Evidence map›Paper›PMID 27447951›Full record

ArticleNature communications2016

Metabolic modelling reveals the specialization of secondary replicons for niche adaptation in Sinorhizobium meliloti.

George C diCenzo, Alice Checcucci, Marco Bazzicalupo, Alessio Mengoni, Carlo Viti, Lukasz Dziewit, Turlough M Finan, Marco Galardini, Marco Fondi

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
28.1field-weighted citation impact, top 1% 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

48 citing papers in PubMed, 96 citations in OpenAlex.

  1. Review
  2. Article
  3. Mobile gene clusters and coexpressed plant-rhizobium pathways drive partner quality variation in symbiosis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Reconstruction of the genome-scale metabolic network model ofFrontiers in bioengineering and biotechnology · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. How Rhizobia Adapt to the Nodule Environment.Journal of bacteriology · 2021
    Article
  19. Article
  20. 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

9 authors at 4 institutions in 4 countries.

George C diCenzoDepartment of Biology, McMaster University, Hamilton, Ontario, Canada L8S 1A1.
Alice CheccucciDepartment of Biology, University of Florence, 50019 Sesto Fiorentino, Italy.
Marco BazzicalupoDepartment of Biology, University of Florence, 50019 Sesto Fiorentino, Italy.
Alessio MengoniDepartment of Biology, University of Florence, 50019 Sesto Fiorentino, Italy.ORCID 0000-0002-1265-8251
Carlo VitiDepartment of Agri-food Production and Environmental Sciences, University of Florence, 50144 Sesto Fiorentino, Italy.
Lukasz DziewitDepartment of Bacterial Genetics, Institute of Microbiology, Faculty of Biology, University of Warsaw, 02-096 Warsaw, Poland.
Turlough M FinanDepartment of Biology, McMaster University, Hamilton, Ontario, Canada L8S 1A1.
Marco GalardiniEMBL-EBI, Wellcome Trust Genome Campus, Cambridge CB10 1SD, UK.ORCID 0000-0003-2018-8242
Marco FondiDepartment of Biology, University of Florence, 50019 Sesto Fiorentino, Italy.
University of Florence · ITMcMaster University · CAEuropean Bioinformatics Institute · GBUniversity of Warsaw · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genome of about 10% of bacterial species is divided among two or more large chromosome-sized replicons. The contribution of each replicon to the microbial life cycle (for example, environmental adaptations and/or niche switching) remains unclear. Here we report a genome-scale metabolic model of the legume symbiont Sinorhizobium meliloti that is integrated with carbon utilization data for 1,500 genes with 192 carbon substrates. Growth of S. meliloti is modelled in three ecological niches (bulk soil, rhizosphere and nodule) with a focus on the role of each of its three replicons. We observe clear metabolic differences during growth in the tested ecological niches and an overall reprogramming following niche switching. In silico examination of the inferred fitness of gene deletion mutants suggests that secondary replicons evolved to fulfil a specialized function, particularly host-associated niche adaptation. Thus, genes on secondary replicons might potentially be manipulated to promote or suppress host interactions for biotechnological purposes.

Indexed as

Adaptation, PhysiologicalEcosystemModels, BiologicalCarbonComputer SimulationGene DeletionGenetic FitnessGenome, BacterialMetabolic Networks and PathwaysPhenotypeRepliconReproducibility of ResultsRhizosphereSinorhizobium melilotiSoilSymbiosisCarbonSoil

Identifiers

PMID27447951
PMCPMC4961836
OpenAlexW2504092299

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.