Evidence map›Paper›PMID 25313016›Full record

ArticleGenome biology and evolution2014

The genomic diversification of the whole Acinetobacter genus: origins, mechanisms, and consequences.

Marie Touchon, Jean Cury, Eun-Jeong Yoon, Lenka Krizova, Gustavo C Cerqueira, Cheryl Murphy, Michael Feldgarden, Jennifer Wortman, Dominique Clermont, Thierry Lambert and 4 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 151 papers.

0numbers the graph read from it
0cells of the map it votes in
151citing papers in PubMed
9.2field-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

151 citing papers in PubMed, 274 citations in OpenAlex.

  1. Article
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  3. Foods (Basel, Switzerland) · 2026
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  5. Comparative genomic analysis ofJAC-antimicrobial resistance · 2026
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  6. Redefining Antimicrobial Resistance inInternational journal of molecular sciences · 2026
    Review
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  10. Microbial genomics · 2026
    Article
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  12. History of the taxonomy ofInternational journal of systematic and evolutionary microbiology · 2025
    Article
  13. Phage Therapy forAntibiotics (Basel, Switzerland) · 2025
    Review
  14. Distinct codon usage signatures reflecting evolutionary and pathogenic adaptation in the Acinetobacter baumannii complex.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Exploring the Multifaceted GenusJournal of microbiology and biotechnology · 2025
    Review

91 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

14 authors at 4 institutions in 3 countries.

Marie TouchonMicrobial Evolutionary Genomics, Institut Pasteur, Paris, France CNRS, UMR3525, Paris, France.
Jean CuryMicrobial Evolutionary Genomics, Institut Pasteur, Paris, France CNRS, UMR3525, Paris, France.
Eun-Jeong YoonUnité des Agents Antibactériens, Institut Pasteur, Paris, France.
Lenka KrizovaLaboratory of Bacterial Genetics, National Institute of Public Health, Prague, Czech Republic.
Gustavo C CerqueiraBroad Institute of Harvard and MIT, Cambridge, Massachusetts.
Cheryl MurphyBroad Institute of Harvard and MIT, Cambridge, Massachusetts.
Michael FeldgardenBroad Institute of Harvard and MIT, Cambridge, Massachusetts.
Jennifer WortmanBroad Institute of Harvard and MIT, Cambridge, Massachusetts.
Dominique ClermontCollection de l'Institut Pasteur, Institut Pasteur, Paris, France.
Thierry LambertUnité des Agents Antibactériens, Institut Pasteur, Paris, France.
Catherine Grillot-CourvalinUnité des Agents Antibactériens, Institut Pasteur, Paris, France.
Alexandr NemecLaboratory of Bacterial Genetics, National Institute of Public Health, Prague, Czech Republic. anemec@szu.cz patrice.courvalin@pasteur.fr erocha@pasteur.fr.
Patrice CourvalinUnité des Agents Antibactériens, Institut Pasteur, Paris, France anemec@szu.cz patrice.courvalin@pasteur.fr erocha@pasteur.fr.
Eduardo P C RochaMicrobial Evolutionary Genomics, Institut Pasteur, Paris, France CNRS, UMR3525, Paris, France anemec@szu.cz patrice.courvalin@pasteur.fr erocha@pasteur.fr.
Institut Pasteur · FRBroad Institute · USCentre National de la Recherche Scientifique · FRNational Institute of Public Health · CZ

Funding

Viral Genomics: evolution, spread, and host interactionsU19AI110818 · NIAID · BROAD INSTITUTE, INC. · PI CUOMO, CHRISTINA A · 2014 to 2024
$66.5M
NIAID NIH HHS HHSN272200900018CNIAID NIH HHS U19 AI110818
6 · The paper itself

Abstract

Bacterial genomics has greatly expanded our understanding of microdiversification patterns within a species, but analyses at higher taxonomical levels are necessary to understand and predict the independent rise of pathogens in a genus. We have sampled, sequenced, and assessed the diversity of genomes of validly named and tentative species of the Acinetobacter genus, a clade including major nosocomial pathogens and biotechnologically important species. We inferred a robust global phylogeny and delimited several new putative species. The genus is very ancient and extremely diverse: Genomes of highly divergent species share more orthologs than certain strains within a species. We systematically characterized elements and mechanisms driving genome diversification, such as conjugative elements, insertion sequences, and natural transformation. We found many error-prone polymerases that may play a role in resistance to toxins, antibiotics, and in the generation of genetic variation. Surprisingly, temperate phages, poorly studied in Acinetobacter, were found to account for a significant fraction of most genomes. Accordingly, many genomes encode clustered regularly interspaced short palindromic repeats (CRISPR)-Cas systems with some of the largest CRISPR-arrays found so far in bacteria. Integrons are strongly overrepresented in Acinetobacter baumannii, which correlates with its frequent resistance to antibiotics. Our data suggest that A. baumannii arose from an ancient population bottleneck followed by population expansion under strong purifying selection. The outstanding diversification of the species occurred largely by horizontal transfer, including some allelic recombination, at specific hotspots preferentially located close to the replication terminus. Our work sets a quantitative basis to understand the diversification of Acinetobacter into emerging resistant and versatile pathogens.

Indexed as

AcinetobacterClustered Regularly Interspaced Short Palindromic RepeatsGenome, BacterialGenomicsInterspersed Repetitive SequencesPhylogenybacterial genuscomparative genomicsevolutionmobile genetic elementsnosocomial pathogens

Identifiers

PMID25313016
PMCPMC4224351
OpenAlexW2136309448

What OpenQuestion holds

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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.