Norwegian deep-water coral reefs: cultivation and molecular analysis of planktonic microbial communities

Summary Deep‐sea coral reefs do not receive sunlight and depend on plankton. Little is known about the plankton composition at such reefs, even though they constitute habitats for many invertebrates and fish. We investigated plankton communities from three reefs at 260–350 m depth at hydrocarbon fie...

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Veröffentlicht in:Environmental microbiology 2015-10, Vol.17 (10), p.3597-3609
Hauptverfasser: Jensen, Sigmund, Lynch, Michael D. J., Ray, Jessica L., Neufeld, Josh D., Hovland, Martin
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container_end_page 3609
container_issue 10
container_start_page 3597
container_title Environmental microbiology
container_volume 17
creator Jensen, Sigmund
Lynch, Michael D. J.
Ray, Jessica L.
Neufeld, Josh D.
Hovland, Martin
description Summary Deep‐sea coral reefs do not receive sunlight and depend on plankton. Little is known about the plankton composition at such reefs, even though they constitute habitats for many invertebrates and fish. We investigated plankton communities from three reefs at 260–350 m depth at hydrocarbon fields off the mid‐Norwegian coast using a combination of cultivation and small subunit (SSU) rRNA gene and transcript sequencing. Eight months incubations of a reef water sample with minimal medium, supplemented with carbon dioxide and gaseous alkanes at in situ‐like conditions, enabled isolation of mostly Alphaproteobacteria (Sulfitobacter, Loktanella), Gammaproteobacteria (Colwellia) and Flavobacteria (Polaribacter). The relative abundance of isolates in the original sample ranged from ∼ 0.01% to 0.80%. Comparisons of bacterial SSU sequences from filtered plankton of reef and non‐reef control samples indicated high abundance and metabolic activity of primarily Alphaproteobacteria (SAR11 Ia), Gammaproteobacteria (ARCTIC96BD‐19), but also of Deltaproteobacteria (Nitrospina, SAR324). Eukaryote SSU sequences indicated metabolically active microalgae and animals, including codfish, at the reef sites. The plankton community composition varied between reefs and differed between DNA and RNA assessments. Over 5000 operational taxonomic units were detected, some indicators of reef sites (e.g. Flavobacteria, Cercozoa, Demospongiae) and some more active at reef sites (e.g. Gammaproteobacteria, Ciliophora, Copepoda).
doi_str_mv 10.1111/1462-2920.12531
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Eight months incubations of a reef water sample with minimal medium, supplemented with carbon dioxide and gaseous alkanes at in situ‐like conditions, enabled isolation of mostly Alphaproteobacteria (Sulfitobacter, Loktanella), Gammaproteobacteria (Colwellia) and Flavobacteria (Polaribacter). The relative abundance of isolates in the original sample ranged from ∼ 0.01% to 0.80%. Comparisons of bacterial SSU sequences from filtered plankton of reef and non‐reef control samples indicated high abundance and metabolic activity of primarily Alphaproteobacteria (SAR11 Ia), Gammaproteobacteria (ARCTIC96BD‐19), but also of Deltaproteobacteria (Nitrospina, SAR324). Eukaryote SSU sequences indicated metabolically active microalgae and animals, including codfish, at the reef sites. The plankton community composition varied between reefs and differed between DNA and RNA assessments. 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Eight months incubations of a reef water sample with minimal medium, supplemented with carbon dioxide and gaseous alkanes at in situ‐like conditions, enabled isolation of mostly Alphaproteobacteria (Sulfitobacter, Loktanella), Gammaproteobacteria (Colwellia) and Flavobacteria (Polaribacter). The relative abundance of isolates in the original sample ranged from ∼ 0.01% to 0.80%. Comparisons of bacterial SSU sequences from filtered plankton of reef and non‐reef control samples indicated high abundance and metabolic activity of primarily Alphaproteobacteria (SAR11 Ia), Gammaproteobacteria (ARCTIC96BD‐19), but also of Deltaproteobacteria (Nitrospina, SAR324). Eukaryote SSU sequences indicated metabolically active microalgae and animals, including codfish, at the reef sites. The plankton community composition varied between reefs and differed between DNA and RNA assessments. Over 5000 operational taxonomic units were detected, some indicators of reef sites (e.g. Flavobacteria, Cercozoa, Demospongiae) and some more active at reef sites (e.g. Gammaproteobacteria, Ciliophora, Copepoda).</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>24911121</pmid><doi>10.1111/1462-2920.12531</doi><tpages>13</tpages></addata></record>
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subjects Alphaproteobacteria - genetics
Alphaproteobacteria - growth & development
Alphaproteobacteria - isolation & purification
Animals
Anthozoa - microbiology
Base Sequence
Ciliophora
Colwellia
Copepoda
Coral Reefs
Deltaproteobacteria - genetics
Deltaproteobacteria - growth & development
Deltaproteobacteria - isolation & purification
Demospongiae
Ecosystem
Flavobacteria
Flavobacteriaceae - genetics
Flavobacteriaceae - growth & development
Flavobacteriaceae - isolation & purification
Gadus
Gammaproteobacteria - genetics
Gammaproteobacteria - growth & development
Gammaproteobacteria - isolation & purification
Microbial Consortia - physiology
Molecular Sequence Data
Norway
Plankton
Plankton - genetics
Plankton - growth & development
Polaribacter
Seawater - microbiology
Sulfitobacter
title Norwegian deep-water coral reefs: cultivation and molecular analysis of planktonic microbial communities
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