Evidence map›Paper›PMID 19720995›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

Comparative genomics reveals mechanism for short-term and long-term clonal transitions in pandemic Vibrio cholerae.

Jongsik Chun, Christopher J Grim, Nur A Hasan, Je Hee Lee, Seon Young Choi, Bradd J Haley, Elisa Taviani, Yoon-Seong Jeon, Dong Wook Kim, Jae-Hak Lee and 13 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 231 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
231citing papers in PubMed, 1 pooled it
20.4field-weighted citation impact, top 1% 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

231 citing papers in PubMed, 1 synthesis or guideline pooled it, 377 citations in OpenAlex.

  1. Pooled it
  2. Genomic and epidemiological insights into a non-toxigenic Vibrio cholerae O1 Ogawa from an autochthonous case in Brazil.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Genome-wide investigation of outbreak-associatedFrontiers in microbiology · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Defence systems encoded by core genomic islands of seventh pandemicPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  13. Lineage-specific defence systems of pandemicPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  14. Article
  15. Article
  16. Allelic variations and gene cluster modularity act as nonlinear bottlenecks for cholera emergence.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  17. Exploring Mobile Genetic Elements in Vibrio cholerae.Genome biology and evolution · 2025
    Article
  18. mSphere · 2025
    Article
  19. Genomic characterization ofFrontiers in microbiology · 2025
    Article
  20. Whole genome sequence and comparative genomic analysis of novel Rickettsia koreansis strain CNH17-7 isolated from human.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2024
    Article

171 more citing papers are in PubMed but not listed here.

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

23 authors at 10 institutions in 4 countries.

Jongsik ChunSchool of Biological Sciences and Institute of Microbiology, Seoul National University, Seoul 151-742, Republic of Korea.
Christopher J Grim
Nur A Hasan
Je Hee Lee
Seon Young Choi
Bradd J Haley
Elisa Taviani
Yoon-Seong Jeon
Dong Wook Kim
Jae-Hak Lee
Thomas S Brettin
David C Bruce
Jean F Challacombe
J Chris Detter
Cliff S Han
A Christine Munk
Olga Chertkov
Linda Meincke
Elizabeth Saunders
Ronald A Walters
Anwar Huq
G Balakrish Nair
Rita R Colwell
Joint Genome Institute · USInternational Vaccine Institute · KRLos Alamos National Laboratory · USSeoul National University · KRUniversity of Maryland, College Park · USInternational Centre for Diarrhoeal Disease Research · BDJohns Hopkins University · USNational Institute of Cholera and Enteric Diseases · INPacific Northwest National Laboratory · USResearch Institute for Advanced Computer Science · US

Funding

MULTIVALENT AAV VECTORS FOR HIV-1 GENE THERAPYR01AI040001 · NIAID · CITY OF HOPE NATIONAL MEDICAL CENTER · PI CHATTERJEE, SASWATI · 1996 to 1998
–
NIAID NIH HHS N01 AI040001NIAID NIH HHS N01-AI-30001NIAID NIH HHS N01-AI-40001PHS HHS 1R01A139129-01
6 · The paper itself

Abstract

Vibrio cholerae, the causative agent of cholera, is a bacterium autochthonous to the aquatic environment, and a serious public health threat. V. cholerae serogroup O1 is responsible for the previous two cholera pandemics, in which classical and El Tor biotypes were dominant in the sixth and the current seventh pandemics, respectively. Cholera researchers continually face newly emerging and reemerging pathogenic clones carrying diverse combinations of phenotypic and genotypic properties, which significantly hampered control of the disease. To elucidate evolutionary mechanisms governing genetic diversity of pandemic V. cholerae, we compared the genome sequences of 23 V. cholerae strains isolated from a variety of sources over the past 98 years. The genome-based phylogeny revealed 12 distinct V. cholerae lineages, of which one comprises both O1 classical and El Tor biotypes. All seventh pandemic clones share nearly identical gene content. Using analogy to influenza virology, we define the transition from sixth to seventh pandemic strains as a "shift" between pathogenic clones belonging to the same O1 serogroup, but from significantly different phyletic lineages. In contrast, transition among clones during the present pandemic period is characterized as a "drift" between clones, differentiated mainly by varying composition of laterally transferred genomic islands, resulting in emergence of variants, exemplified by V. cholerae O139 and V. cholerae O1 El Tor hybrid clones. Based on the comparative genomics it is concluded that V. cholerae undergoes extensive genetic recombination via lateral gene transfer, and, therefore, genome assortment, not serogroup, should be used to define pathogenic V. cholerae clones.

Indexed as

Evolution, MolecularGenetic VariationPhylogenyBase SequenceCholera ToxinCluster AnalysisGene Transfer, HorizontalGenomic IslandsGenomicsMolecular Sequence DataSequence Analysis, DNASpecies SpecificityVibrio cholerae O1Cholera Toxin

Identifiers

PMID19720995
PMCPMC2741270
OpenAlexW1997337736

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.