relatively small water sample volumes. Unionid species were detected in approximately 50‐L D‐HFUF eDNA samples with two mitochondrial DNA metabarcoding markers (COI and ND1) and compared to species detection results from eDNA captured from commonly used 1‐L samples filtered with polyethersulfone (PES) filters at three lotic sites in Georgia and Missouri. Of the 431,560 COI and 1,035,472 ND1 reads from all environmental samples of both filter types that passed quality control, 95% (410,755 reads) of COI reads and 85% (883,472 reads) of ND1 reads were assigned to a unionid species. Nineteen different freshwater mussel species were detected across all D‐HFUF samples, and 11 species were detected across all PES samples. Reads assigned to the genus Elliptio could not be resolved beyond the genus level with either marker. From D‐HFUF samples, 15 and 16 mussel species were detected with the COI and ND1 markers, respectively. From PES samples, nine and seven species were detected with the COI and ND1 markers, respectively. More mussel species were detected at each site in D‐HFUF samples than in PES samples regardless of whether results from both markers were combined or evaluated separately. Our results demonstrate the merit of further exploration and optimization of D‐HFUF for capturing eDNA from high‐volume water samples to facilitate detection of unionids and likely other aquatic organisms.

Publisher

Wiley

Subject

Genetics,Ecology,Ecology, Evolution, Behavior and Systematics

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