Evidence map›Paper›PMID 34078452›Full record

ArticleMicrobiome2021

Holobiont nitrogen control and its potential for eutrophication resistance in an obligate photosymbiotic jellyfish.

Till Röthig, Giulia Puntin, Jane C Y Wong, Alfred Burian, Wendy McLeod, David M Baker

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Microbiome, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

9 citing papers in PubMed, 28 citations in OpenAlex.

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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

6 authors at 5 institutions in 4 countries.

Till Röthig *The Swire Institute of Marine Science and School of Biological Sciences, The University of Hong Kong, Hong Kong, Hong Kong, SAR of China. tillroethig@gmail.com.ORCID 0000-0001-6359-8589
Giulia Puntin *The Swire Institute of Marine Science and School of Biological Sciences, The University of Hong Kong, Hong Kong, Hong Kong, SAR of China.
Jane C Y WongThe Swire Institute of Marine Science and School of Biological Sciences, The University of Hong Kong, Hong Kong, Hong Kong, SAR of China.
Alfred BurianMarine Ecology Department, Lurio University, Nampula, Mozambique.
Wendy McLeodThe Swire Institute of Marine Science and School of Biological Sciences, The University of Hong Kong, Hong Kong, Hong Kong, SAR of China.
David M BakerThe Swire Institute of Marine Science and School of Biological Sciences, The University of Hong Kong, Hong Kong, Hong Kong, SAR of China. dmbaker@hku.hk.
University of Hong Kong · HKHelmholtz Centre for Environmental Research · DEIstituto di Scienze Marine del Consiglio Nazionale delle Ricerche · ITJustus-Liebig-Universität Gießen · DEUniversity of Konstanz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMarine holobionts depend on microbial members for health and nutrient cycling. This is particularly evident in cnidarian-algae symbioses that facilitate energy and nutrient acquisition. However, this partnership is highly sensitive to environmental change-including eutrophication-that causes dysbiosis and contributes to global coral reef decline. Yet, some holobionts exhibit resistance to dysbiosis in eutrophic environments, including the obligate photosymbiotic scyphomedusa Cassiopea xamachana.

methodsOur aim was to assess the mechanisms in C. xamachana that stabilize symbiotic relationships. We combined labelled bicarbonate (

resultsC-fixation and cycling by algal Symbiodiniaceae was essential for C. xamachana as even at high heterotrophic feeding rates aposymbiotic medusae continuously lost weight. Heterotrophically acquired C and N were readily shared among host and algae. This was in sharp contrast to nitrate assimilation by Symbiodiniaceae, which appeared to be strongly restricted. Instead, the bacterial microbiome seemed to play a major role in the holobiont's DIN assimilation as uptake rates showed a significant positive relationship with phylogenetic diversity of medusa-associated bacteria. This is corroborated by inferred functional capacity that links the dominant bacterial taxa (~90 %) to nitrogen cycling. Observed bacterial community structure differed between apo- and symbiotic C. xamachana putatively highlighting enrichment of ammonium oxidizers and nitrite reducers and depletion of nitrogen-fixers in symbiotic medusae.

conclusionHost, algal symbionts, and bacterial associates contribute to regulated nutrient assimilation and cycling in C. xamachana. We found that the bacterial microbiome of symbiotic medusae was seemingly structured to increase DIN removal and enforce algal N-limitation-a mechanism that would help to stabilize the host-algae relationship even under eutrophic conditions. Video abstract.

Indexed as

AnthozoaCnidariaDinoflagellidaAnimalsEutrophicationNitrogenPhylogenySymbiosisNitrogen16S rRNA geneBacterial profilingEnvironmental resilienceStable isotope analysisTracer

Identifiers

PMID34078452
PMCPMC8173792
OpenAlexW3130991180

What OpenQuestion holds

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Registered trials

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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.