Evidence map›Paper›PMID 25794000›Full record

ArticlePloS one2015

Scanning the landscape of genome architecture of non-O1 and non-O139 Vibrio cholerae by whole genome mapping reveals extensive population genetic diversity.

Carol Chapman, Matthew Henry, Kimberly A Bishop-Lilly, Joy Awosika, Adam Briska, Ryan N Ptashkin, Trevor Wagner, Chythanya Rajanna, Hsinyi Tsang, Shannon L Johnson and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Microbial genomics · 2023
    Article
  4. Review
  5. Article
  6. Zebrafish Models for Pathogenic Vibrios.Journal of bacteriology · 2020
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Functionality of Two Origins of Replication inFrontiers in microbiology · 2018
    Article
  12. Review
  13. Article
  14. Article
  15. 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

13 authors at 6 institutions in 1 country.

Carol ChapmanHenry M. Jackson Foundation, Bethesda, Maryland, United States of America; Naval Medical Research Center-Frederick, Fort Detrick, Maryland, United States of America.
Matthew HenryHenry M. Jackson Foundation, Bethesda, Maryland, United States of America; Naval Medical Research Center-Frederick, Fort Detrick, Maryland, United States of America.
Kimberly A Bishop-LillyHenry M. Jackson Foundation, Bethesda, Maryland, United States of America; Naval Medical Research Center-Frederick, Fort Detrick, Maryland, United States of America.
Joy AwosikaHenry M. Jackson Foundation, Bethesda, Maryland, United States of America; Naval Medical Research Center-Frederick, Fort Detrick, Maryland, United States of America.
Adam BriskaOpGen, Inc., Gaithersburg, Maryland, United States of America.
Ryan N PtashkinOpGen, Inc., Gaithersburg, Maryland, United States of America.
Trevor WagnerOpGen, Inc., Gaithersburg, Maryland, United States of America.
Chythanya RajannaUniversity of Florida, Gainesville, Florida, United States of America.
Hsinyi TsangHenry M. Jackson Foundation, Bethesda, Maryland, United States of America; Naval Medical Research Center-Frederick, Fort Detrick, Maryland, United States of America.
Shannon L JohnsonGenome Science, Biosciences Division, Los Alamos National Laboratory, Los Alamos, New Mexico, United States of America.
Vishwesh P MokashiNaval Medical Research Center-Frederick, Fort Detrick, Maryland, United States of America.
Patrick S G ChainGenome Science, Biosciences Division, Los Alamos National Laboratory, Los Alamos, New Mexico, United States of America.
Shanmuga SozhamannanHenry M. Jackson Foundation, Bethesda, Maryland, United States of America; Naval Medical Research Center-Frederick, Fort Detrick, Maryland, United States of America.
Henry M. Jackson Foundation · USOpGen (United States) · USJackson Foundation · USLos Alamos National Laboratory · USNaval Medical Research Command · USUniversity of Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Historically, cholera outbreaks have been linked to V. cholerae O1 serogroup strains or its derivatives of the O37 and O139 serogroups. A genomic study on the 2010 Haiti cholera outbreak strains highlighted the putative role of non O1/non-O139 V. cholerae in causing cholera and the lack of genomic sequences of such strains from around the world. Here we address these gaps by scanning a global collection of V. cholerae strains as a first step towards understanding the population genetic diversity and epidemic potential of non O1/non-O139 strains. Whole Genome Mapping (Optical Mapping) based bar coding produces a high resolution, ordered restriction map, depicting a complete view of the unique chromosomal architecture of an organism. To assess the genomic diversity of non-O1/non-O139 V. cholerae, we applied a Whole Genome Mapping strategy on a well-defined and geographically and temporally diverse strain collection, the Sakazaki serogroup type strains. Whole Genome Map data on 91 of the 206 serogroup type strains support the hypothesis that V. cholerae has an unprecedented genetic and genomic structural diversity. Interestingly, we discovered chromosomal fusions in two unusual strains that possess a single chromosome instead of the two chromosomes usually found in V. cholerae. We also found pervasive chromosomal rearrangements such as duplications and indels in many strains. The majority of Vibrio genome sequences currently in public databases are unfinished draft sequences. The Whole Genome Mapping approach presented here enables rapid screening of large strain collections to capture genomic complexities that would not have been otherwise revealed by unfinished draft genome sequencing and thus aids in assembling and finishing draft sequences of complex genomes. Furthermore, Whole Genome Mapping allows for prediction of novel V. cholerae non-O1/non-O139 strains that may have the potential to cause future cholera outbreaks.

Indexed as

Genetic VariationGenome, BacterialChromosome MappingChromosomes, BacterialDNA, BacterialElectrophoresis, Gel, Pulsed-FieldGene DuplicationGene RearrangementGenome SizeINDEL MutationPhylogenyReproducibility of ResultsRestriction MappingSequence Analysis, DNAVibrio choleraeDNA, Bacterial

Identifiers

PMID25794000
PMCPMC4368569
OpenAlexW1984804812

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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.