Evidence map›Paper›PMID 27733632›Full record

ArticleJournal of clinical microbiology2016

Exploiting Bacterial Whole-Genome Sequencing Data for Evaluation of Diagnostic Assays: Campylobacter Species Identification as a Case Study.

Melissa J Jansen van Rensburg, Craig Swift, Alison J Cody, Claire Jenkins, Martin C J Maiden

Open access · hybridAbstract read
In one paragraph

Article in Journal of clinical microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
5.2field-weighted citation impact, top 6% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Economic evaluation of whole genome sequencing for pathogen identification and surveillance - results of case studies in Europe and the Americas 2016 to 2019.Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2021
    Article
  4. Article
  5. Review
  6. Molecular Assay Validation Using Genomic Sequence Databases.Journal of clinical microbiology · 2016
    Article
  7. 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

5 authors at 1 institution in 1 country.

Melissa J Jansen van RensburgDepartment of Zoology, University of Oxford, Oxford, United Kingdom.
Craig SwiftNIHR Health Protection Research Unit in Gastrointestinal Infections, University of Oxford, Oxford, United Kingdom.
Alison J CodyDepartment of Zoology, University of Oxford, Oxford, United Kingdom.
Claire JenkinsNIHR Health Protection Research Unit in Gastrointestinal Infections, University of Oxford, Oxford, United Kingdom.
Martin C J MaidenDepartment of Zoology, University of Oxford, Oxford, United Kingdom martin.maiden@zoo.ox.ac.uk.ORCID 0000-0001-6321-5138
University of Liverpool · GB

Funding

Wellcome Trust 087622
6 · The paper itself

Abstract

The application of whole-genome sequencing (WGS) to problems in clinical microbiology has had a major impact on the field. Clinical laboratories are now using WGS for pathogen identification, antimicrobial susceptibility testing, and epidemiological typing. WGS data also represent a valuable resource for the development and evaluation of molecular diagnostic assays, which continue to play an important role in clinical microbiology. To demonstrate this application of WGS, this study used publicly available genomic data to evaluate a duplex real-time PCR (RT-PCR) assay that targets mapA and ceuE for the detection of Campylobacter jejuni and Campylobacter coli, leading global causes of bacterial gastroenteritis. In silico analyses of mapA and ceuE primer and probe sequences from 1,713 genetically diverse C. jejuni and C. coli genomes, supported by RT-PCR testing, indicated that the assay was robust, with 1,707 (99.7%) isolates correctly identified. The high specificity of the mapA-ceuE assay was the result of interspecies diversity and intraspecies conservation of the target genes in C. jejuni and C. coli Rare instances of a lack of specificity among C. coli isolates were due to introgression in mapA or sequence diversity in ceuE The results of this study illustrate how WGS can be exploited to evaluate molecular diagnostic assays by using publicly available data, online databases, and open-source software.

Indexed as

Bacterial ProteinsBase SequenceCampylobacter coliCampylobacter InfectionsCampylobacter jejuniCarrier ProteinsGastroenteritisGenome, BacterialHumansIron-Binding ProteinsMembrane ProteinsMolecular Diagnostic TechniquesReal-Time Polymerase Chain ReactionSequence Analysis, DNABacterial ProteinsCarrier ProteinsceuE protein, Campylobacter coliIron-Binding ProteinsmapA protein, Campylobacter jejuniMembrane Proteins

Identifiers

PMID27733632
PMCPMC5121375
OpenAlexW2530411835

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.