Evidence map›Paper›PMID 22355013›Full record

ArticleMolecular biology and evolution2012

Phylogeny of Shiga toxin-producing Escherichia coli O157 isolated from cattle and clinically ill humans.

James L Bono, Timothy P L Smith, James E Keen, Gregory P Harhay, Tara G McDaneld, Robert E Mandrell, Woo Kyung Jung, Thomas E Besser, Peter Gerner-Smidt, Martina Bielaszewska and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology and evolution, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

23 citing papers in PubMed, 54 citations in OpenAlex.

  1. Frontiers in microbiology · 2023
    Article
  2. Article
  3. Article
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  7. Characteristics of Shigatoxin-ProducingFrontiers in microbiology · 2017
    Article
  8. Named entity linking of geospatial and host metadata in GenBank for advancing biomedical research.Database : the journal of biological databases and curation · 2017
    Article
  9. Article
  10. Article
  11. Review
  12. Article
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  15. Predicting the public health benefit of vaccinating cattle against Escherichia coli O157.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  16. Article
  17. Article
  18. Article
  19. Article
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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

12 authors at 7 institutions in 2 countries.

James L BonoUnited States Department of Agriculture, Agricultural Research Service, US Meat Animal Research Center, Clay Center, Nebraska, USA.
Timothy P L Smith
James E Keen
Gregory P Harhay
Tara G McDaneld
Robert E Mandrell
Woo Kyung Jung
Thomas E Besser
Peter Gerner-Smidt
Martina Bielaszewska
Helge Karch
Michael L Clawson
Agricultural Research Service · USUniversity of Münster · DEWashington State University · USCenters for Disease Control and Prevention · USRoman L. Hruska U.S. Meat Animal Research Center · USUnited States Department of Agriculture · USWestern Regional Research Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cattle are a major reservoir for Shiga toxin-producing Escherichia coli O157 (STEC O157) and harbor multiple genetic subtypes that do not all associate with human disease. STEC O157 evolved from an E. coli O55:H7 progenitor; however, a lack of genome sequence has hindered investigations on the divergence of human- and/or cattle-associated subtypes. Our goals were to 1) identify nucleotide polymorphisms for STEC O157 genetic subtype detection, 2) determine the phylogeny of STEC O157 genetic subtypes using polymorphism-derived genotypes and a phage insertion typing system, and 3) compare polymorphism-derived genotypes identified in this study with pulsed field gel electrophoresis (PFGE), the current gold standard for evaluating STEC O157 diversity. Using 762 nucleotide polymorphisms that were originally identified through whole-genome sequencing of 189 STEC O157 human- and cattle-isolated strains, we genotyped a collection of 426 STEC O157 strains. Concatenated polymorphism alleles defined 175 genotypes that were tagged by a minimal set of 138 polymorphisms. Eight major lineages of STEC O157 were identified, of which cattle are a reservoir for seven. Two lineages regularly harbored by cattle accounted for the majority of human disease in this study, whereas another was rarely represented in humans and may have evolved toward reduced human virulence. Notably, cattle are not a known reservoir for E. coli O55:H7 or STEC O157:H(-) (the first lineage to diverge within the STEC O157 serogroup), which both cause human disease. This result calls into question how cattle may have originally acquired STEC O157. The polymorphism-derived genotypes identified in this study did not surpass PFGE diversity assessed by BlnI and XbaI digestions in a subset of 93 strains. However, our results show that they are highly effective in assessing the evolutionary relatedness of epidemiologically unrelated STEC O157 genetic subtypes, including those associated with the cattle reservoir and human disease.

Indexed as

PhylogenyAllelesAnimalsCattleDNA, BacterialElectrophoresis, Gel, Pulsed-FieldEscherichia coli O157Evolution, MolecularGenotypeGenotyping TechniquesHumansModels, GeneticPolymorphism, GeneticReproducibility of ResultsShiga ToxinDNA, BacterialShiga Toxin

Identifiers

PMID22355013
PMCPMC3408066
OpenAlexW2165381003

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.