Evidence map›Paper›PMID 30514209›Full record

ArticleBMC genomics2018

Evaluation of whole-genome sequencing for outbreak detection of Verotoxigenic Escherichia coli O157:H7 from the Canadian perspective.

Jillian Rumore, Lorelee Tschetter, Ashley Kearney, Rima Kandar, Rachel McCormick, Matthew Walker, Christy-Lynn Peterson, Aleisha Reimer, Celine Nadon

Abstract readEvaluation Study
In one paragraph

Article in BMC genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
–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

38 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. A new suspect:Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2026
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  9. A multi-provincial outbreak ofEpidemiology and infection · 2024
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  10. Article
  11. Review
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  16. Transforming Shiga toxin-producingFrontiers in microbiology · 2023
    Article
  17. Article
  18. Article
  19. Article
  20. Resistance and Pathogenicity ofVeterinary sciences · 2022
    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

9 authors.

Jillian RumoreDivision of Enteric Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB, Canada. jillian.rumore@canada.ca.ORCID http://orcid.org/0000-0001-9509-3905
Lorelee TschetterDivision of Enteric Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB, Canada.
Ashley KearneyDivision of Enteric Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB, Canada.
Rima KandarOutbreak Management Division, Centre for Foodborne, Environmental and Zoonotic Infectious Diseases, Public Health Agency of Canada, Guelph, ON, Canada.
Rachel McCormickOutbreak Management Division, Centre for Foodborne, Environmental and Zoonotic Infectious Diseases, Public Health Agency of Canada, Guelph, ON, Canada.
Matthew WalkerDivision of Enteric Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB, Canada.
Christy-Lynn PetersonDivision of Enteric Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB, Canada.
Aleisha ReimerDivision of Enteric Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB, Canada.
Celine NadonDivision of Enteric Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRapid and accurate identification of Verotoxigenic Escherichia coli (VTEC) O157:H7 is dependent on well-established, standardized and highly discriminatory typing methods. Currently, conventional subtyping tests for foodborne bacterial pathogen surveillance are rapidly being replaced with whole-genome sequencing (WGS) in public health laboratories. The capacity of WGS to revolutionize global foodborne disease surveillance has positioned this tool to become the new gold standard; however, to ensure evidence standards for public health decision making can still be achieved, the performance of WGS must be thoroughly validated against current gold standard methods prior to implementation. Here we aim to verify the performance of WGS in comparison to pulsed-field gel electrophoresis (PFGE) and multiple-locus variable-number tandem repeat analysis (MLVA) for eight retrospective outbreaks of VTEC O157:H7 from the Canadian perspective. Since real-time implementation and routine use of WGS in public health laboratories is highly reliant on standardized data analysis tools, we also provide a comparative analysis of two popular methodologies for WGS analyses; an in-house developed single nucleotide variant phylogenomics (SNVPhyl) pipeline and the BioNumerics whole genome multilocus sequence typing (wgMLST) tool. To provide a useful and consistent starting point for examining laboratory-based surveillance data for VTEC O157:H7 in Canada, we also aim to describe the number of genetic differences observed among outbreak-associated isolates.

resultsWGS provided enhanced resolution over traditional subtyping methods, and accurately distinguished outbreak-related isolates from non-outbreak related isolates with high epidemiological concordance. WGS also illuminated potential linkages between sporadic cases of illness and contaminated food, and isolates spanning multiple years. The topologies generated by SNVPhyl and wgMLST were highly congruent with strong statistical support. Few genetic differences were observed among outbreak-related isolates (≤5 SNVs/ < 10 wgMLST alleles) unless the outbreak was suspected to be multi-strain.

conclusionsThis study validates the superiority of WGS and indicates the BioNumerics wgMLST schema is suitable for surveillance and cluster detection of VTEC O157:H7. These findings will provide a useful and consistent starting point for examining WGS data for prospective laboratory-based surveillance of VTEC O157:H7, but however, the data will continue to be interpreted according to context and in combination with epidemiological and food safety evidence to inform public-health decision making in Canada.

Indexed as

CanadaCluster AnalysisDisease OutbreaksDNA, BacterialElectrophoresis, Gel, Pulsed-FieldEscherichia coli InfectionsEscherichia coli O157Genetic VariationHumansMultilocus Sequence TypingPolymorphism, Single NucleotideRetrospective StudiesShiga-Toxigenic Escherichia coliWhole Genome SequencingDNA, BacterialEscherichia coliO157:H7OutbreakSNVPhylVTECwgMLSTWhole genome sequencing

Identifiers

PMID30514209
PMCPMC6278084

What OpenQuestion holds

Textmetadata
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.