Evidence map›Paper›PMID 26442781›Full record

ArticleScientific reports2015

Whole Genome Sequencing demonstrates that Geographic Variation of Escherichia coli O157 Genotypes Dominates Host Association.

Norval J C Strachan, Ovidiu Rotariu, Bruno Lopes, Marion MacRae, Susan Fairley, Chad Laing, Victor Gannon, Lesley J Allison, Mary F Hanson, Tim Dallman and 7 more

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Ruminant-dense environments increase risk of Shiga toxin-producingmedRxiv : the preprint server for health sciences · 2024
    Article
  6. CommensalAnimals : an open access journal from MDPI · 2023
    Article
  7. Article
  8. Article
  9. Prevalence and Implications of Shiga Toxin-ProducingPathogens (Basel, Switzerland) · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Genome Sequence Analysis and Characterization of Shiga Toxin 2 Production byFrontiers in cellular and infection microbiology · 2022
    Article
  14. Article
  15. Genomic Epidemiology of Shiga Toxin-ProducingAnimals : an open access journal from MDPI · 2021
    Article
  16. Review
  17. Article
  18. Monitoring the Microevolution ofFrontiers in microbiology · 2021
    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

17 authors.

Norval J C StrachanSchool of Biological Sciences, The University of Aberdeen, Cruickshank Building. St Machar Drive, Aberdeen, Scotland, United Kingdom, AB24 3UU.
Ovidiu RotariuSchool of Biological Sciences, The University of Aberdeen, Cruickshank Building. St Machar Drive, Aberdeen, Scotland, United Kingdom, AB24 3UU.
Bruno LopesSchool of Medicine and Dentistry, The University of Aberdeen, Foresterhill, Aberdeen, Scotland, United Kingdom, AB25 2ZD.
Marion MacRaeSchool of Medicine and Dentistry, The University of Aberdeen, Foresterhill, Aberdeen, Scotland, United Kingdom, AB25 2ZD.
Susan FairleyCentre for Genome Enabled Biology, 23 St Machar Drive, Aberdeen, Scotland, United Kingdom, AB24 3UU.
Chad LaingLaboratory for Foodborne Zoonoses, Public Health Agency of Canada, 225089 Township Road 9-1 (Box 640), Lethbridge, Alberta, Canada, T1J 3Z4.
Victor GannonLaboratory for Foodborne Zoonoses, Public Health Agency of Canada, 225089 Township Road 9-1 (Box 640), Lethbridge, Alberta, Canada, T1J 3Z4.
Lesley J AllisonScottish E. coli O157/VTEC Reference Laboratory, NHS Lothian, Royal Infirmary of Edinburgh, 51 Little France Crescent, Edinburgh, Scotland, United Kingdom, EH16 4SA.
Mary F HansonScottish E. coli O157/VTEC Reference Laboratory, NHS Lothian, Royal Infirmary of Edinburgh, 51 Little France Crescent, Edinburgh, Scotland, United Kingdom, EH16 4SA.
Tim DallmanPublic Health England, 61 Colindale Avenue, London, United Kingdom, NW9 5EQ.
Philip AshtonPublic Health England, 61 Colindale Avenue, London, United Kingdom, NW9 5EQ.
Eelco FranzNational Institute for Public Health and the Environment (RIVM), Centre for Infectious Disease Control (CIb), P.O. Box 1, 3720 BA Bilthoven, the Netherlands.
Angela H A M van HoekNational Institute for Public Health and the Environment (RIVM), Centre for Infectious Disease Control (CIb), P.O. Box 1, 3720 BA Bilthoven, the Netherlands.
Nigel P FrenchmEpiLab, Infectious Disease Research Centre, Institute of Veterinary Animal and Biomedical Sciences, Massey University, Palmerston North, New Zealand.
Tessy GeorgemEpiLab, Infectious Disease Research Centre, Institute of Veterinary Animal and Biomedical Sciences, Massey University, Palmerston North, New Zealand.
Patrick J BiggsmEpiLab, Infectious Disease Research Centre, Institute of Veterinary Animal and Biomedical Sciences, Massey University, Palmerston North, New Zealand.
Ken J ForbesSchool of Medicine and Dentistry, The University of Aberdeen, Foresterhill, Aberdeen, Scotland, United Kingdom, AB25 2ZD.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic variation in an infectious disease pathogen can be driven by ecological niche dissimilarities arising from different host species and different geographical locations. Whole genome sequencing was used to compare E. coli O157 isolates from host reservoirs (cattle and sheep) from Scotland and to compare genetic variation of isolates (human, animal, environmental/food) obtained from Scotland, New Zealand, Netherlands, Canada and the USA. Nei's genetic distance calculated from core genome single nucleotide polymorphisms (SNPs) demonstrated that the animal isolates were from the same population. Investigation of the Shiga toxin bacteriophage and their insertion sites (SBI typing) revealed that cattle and sheep isolates had statistically indistinguishable rarefaction profiles, diversity and genotypes. In contrast, isolates from different countries exhibited significant differences in Nei's genetic distance and SBI typing. Hence, after successful international transmission, which has occurred on multiple occasions, local genetic variation occurs, resulting in a global patchwork of continental and trans-continental phylogeographic clades. These findings are important for three reasons: first, understanding transmission and evolution of infectious diseases associated with multiple host reservoirs and multi-geographic locations; second, highlighting the relevance of the sheep reservoir when considering farm based interventions; and third, improving our understanding of why human disease incidence varies across the world.

Indexed as

GenomePhylogeographyAnimalsBacteriophagesCattleEscherichia coli InfectionsEscherichia coli O157Genetic VariationHigh-Throughput Nucleotide SequencingHost-Pathogen InteractionsHumansNew ZealandPolymorphism, Single NucleotideSheep

Identifiers

PMID26442781
PMCPMC4595763

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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.