Evidence map›Paper›PMID 25058595›Full record

ArticlePloS one2014

The expanded diversity of methylophilaceae from Lake Washington through cultivation and genomic sequencing of novel ecotypes.

David A C Beck, Tami L McTaggart, Usanisa Setboonsarng, Alexey Vorobev, Marina G Kalyuzhnaya, Natalia Ivanova, Lynne Goodwin, Tanja Woyke, Mary E Lidstrom, Ludmila Chistoserdova

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

34 citing papers in PubMed, 82 citations in OpenAlex.

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  19. Lanthanide-dependent cross-feeding of methane-derived carbon is linked by microbial community interactions.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
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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

10 authors at 3 institutions in 1 country.

David A C BeckDepartment of Chemical Engineering, University of Washington, Seattle, Washington, United States of America; eScience Institute, University of Washington, Seattle, Washington, United States of America.
Tami L McTaggartDepartment of Chemical Engineering, University of Washington, Seattle, Washington, United States of America.
Usanisa SetboonsarngDepartment of Chemical Engineering, University of Washington, Seattle, Washington, United States of America.
Alexey VorobevDepartment of Chemical Engineering, University of Washington, Seattle, Washington, United States of America.
Marina G KalyuzhnayaDepartment of Microbiology, University of Washington, Seattle, Washington, United States of America.
Natalia IvanovaDOE Joint Genome Institute, Walnut Creek, California, United States of America.
Lynne GoodwinLos Alamos National Laboratory, Los Alamos, New Mexico, United States of America.
Tanja WoykeDOE Joint Genome Institute, Walnut Creek, California, United States of America.
Mary E LidstromDepartment of Chemical Engineering, University of Washington, Seattle, Washington, United States of America; Department of Microbiology, University of Washington, Seattle, Washington, United States of America.
Ludmila ChistoserdovaDepartment of Chemical Engineering, University of Washington, Seattle, Washington, United States of America.
University of Washington · USJoint Genome Institute · USLos Alamos National Laboratory · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We describe five novel Methylophilaceae ecotypes from a single ecological niche in Lake Washington, USA, and compare them to three previously described ecotypes, in terms of their phenotype and genome sequence divergence. Two of the ecotypes appear to represent novel genera within the Methylophilaceae. Genome-based metabolic reconstruction highlights metabolic versatility of Methylophilaceae with respect to methylotrophy and nitrogen metabolism, different ecotypes possessing different combinations of primary substrate oxidation systems (MxaFI-type methanol dehydrogenase versus XoxF-type methanol dehydrogenase; methylamine dehydrogenase versus N-methylglutamate pathway) and different potentials for denitrification (assimilatory versus respiratory nitrate reduction). By comparing pairs of closely related genomes, we uncover that site-specific recombination is the main means of genomic evolution and strain divergence, including lateral transfers of genes from both closely- and distantly related taxa. The new ecotypes and the new genomes contribute significantly to our understanding of the extent of genomic and metabolic diversity among organisms of the same family inhabiting the same ecological niche. These organisms also provide novel experimental models for studying the complexity and the function of the microbial communities active in methylotrophy.

Indexed as

Genome, BacterialPhylogenyAlcohol OxidoreductasesBacterial ProteinsDenitrificationEcotypeGenetic VariationGlutamatesLakesMethylophilaceaeNitrogenOxidoreductases Acting on CH-NH Group DonorsRecombination, GeneticWashingtonalcohol dehydrogenase (acceptor)Alcohol OxidoreductasesBacterial ProteinsGlutamatesmethylamine dehydrogenaseNitrogenN-methylglutamateOxidoreductases Acting on CH-NH Group Donors

Identifiers

PMID25058595
PMCPMC4109929
OpenAlexW2059701046

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.