Evidence map›Paper›PMID 21811606›Full record

ArticlePloS one2011

Identification of the pangenome and its components in 14 distinct Aggregatibacter actinomycetemcomitans strains by comparative genomic analysis.

Weerayuth Kittichotirat, Roger E Bumgarner, Sirkka Asikainen, Casey Chen

Abstract readComparative Study
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing 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

56 citing papers in PubMed.

  1. Fimbriae potentiateCurrent research in microbial sciences · 2026
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  2. Pins Gene Table v2.0: An Online Genome Database of 37Journal of fungi (Basel, Switzerland) · 2024
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  9. Frontiers in oral health · 2022
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  11. Review
  12. Transcriptomic Analysis ofPathogens (Basel, Switzerland) · 2019
    Article
  13. Whole Genome Sequencing ofPathogens (Basel, Switzerland) · 2019
    Article
  14. Pathogens (Basel, Switzerland) · 2019
    Review
  15. Article
  16. Virulence and Pathogenicity Properties ofPathogens (Basel, Switzerland) · 2019
    Review
  17. Genetic Profiling ofPathogens (Basel, Switzerland) · 2019
    Article
  18. A Nonfimbrial Adhesin ofInfection and immunity · 2019
    Article
  19. Article
  20. Article
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

4 authors.

Weerayuth KittichotiratDepartment of Microbiology, University of Washington, Seattle, Washington, United States of America.
Roger E Bumgarner
Sirkka Asikainen
Casey Chen

Funding

Novel clone-specific virulence determinants of A. actinomycetemcomitansR01DE012212 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHEN, CASEY · 1999 to 2016
$5.0M
NIDCR NIH HHS R01 DE012212NIDCR NIH HHS R01 DE12212
6 · The paper itself

Abstract

backgroundAggregatibacter actinomycetemcomitans is genetically heterogeneous and comprises distinct clonal lineages that may have different virulence potentials. However, limited information of the strain-to-strain genomic variations is available. METHODOLOGY/PRINCIPAL

findingsThe genome sequences of 11 A. actinomycetemcomitans strains (serotypes a-f) were generated de novo, annotated and combined with three previously sequenced genomes (serotypes a-c) for comparative genomic analysis. Two major groups were identified; serotypes a, d, e, and f, and serotypes b and c. A serotype e strain was found to be distinct from both groups. The size of the pangenome was 3,301 genes, which included 2,034 core genes and 1,267 flexible genes. The number of core genes is estimated to stabilize at 2,060, while the size of the pangenome is estimated to increase by 16 genes with every additional strain sequenced in the future. Within each strain 16.7-29.4% of the genome belonged to the flexible gene pool. Between any two strains 0.4-19.5% of the genomes were different. The genomic differences were occasionally greater for strains of the same serotypes than strains of different serotypes. Furthermore, 171 genomic islands were identified. Cumulatively, 777 strain-specific genes were found on these islands and represented 61% of the flexible gene pool. CONCLUSIONS/SIGNIFICANCE: Substantial genomic differences were detected among A. actinomycetemcomitans strains. Genomic islands account for more than half of the flexible genes. The phenotype and virulence of A. actinomycetemcomitans may not be defined by any single strain. Moreover, the genomic variation within each clonal lineage of A. actinomycetemcomitans (as defined by serotype grouping) may be greater than between clonal lineages. The large genomic data set in this study will be useful to further examine the molecular basis of variable virulence among A. actinomycetemcomitans strains.

Indexed as

ActinobacillusCluster AnalysisComparative Genomic HybridizationGene PoolGenes, BacterialGenome, BacterialGenomic IslandsMolecular Sequence AnnotationPhylogenySequence Analysis, DNASpecies SpecificityVirulence

Identifiers

PMID21811606
PMCPMC3139650

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Registered trials

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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.