Evidence map›Paper›PMID 25848870›Full record

ArticleThe ISME journal2015

Rapid selective sweep of pre-existing polymorphisms and slow fixation of new mutations in experimental evolution of Desulfovibrio vulgaris.

Aifen Zhou, Kristina L Hillesland, Zhili He, Wendy Schackwitz, Qichao Tu, Grant M Zane, Qiao Ma, Yuanyuan Qu, David A Stahl, Judy D Wall and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The ISME journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

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  12. Stochastic Community Assembly: Does It Matter in Microbial Ecology?Microbiology and molecular biology reviews : MMBR · 2017
    Review
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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

14 authors at 9 institutions in 2 countries.

Aifen ZhouInstitute for Environmental Genomics, Department of Microbiology and Plant Biology, University of Oklahoma, Norman, OK, USA.
Kristina L HilleslandBiological Sciences, University of Washington Bothell, Bothell, WA, USA.
Zhili HeInstitute for Environmental Genomics, Department of Microbiology and Plant Biology, University of Oklahoma, Norman, OK, USA.
Wendy SchackwitzDepartment of Energy Joint Genome Institute, Walnut Creek, CA, USA.
Qichao TuInstitute for Environmental Genomics, Department of Microbiology and Plant Biology, University of Oklahoma, Norman, OK, USA.
Grant M ZaneDepartments of Biochemistry and Molecular Microbiology and Immunology, University of Missouri-Columbia, Columbia, MO, USA.
Qiao MaInstitute for Environmental Genomics, Department of Microbiology and Plant Biology, University of Oklahoma, Norman, OK, USA.
Yuanyuan QuInstitute for Environmental Genomics, Department of Microbiology and Plant Biology, University of Oklahoma, Norman, OK, USA.
David A StahlCivil and Environmental Engineering, University of Washington, Seattle, WA, USA.
Judy D WallDepartments of Biochemistry and Molecular Microbiology and Immunology, University of Missouri-Columbia, Columbia, MO, USA.
Terry C HazenDepartment of Civil and Environmental Engineering, The University of Tennessee, Knoxville, TN, USA.
Matthew W FieldsDepartment of Microbiology and Immunology, Montana State University, Bozeman, MT, USA.
Adam P ArkinPhysical Biosciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
Jizhong ZhouInstitute for Environmental Genomics, Department of Microbiology and Plant Biology, University of Oklahoma, Norman, OK, USA.
University of Oklahoma · USUniversity of Missouri · USDalian University of Technology · CNJoint Genome Institute · USLawrence Berkeley National Laboratory · USMontana State University · USOak Ridge National Laboratory · USUniversity of Washington · USUniversity of Washington Bothell · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To investigate the genetic basis of microbial evolutionary adaptation to salt (NaCl) stress, populations of Desulfovibrio vulgaris Hildenborough (DvH), a sulfate-reducing bacterium important for the biogeochemical cycling of sulfur, carbon and nitrogen, and potentially the bioremediation of toxic heavy metals and radionuclides, were propagated under salt stress or non-stress conditions for 1200 generations. Whole-genome sequencing revealed 11 mutations in salt stress-evolved clone ES9-11 and 14 mutations in non-stress-evolved clone EC3-10. Whole-population sequencing data suggested the rapid selective sweep of the pre-existing polymorphisms under salt stress within the first 100 generations and the slow fixation of new mutations. Population genotyping data demonstrated that the rapid selective sweep of pre-existing polymorphisms was common in salt stress-evolved populations. In contrast, the selection of pre-existing polymorphisms was largely random in EC populations. Consistently, at 100 generations, stress-evolved population ES9 showed improved salt tolerance, namely increased growth rate (2.0-fold), higher biomass yield (1.8-fold) and shorter lag phase (0.7-fold) under higher salinity conditions. The beneficial nature of several mutations was confirmed by site-directed mutagenesis. All four tested mutations contributed to the shortened lag phases under higher salinity condition. In particular, compared with the salt tolerance improvement in ES9-11, a mutation in a histidine kinase protein gene lytS contributed 27% of the growth rate increase and 23% of the biomass yield increase while a mutation in hypothetical gene DVU2472 contributed 24% of the biomass yield increase. Our results suggested that a few beneficial mutations could lead to dramatic improvements in salt tolerance.

Indexed as

Evolution, MolecularMutationPolymorphism, GeneticAdaptation, PhysiologicalBiodegradation, EnvironmentalBiomassDesulfovibrio vulgarisDNA Mutational AnalysisGene FrequencyGenotypeMetals, HeavyMutagenesis, Site-DirectedPhenotypeSalinitySalt ToleranceSodium ChlorideMetals, HeavySodium ChlorideSulfur

Identifiers

PMID25848870
PMCPMC4611501
OpenAlexW2323117146

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.