Evidence map›Paper›PMID 21602358›Full record

ArticleJournal of bacteriology2011

Comparative genomics of 28 Salmonella enterica isolates: evidence for CRISPR-mediated adaptive sublineage evolution.

W Florian Fricke, Mark K Mammel, Patrick F McDermott, Carmen Tartera, David G White, J Eugene Leclerc, Jacques Ravel, Thomas A Cebula

Abstract readComparative Study
In one paragraph

Article in Journal of bacteriology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
31.8field-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

85 citing papers in PubMed, 162 citations in OpenAlex.

  1. Pathogens (Basel, Switzerland) · 2026
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  5. Genomic Insights into the Pathogenicity of HypervirulentPathogens (Basel, Switzerland) · 2025
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  6. Transcriptomic Analysis ofInternational journal of molecular sciences · 2025
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  7. Genotypes and associated traits inFrontiers in microbiology · 2025
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  15. Article
  16. Review
  17. Article
  18. Comparative Genomics ofFrontiers in microbiology · 2020
    Article
  19. Article
  20. Article

25 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

8 authors at 4 institutions in 1 country.

W Florian FrickeInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA. wffricke@som.umaryland.edu
Mark K Mammel
Patrick F McDermott
Carmen Tartera
David G White
J Eugene Leclerc
Jacques Ravel
Thomas A Cebula
Center for Food Safety and Applied Nutrition · USCenter for Veterinary Medicine · USUniversity of Maryland, Baltimore · USJohns Hopkins University · US

Funding

NIAID NIH HHS N01 AI030071
6 · The paper itself

Abstract

Despite extensive surveillance, food-borne Salmonella enterica infections continue to be a significant burden on public health systems worldwide. As the S. enterica species comprises sublineages that differ greatly in antigenic representation, virulence, and antimicrobial resistance phenotypes, a better understanding of the species' evolution is critical for the prediction and prevention of future outbreaks. The roles that virulence and resistance phenotype acquisition, exchange, and loss play in the evolution of S. enterica sublineages, which to a certain extent are represented by serotypes, remains mostly uncharacterized. Here, we compare 17 newly sequenced and phenotypically characterized nontyphoidal S. enterica strains to 11 previously sequenced S. enterica genomes to carry out the most comprehensive comparative analysis of this species so far. These phenotypic and genotypic data comparisons in the phylogenetic species context suggest that the evolution of known S. enterica sublineages is mediated mostly by two mechanisms, (i) the loss of coding sequences with known metabolic functions, which leads to functional reduction, and (ii) the acquisition of horizontally transferred phage and plasmid DNA, which provides virulence and resistance functions and leads to increasing specialization. Matches between S. enterica clustered regularly interspaced short palindromic repeats (CRISPR), part of a defense mechanism against invading plasmid and phage DNA, and plasmid and prophage regions suggest that CRISPR-mediated immunity could control short-term phenotype changes and mediate long-term sublineage evolution. CRISPR analysis could therefore be critical in assessing the evolutionary potential of S. enterica sublineages and aid in the prediction and prevention of future S. enterica outbreaks.

Indexed as

Evolution, MolecularGenomicsInverted Repeat SequencesGenome, BacterialHumansPhylogenySalmonella entericaSalmonella Infections

Identifiers

PMID21602358
PMCPMC3133335
OpenAlexW2081209254

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.