Evidence map›Paper›PMID 30115606›Full record

ArticleEBioMedicine2018

Harmonized Genome Wide Typing of Tubercle Bacilli Using a Web-Based Gene-By-Gene Nomenclature System.

Thomas A Kohl, Dag Harmsen, Jörg Rothgänger, Timothy Walker, Roland Diel, Stefan Niemann

Abstract read
In one paragraph

Article in EBioMedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

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

  1. Pooled it
  2. Article
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  5. Review
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  7. Article
  8. Challenge Dose Titration in aInternational journal of molecular sciences · 2024
    Article
  9. Article
  10. Performance evaluation of core genome multilocus sequence typing for genotyping of Mycobacterium tuberculosis strains in China: based on multicenter, population-based collection.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2024
    Article
  11. The Recent Transmission and Associated Risk Factor ofInfection and drug resistance · 2024
    Article
  12. Article
  13. Comparative whole-genome sequence analysis ofFrontiers in microbiology · 2023
    Article
  14. Article
  15. Article
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  18. Review
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  20. Snapshot ofGenes · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Thomas A KohlMolecular and Experimental Mycobacteriology, Forschungszentrum Borstel, 23845 Borstel, Germany.
Dag HarmsenDepartment of Periodontology and Restorative Dentistry, University Hospital Münster, 48149 Münster, Germany.
Jörg RothgängerRidom GmbH, 48149 Münster, Germany.
Timothy WalkerNuffield Department of Medicine, University of Oxford, Oxford, UK.
Roland DielInstitute for Epidemiology, Schleswig-Holstein University Hospital, 24105 Kiel, Germany.
Stefan NiemannMolecular and Experimental Mycobacteriology, Forschungszentrum Borstel, 23845 Borstel, Germany; German Center for Infection Research, Borstel Site, 23845 Borstel, Germany. Electronic address: sniemann@fz-borstel.de.

Funding

Medical Research Council MR/J011398/1
6 · The paper itself

Abstract

backgroundGlobal tuberculosis (TB) control is challenged by uncontrolled transmission of Mycobacterium tuberculosis complex (Mtbc) strains, esp. of multidrug (MDR) or extensively resistant (XDR) variants. Precise analysis of transmission networks is the basis to trace outbreak M/XDR clones and improve TB control. However, classical genotyping tools lack discriminatory power due to the high similarity of strains of particular successful lineages, e.g. Beijing or outbreak strains. This can be overcome by whole genome sequencing (WGS) approaches, but these are not yet standardized to facilitate larger investigations encompassing different laboratories or outbreak tracing across borders.

methodsWe established and improved a whole genome gene-by-gene multi locus sequence typing approach encompassing a stable set of core genome genes (cgMLST) and linked it to a web-based nomenclature server (cgMLST.org) facilitating assignment and storage of allele numbers.

findingsWe evaluated and refined a previously suggested cgMLST schema by using a reference strain set (n = 251) reflecting the global diversity of the Mtbc. A set of 2891 genes showed excellent performance with at least 97% of the genes reliably identified in strains of all Mtbc lineages and in discriminating outbreak strains. cgMLST allele numbers were automatically retrieved from and stored at cgMLST.org.

interpretationThe refined cgMLST schema provides high resolution genome-based typing of clinical strains of all Mtbc lineages. Combined with a web-based nomenclature server, it facilitates rapid, high-resolution, and harmonized tracing of clinical Mtbc strains needed for prospective local and global surveillance.

Indexed as

Bacterial Typing TechniquesGenome, BacterialMultilocus Sequence TypingDrug Resistance, BacterialDrug Resistance, MultipleGenotypeInternetMycobacterium tuberculosisPolymorphism, Single NucleotideWhole Genome SequencingCore genome MLSTGenotypingMolecular epidemiologyMycobacterium tuberculosisWhole genome sequencing

Identifiers

PMID30115606
PMCPMC6116475

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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.