Evaluating sediment and water sampling methods for the estimation of deep-sea biodiversity using environmental DNA.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
12 04 2021
Historique:
received: 18 11 2020
accepted: 15 03 2021
entrez: 13 4 2021
pubmed: 14 4 2021
medline: 9 11 2021
Statut: epublish

Résumé

Despite representing one of the largest biomes on earth, biodiversity of the deep seafloor is still poorly known. Environmental DNA metabarcoding offers prospects for fast inventories and surveys, yet requires standardized sampling approaches and careful choice of environmental substrate. Here, we aimed to optimize the genetic assessment of prokaryote (16S), protistan (18S V4), and metazoan (18S V1-V2, COI) communities, by evaluating sampling strategies for sediment and aboveground water, deployed simultaneously at one deep-sea site. For sediment, while size-class sorting through sieving had no significant effect on total detected alpha diversity and resolved similar taxonomic compositions at the phylum level for all markers studied, it effectively increased the detection of meiofauna phyla. For water, large volumes obtained from an in situ pump (~ 6000 L) detected significantly more metazoan diversity than 7.5 L collected in sampling boxes. However, the pump being limited by larger mesh sizes (> 20 µm), only captured a fraction of microbial diversity, while sampling boxes allowed access to the pico- and nanoplankton. More importantly, communities characterized by aboveground water samples significantly differed from those characterized by sediment, whatever volume used, and both sample types only shared between 3 and 8% of molecular units. Together, these results underline that sediment sieving may be recommended when targeting metazoans, and aboveground water does not represent an alternative to sediment sampling for inventories of benthic diversity.

Identifiants

pubmed: 33846371
doi: 10.1038/s41598-021-86396-8
pii: 10.1038/s41598-021-86396-8
pmc: PMC8041860
doi:

Substances chimiques

Biomarkers 0
DNA, Environmental 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

7856

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Auteurs

Miriam I Brandt (MI)

MARBEC, IFREMER, IRD, CNRS, Univ Montpellier, Sète, France. miriam.isabelle.brandt@gmail.com.

Florence Pradillon (F)

Centre Brest, Laboratoire Environnement Profond (REM/EEP/LEP), IFREMER, CS10070, 29280, Plouzané, France.

Blandine Trouche (B)

IFREMER, CNRS, Laboratoire de Microbiologie Des Environnements Extrêmes (LM2E), Univ Brest, Plouzané, France.

Nicolas Henry (N)

CNRS, Station Biologique de Roscoff, AD2M, UMR 7144, Sorbonne University, 29680, Roscoff, France.

Cathy Liautard-Haag (C)

MARBEC, IFREMER, IRD, CNRS, Univ Montpellier, Sète, France.

Marie-Anne Cambon-Bonavita (MA)

IFREMER, CNRS, Laboratoire de Microbiologie Des Environnements Extrêmes (LM2E), Univ Brest, Plouzané, France.

Valérie Cueff-Gauchard (V)

IFREMER, CNRS, Laboratoire de Microbiologie Des Environnements Extrêmes (LM2E), Univ Brest, Plouzané, France.

Patrick Wincker (P)

Génomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS, Univ of Évry, Paris-Saclay University, 91057, Evry, France.

Caroline Belser (C)

Génomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS, Univ of Évry, Paris-Saclay University, 91057, Evry, France.

Julie Poulain (J)

Génomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS, Univ of Évry, Paris-Saclay University, 91057, Evry, France.

Sophie Arnaud-Haond (S)

MARBEC, IFREMER, IRD, CNRS, Univ Montpellier, Sète, France. sophie.arnaud@ifremer.fr.

Daniela Zeppilli (D)

Centre Brest, Laboratoire Environnement Profond (REM/EEP/LEP), IFREMER, CS10070, 29280, Plouzané, France.

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