Evidence map›Paper›PMID 27122562›Full record

ArticleProceedings. Biological sciences2016

Metapopulation dominance and genomic-island acquisition of Bradyrhizobium with superior catabolic capabilities.

Amanda C Hollowell, John U Regus, David Turissini, Kelsey A Gano-Cohen, Roxanne Bantay, Andrew Bernardo, Devora Moore, Jonathan Pham, Joel L Sachs

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings. Biological sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
9.6field-weighted citation impact, top 3% 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

10 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Widespread Distribution of Highly AdaptedFrontiers in microbiology · 2019
    Review
  8. Review
  9. Select and resequence reveals relative fitness of bacteria in symbiotic and free-living environments.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  10. Review
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 2 institutions in 1 country.

Amanda C HollowellDepartment of Biology, University of California, Riverside, CA 92521, USA.
John U RegusDepartment of Biology, University of California, Riverside, CA 92521, USA.
David TurissiniDepartment of Biology, University of North Carolina, Chapel Hill, NC 27599, USA.
Kelsey A Gano-CohenDepartment of Biology, University of California, Riverside, CA 92521, USA.
Roxanne BantayDepartment of Biology, University of California, Riverside, CA 92521, USA.
Andrew BernardoDepartment of Biology, University of California, Riverside, CA 92521, USA.
Devora MooreDepartment of Biology, University of California, Riverside, CA 92521, USA.
Jonathan PhamDepartment of Biology, University of California, Riverside, CA 92521, USA.
Joel L SachsDepartment of Biology, University of California, Riverside, CA 92521, USA Institute for Integrative Genome Biology, University of California, Riverside, CA 92521, USA joels@ucr.edu.
University of California, Riverside · USUniversity of North Carolina at Chapel Hill · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Root nodule-forming rhizobia exhibit a bipartite lifestyle, replicating in soil and also within plant cells where they fix nitrogen for legume hosts. Host control models posit that legume hosts act as a predominant selective force on rhizobia, but few studies have examined rhizobial fitness in natural populations. Here, we genotyped and phenotyped Bradyrhizobium isolates across more than 800 km of the native Acmispon strigosus host range. We sequenced chromosomal genes expressed under free-living conditions and accessory symbiosis loci expressed in planta and encoded on an integrated 'symbiosis island' (SI). We uncovered a massive clonal expansion restricted to the Bradyrhizobium chromosome, with a single chromosomal haplotype dominating populations, ranging more than 700 km, and acquiring 42 divergent SI haplotypes, none of which were spatially widespread. For focal genotypes, we quantified utilization of 190 sole-carbon sources relevant to soil fitness. Chromosomal haplotypes that were both widespread and dominant exhibited superior growth on diverse carbon sources, whereas these patterns were not mirrored among SI haplotypes. Abundance, spatial range and catabolic superiority of chromosomal, but not symbiosis genotypes suggests that fitness in the soil environment, rather than symbiosis with hosts, might be the key driver of Bradyrhizobium dominance.

Indexed as

Genomic IslandsBradyrhizobiumCarbon CycleEvolution, MolecularFabaceaeHaplotypesHost SpecificityLotusModels, GeneticPhylogenyRoot Nodules, PlantSoil MicrobiologySymbiosisepidemicfitnessgenomic islandrhizobiaselective sweepsymbiont

Identifiers

PMID27122562
PMCPMC4855393
OpenAlexW2343862577

What OpenQuestion holds

Textmetadata
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.