Evidence map›Paper›PMID 29374496›Full record

ArticleMicrobiome2018

Metagenomic investigation of vestimentiferan tubeworm endosymbionts from Mid-Cayman Rise reveals new insights into metabolism and diversity.

Julie Reveillaud, Rika Anderson, Sintra Reves-Sohn, Colleen Cavanaugh, Julie A Huber

Open access · goldAbstract read
In one paragraph

Article in Microbiome, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
7.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 52 citations in OpenAlex.

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  8. Symbiont Community Composition inApplied and environmental microbiology · 2022
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  16. Siboglinids (Annelida, Siboglinidae) as Possible Hydrocarbon Indicators as Exemplified by the Sea of Okhotsk.Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections · 2019
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 2 countries.

Julie ReveillaudASTRE, INRA, CIRAD, University of Montpellier, Montpellier, France. julie.reveillaud@supagro.inra.fr.
Rika AndersonJosephine Bay Paul Center, Marine Biological Laboratory, Woods Hole, MA, USA.
Sintra Reves-SohnJosephine Bay Paul Center, Marine Biological Laboratory, Woods Hole, MA, USA.
Colleen CavanaughDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, USA.
Julie A HuberJosephine Bay Paul Center, Marine Biological Laboratory, Woods Hole, MA, USA.
Marine Biological Laboratory · USAnimal, Santé, Territoires, Risques et Ecosystèmes · FRHarvard University · USLaboratoire de Biotechnologie et Chimie Marines · FR

Funding

NASA grant NNX-32709AB75GNational Science Foundation C-DEBI
6 · The paper itself

Abstract

backgroundThe microbial endosymbionts of two species of vestimentiferan tubeworms (Escarpia sp. and Lamellibrachia sp.2) collected from an area of low-temperature hydrothermal diffuse vent flow at the Mid-Cayman Rise (MCR) in the Caribbean Sea were characterized using microscopy, phylogenetic analyses, and a metagenomic approach.

resultsBacteria, with a typical Gram negative cell envelope contained within membrane-bound vacuoles, were observed within the trophosome of both tubeworm species. Phylogenetic analysis of the 16S rRNA gene and ITS region suggested MCR individuals harbored highly similar endosymbionts that were > 98% identical, with the exception of two symbionts that showed a 60 bp insertion within the ITS region. All sequences from MCR endosymbionts formed a separate well-supported clade that diverged from those of symbionts of seep and vent vestimentiferans from the Pacific, Gulf of Mexico, and Mediterranean Sea. The metagenomes of the symbionts of two specimens of each tubeworm species were sequenced, and two distinct Gammaproteobacteria metagenome-assembled genomes (MAGs) of more than 4 Mbp assembled. An Average Nucleotide Identity (ANI) of 86.5% between these MAGs, together with distinct 16S rRNA gene and ITS sequences, indicate the presence of multiple endosymbiont phylotypes at the MCR, with one MAG shared between one Escarpia and two Lamellibrachia individuals, indicating these endosymbionts are not specific to either host species. Genes for sulfur and hydrogen oxidation, nitrate reduction (assimilatory and dissimilatory), glycolysis and the Krebs cycle, peptide, sugar, and lipid transporters, and both rTCA and CBB carbon fixation cycles were detected in the MAGs, highlighting key and shared functions with symbiont metagenomes of the vestimentiferans Riftia, Tevnia, and Ridgeia from the Pacific. The potential for a second hydrogen oxidation pathway (via a bidirectional hydrogenase), formate dehydrogenase, a catalase, and several additional peptide transporters were found exclusively in the MCR endosymbiont MAGs.

conclusionsThe present study adds new evidence that tubeworm endosymbionts can potentially switch from autotrophic to heterotrophic metabolism, or may be mixotrophic, presumably while free-living, and also suggests their versatile metabolic potential may enable both the host and symbionts to exploit a wide range of environmental conditions. Together, the marked gene content and sequence dissimilarity at the rRNA operon and whole genome level between vent and seep symbionts suggest these newly described endosymbionts from the MCR belong to a novel tubeworm endosymbiont genera, introduced as Candidatus Vondammii.

Indexed as

AnimalsAutotrophic ProcessesBacteriaGenes, BacterialHydrothermal VentsMetagenomicsPhylogenyPolychaetaRNA, Ribosomal, 16SSymbiosisRNA, Ribosomal, 16S

Identifiers

PMID29374496
PMCPMC5787263
OpenAlexW2785776312

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.