Evidence map›Paper›PMID 38820540›Full record

ArticlePLoS genetics2024

Adaptations to nitrogen availability drive ecological divergence of chemosynthetic symbionts.

Isidora Morel-Letelier, Benedict Yuen, A Carlotta Kück, Yolanda E Camacho-García, Jillian M Petersen, Minor Lara, Matthieu Leray, Jonathan A Eisen, Jay T Osvatic, Olivier Gros and 1 more

Abstract read
In one paragraph

Article in PLoS genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
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

11 authors.

Isidora Morel-LetelierEco-Evolutionary Interactions Group, Max Planck Institute for Marine Microbiology (MPIMM), Bremen, Germany.ORCID 0000-0003-1402-2393
Benedict YuenEco-Evolutionary Interactions Group, Max Planck Institute for Marine Microbiology (MPIMM), Bremen, Germany.ORCID 0000-0002-4979-0862
A Carlotta KückEco-Evolutionary Interactions Group, Max Planck Institute for Marine Microbiology (MPIMM), Bremen, Germany.
Yolanda E Camacho-GarcíaCentro de Investigación en Ciencias del Mar y Limnología (CIMAR), Universidad de Costa Rica, San Pedro, San José, Costa Rica.
Jillian M PetersenCentre for Microbiology and Environmental Systems Science, University of Vienna, Vienna, Austria.ORCID 0000-0002-9852-3445
Minor LaraDiving Center Cuajiniquil, Provincia de Guanacaste, Cuajiniquil, Costa Rica.
Matthieu LeraySmithsonian Tropical Research Institute, Balboa, Ancon, Republic of Panamá.
Jonathan A EisenDepartment of Evolution and Ecology, University of California, Davis, Davis, California, United States of America.ORCID 0000-0002-0159-2197
Jay T OsvaticJoint Microbiome Facility of the Medical University of Vienna and the University of Vienna, Vienna, Austria.
Olivier GrosInstitut de Systématique, Evolution, Biodiversité (ISYEB), Muséum National d'Histoire Naturelle, CNRS, Sorbonne Université, Université des Antilles, Pointe-à-Pitre, France.
Laetitia G E WilkinsEco-Evolutionary Interactions Group, Max Planck Institute for Marine Microbiology (MPIMM), Bremen, Germany.ORCID 0000-0003-3632-2063

Funding

Acquisition of Covaris E220 and Sciclone G3 systems for high throughput sequencinS10OD010786 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI COMAI, LUCA · 2012 to 2012
$311k
Austrian Science Fund FWF DOC 69NIH HHS S10 OD010786
6 · The paper itself

Abstract

Bacterial symbionts, with their shorter generation times and capacity for horizontal gene transfer (HGT), play a critical role in allowing marine organisms to cope with environmental change. The closure of the Isthmus of Panama created distinct environmental conditions in the Tropical Eastern Pacific (TEP) and Caribbean, offering a "natural experiment" for studying how closely related animals evolve and adapt under environmental change. However, the role of bacterial symbionts in this process is often overlooked. We sequenced the genomes of endosymbiotic bacteria in two sets of sister species of chemosymbiotic bivalves from the genera Codakia and Ctena (family Lucinidae) collected on either side of the Isthmus, to investigate how differing environmental conditions have influenced the selection of symbionts and their metabolic capabilities. The lucinid sister species hosted different Candidatus Thiodiazotropha symbionts and only those from the Caribbean had the genetic potential for nitrogen fixation, while those from the TEP did not. Interestingly, this nitrogen-fixing ability did not correspond to symbiont phylogeny, suggesting convergent evolution of nitrogen fixation potential under nutrient-poor conditions. Reconstructing the evolutionary history of the nifHDKT operon by including other lucinid symbiont genomes from around the world further revealed that the last common ancestor (LCA) of Ca. Thiodiazotropha lacked nif genes, and populations in oligotrophic habitats later re-acquired the nif operon through HGT from the Sedimenticola symbiont lineage. Our study suggests that HGT of the nif operon has facilitated niche diversification of the globally distributed Ca. Thiodiazotropha endolucinida species clade. It highlights the importance of nitrogen availability in driving the ecological diversification of chemosynthetic symbiont species and the role that bacterial symbionts may play in the adaptation of marine organisms to changing environmental conditions.

Indexed as

BivalviaGene Transfer, HorizontalNitrogenNitrogen FixationPhylogenySymbiosisAdaptation, PhysiologicalAnimalsBacteriaCaribbean RegionGenome, BacterialPanamaNitrogen

Identifiers

PMID38820540
PMCPMC11168628

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.