Evidence map›Paper›PMID 23365658›Full record

ArticlePloS one2013

Evolution of a pathogen: a comparative genomics analysis identifies a genetic pathway to pathogenesis in Acinetobacter.

Jason W Sahl, John D Gillece, James M Schupp, Victor G Waddell, Elizabeth M Driebe, David M Engelthaler, Paul Keim

Abstract readComparative Study
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
–field-weighted citation impact
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

82 citing papers in PubMed.

  1. Article
  2. Bacteriophages targetingFrontiers in microbiology · 2026
    Review
  3. Article
  4. History of the taxonomy ofInternational journal of systematic and evolutionary microbiology · 2025
    Article
  5. Article
  6. mBio · 2024
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Genomic Investigation of TwoPathogens (Basel, Switzerland) · 2022
    Article
  13. Article
  14. Article
  15. Pan-Resistome Insights into the Multidrug Resistance ofAntibiotics (Basel, Switzerland) · 2021
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

22 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

7 authors.

Jason W SahlDepartment of Pathogen Genomics, Translational Genomics Research Institute, Flagstaff, Arizona, United States of America. jsahl@tgen.org
John D Gillece
James M Schupp
Victor G Waddell
Elizabeth M Driebe
David M Engelthaler
Paul Keim

Funding

Molecular Antibiotic Resistance Arrays for clinical microbiology laboratoriesR01AI090782 · NIAID · TRANSLATIONAL GENOMICS RESEARCH INST · PI KEIM, PAUL STEPHEN · 2010 to 2014
$4.6M
NIAID NIH HHS R01 AI090782NIAID NIH HHS R01AI090782-03
6 · The paper itself

Abstract

Acinetobacter baumannii is an emergent and global nosocomial pathogen. In addition to A. baumannii, other Acinetobacter species, especially those in the Acinetobacter calcoaceticus-baumannii (Acb) complex, have also been associated with serious human infection. Although mechanisms of attachment, persistence on abiotic surfaces, and pathogenesis in A. baumannii have been identified, the genetic mechanisms that explain the emergence of A. baumannii as the most widespread and virulent Acinetobacter species are not fully understood. Recent whole genome sequencing has provided insight into the phylogenetic structure of the genus Acinetobacter. However, a global comparison of genomic features between Acinetobacter spp. has not been described in the literature. In this study, 136 Acinetobacter genomes, including 67 sequenced in this study, were compared to identify the acquisition and loss of genes in the expansion of the Acinetobacter genus. A whole genome phylogeny confirmed that A. baumannii is a monophyletic clade and that the larger Acb complex is also a well-supported monophyletic group. The whole genome phylogeny provided the framework for a global genomic comparison based on a blast score ratio (BSR) analysis. The BSR analysis demonstrated that specific genes have been both lost and acquired in the evolution of A. baumannii. In addition, several genes associated with A. baumannii pathogenesis were found to be more conserved in the Acb complex, and especially in A. baumannii, than in other Acinetobacter genomes; until recently, a global analysis of the distribution and conservation of virulence factors across the genus was not possible. The results demonstrate that the acquisition of specific virulence factors has likely contributed to the widespread persistence and virulence of A. baumannii. The identification of novel features associated with transcriptional regulation and acquired by clades in the Acb complex presents targets for better understanding the evolution of pathogenesis and virulence in the expansion of the genus.

Indexed as

Genome, BacterialAcinetobacterAcinetobacter baumanniiAcinetobacter InfectionsBacterial ProteinsBase SequenceBiological EvolutionChromosome MappingChromosomes, BacterialGenomicsHumansMultilocus Sequence TypingPhylogenyRNA, Ribosomal, 16SVirulenceVirulence FactorsBacterial ProteinsRNA, Ribosomal, 16SVirulence Factors

Identifiers

PMID23365658
PMCPMC3554770

What OpenQuestion holds

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LicenceCC BY
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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.