Evidence map›Paper›PMID 32393168›Full record

ArticleBMC genomics2020

Genomic variation among closely related Vibrio alginolyticus strains is located on mobile genetic elements.

Cynthia Maria Chibani, Olivia Roth, Heiko Liesegang, Carolin Charlotte Wendling

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.0field-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

18 citing papers in PubMed, 32 citations in OpenAlex.

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  11. Phylogenomic diversity ofMicrobial genomics · 2022
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  14. Comparative Genomic Analysis ofInternational journal of molecular sciences · 2022
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  15. Comparative Genomic Analysis of SevenFrontiers in microbiology · 2022
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  16. Article
  17. Article
  18. Closely RelatedViruses · 2020
    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

4 authors at 2 institutions in 2 countries.

Cynthia Maria ChibaniDepartment of Genomic and Applied Microbiology, Institute of Microbiology and Genetics, Georg-August-University, 37077, Göttingen, Germany.
Olivia RothGEOMAR, Helmholtz Centre for Ocean Research, Marine Evolutionary Ecology, Duesternbrooker Weg 20, 24105, Kiel, Germany.
Heiko LiesegangDepartment of Genomic and Applied Microbiology, Institute of Microbiology and Genetics, Georg-August-University, 37077, Göttingen, Germany.
Carolin Charlotte WendlingGEOMAR, Helmholtz Centre for Ocean Research, Marine Evolutionary Ecology, Duesternbrooker Weg 20, 24105, Kiel, Germany. carolin.wendling@env.ethz.ch.ORCID http://orcid.org/0000-0003-4532-7528
GEOMAR Helmholtz Centre for Ocean Research Kiel · DEUniversity of Göttingen · DE

Funding

Deutsche Forschungsgemeinschaft RO462/4-2Deutsche Forschungsgemeinschaft WE 5822/ 1-1Deutsche Forschungsgemeinschaft WE5822/1-2KAAD na
6 · The paper itself

Abstract

backgroundSpecies of the genus Vibrio, one of the most diverse bacteria genera, have undergone niche adaptation followed by clonal expansion. Niche adaptation and ultimately the formation of ecotypes and speciation in this genus has been suggested to be mainly driven by horizontal gene transfer (HGT) through mobile genetic elements (MGEs). Our knowledge about the diversity and distribution of Vibrio MGEs is heavily biased towards human pathogens and our understanding of the distribution of core genomic signatures and accessory genes encoded on MGEs within specific Vibrio clades is still incomplete. We used nine different strains of the marine bacterium Vibrio alginolyticus isolated from pipefish in the Kiel-Fjord to perform a multiscale-comparative genomic approach that allowed us to investigate [1] those genomic signatures that characterize a habitat-specific ecotype and [2] the source of genomic variation within this ecotype.

resultsWe found that the nine isolates from the Kiel-Fjord have a closed-pangenome and did not differ based on core-genomic signatures. Unique genomic regions and a unique repertoire of MGEs within the Kiel-Fjord isolates suggest that the acquisition of gene-blocks by HGT played an important role in the evolution of this ecotype. Additionally, we found that ~ 90% of the genomic variation among the nine isolates is encoded on MGEs, which supports ongoing theory that accessory genes are predominately located on MGEs and shared by HGT. Lastly, we could show that these nine isolates share a unique virulence and resistance profile which clearly separates them from all other investigated V. alginolyticus strains and suggests that these are habitat-specific genes, required for a successful colonization of the pipefish, the niche of this ecotype.

conclusionWe conclude that all nine V. alginolyticus strains from the Kiel-Fjord belong to a unique ecotype, which we named the Kiel-alginolyticus ecotype. The low sequence variation of the core-genome in combination with the presence of MGE encoded relevant traits, as well as the presence of a suitable niche (here the pipefish), suggest, that this ecotype might have evolved from a clonal expansion following HGT driven niche-adaptation.

Indexed as

Genetic VariationGenome, BacterialDrug ResistanceEvolution, MolecularGene Transfer, HorizontalGenomic IslandsPhylogenyVibrio alginolyticusVirulenceGenomic islandsHorizontal gene transferMega-plasmidsMobile genetic elementsNiche-adaptationPangenome

Identifiers

PMID32393168
PMCPMC7216594
OpenAlexW3026401758

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LicenceCC BY
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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.