Evidence map›Paper›PMID 27014193›Full record

ArticleFrontiers in microbiology2016

Why Close a Bacterial Genome? The Plasmid of Alteromonas Macleodii HOT1A3 is a Vector for Inter-Specific Transfer of a Flexible Genomic Island.

Eduard Fadeev, Fabio De Pascale, Alessandro Vezzi, Sariel Hübner, Dikla Aharonovich, Daniel Sher

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2016. 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
–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

18 citing papers in PubMed.

  1. Journal of biosciences · 2026
    Article
  2. Article
  3. Article
  4. Elucidating the genomic history of commercially usedFrontiers in cellular and infection microbiology · 2023
    Article
  5. Article
  6. Review
  7. Comparative Genomics ofMicroorganisms · 2020
    Article
  8. mBio · 2020
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. 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

6 authors.

Eduard FadeevDepartment of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa Haifa, Israel.
Fabio De PascaleDepartment of Biology and CRIBI Biotechnology Centre, University of Padua Padova, Italy.
Alessandro VezziDepartment of Biology and CRIBI Biotechnology Centre, University of Padua Padova, Italy.
Sariel HübnerDepartment of Botany and Biodiversity Research Centre, University of British ColumbiaVancouver, Canada; The Department of Evolutionary and Environmental Biology, University of HaifaHaifa, Israel.
Dikla AharonovichDepartment of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa Haifa, Israel.
Daniel SherDepartment of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa Haifa, Israel.

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
NCATS NIH HHS UL1 TR001863
6 · The paper itself

Abstract

Genome sequencing is rapidly becoming a staple technique in environmental and clinical microbiology, yet computational challenges still remain, leading to many draft genomes which are typically fragmented into many contigs. We sequenced and completely assembled the genome of a marine heterotrophic bacterium, Alteromonas macleodii HOT1A3, and compared its full genome to several draft genomes obtained using different reference-based and de novo methods. In general, the de novo assemblies clearly outperformed the reference-based or hybrid ones, covering >99% of the genes and representing essentially all of the gene functions. However, only the fully closed genome (∼4.5 Mbp) allowed us to identify the presence of a large, 148 kbp plasmid, pAM1A3. While HOT1A3 belongs to A. macleodii, typically found in surface waters ("surface ecotype"), this plasmid consists of an almost complete flexible genomic island (fGI), containing many genes involved in metal resistance previously identified in the genomes of Alteromonas mediterranea ("deep ecotype"). Indeed, similar to A. mediterranea, A. macleodii HOT1A3 grows at concentrations of zinc, mercury, and copper that are inhibitory for other A. macleodii strains. The presence of a plasmid encoding almost an entire fGI suggests that wholesale genomic exchange between heterotrophic marine bacteria belonging to related but ecologically different populations is not uncommon.

Indexed as

Alteromonasgenome assemblygenomic islandmetal resistanceplasmid

Identifiers

PMID27014193
PMCPMC4781885

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.