Evidence map›Paper›PMID 27194683›Full record

ArticleJournal of clinical microbiology2016

Standard Genotyping Overestimates Transmission of Mycobacterium tuberculosis among Immigrants in a Low-Incidence Country.

David Stucki, Marie Ballif, Matthias Egger, Hansjakob Furrer, Ekkehardt Altpeter, Manuel Battegay, Sara Droz, Thomas Bruderer, Mireia Coscolla, Sonia Borrell and 16 more

Registry-linked trialAbstract 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. It is linked to trial NCT04172025 (Development of a Swiss Surveillance Database for Molecular Epidemiology of Hypervirulent and Multi-drug Resistant Pathogens), which is not on this map. Cited by 63 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 4 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.

NCT04172025 recruitingnot on this mapstarted 2019, after this paper: background citation

Development of a Swiss Surveillance Database for Molecular Epidemiology of Hypervirulent and Multi-drug Resistant Pathogens

TypeobservationalSponsorUniversity Hospital, Basel, SwitzerlandRan2019 to 2029Enrolled10,000ConditionsMultiresistant Bacterial Pathogens, Virulent Bacterial PathogensArmsAnalysis of Bacterial Genome
3 · Its place in the literature

Who cites it

63 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
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  16. Whole genome sequencing improves the discrimination betweenOne health (Amsterdam, Netherlands) · 2023
    Article
  17. Article
  18. Insights into the Complexity of a DormantMicrobiology spectrum · 2022
    Article
  19. Article
  20. Clinical and public health utility of Mycobacterium tuberculosis whole genome sequencing.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2021
    Article

3 more citing papers are in PubMed but not listed here.

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

26 authors.

David StuckiSwiss Tropical and Public Health Institute, Basel, Switzerland.
Marie BallifSwiss Tropical and Public Health Institute, Basel, Switzerland.
Matthias EggerInstitute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
Hansjakob FurrerDepartment of Infectious Diseases, Bern University Hospital, University of Bern, Bern, Switzerland.
Ekkehardt AltpeterDivision of Communicable Diseases, Federal Office of Public Health, Bern, Switzerland.
Manuel BattegayDivision of Infectious Diseases and Hospital Epidemiology, University Hospital Basel, Basel, Switzerland.
Sara DrozMycobacteriology Unit, Institute for Infectious Diseases, University of Bern, Bern, Switzerland.
Thomas BrudererCenter for Laboratory Medicine, St. Gallen, Switzerland.
Mireia CoscollaSwiss Tropical and Public Health Institute, Basel, Switzerland.
Sonia BorrellSwiss Tropical and Public Health Institute, Basel, Switzerland.
Kathrin ZürcherInstitute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
Jean-Paul JanssensDivision of Pneumology, University Hospital Geneva, Geneva, Switzerland.
Alexandra CalmyDivision of Infectious Diseases, University Hospital Geneva, Geneva, Switzerland.
Jesica Mazza StalderDivision of Pneumology, University Hospital Lausanne, Lausanne, Switzerland.
Katia JatonInstitute of Microbiology, University Hospital of Lausanne, Lausanne, Switzerland.
Hans L RiederEpidemiology, Biostatistics, and Prevention Institute, University of Zürich, Zürich, Switzerland.
Gaby E PfyfferDepartment of Medical Microbiology, Luzerner Kantonsspital, Lucerne, Switzerland.
Hans H SiegristADMed Microbiology, La Chaux-de-Fonds, Switzerland.
Matthias HoffmannDivision of Infectious Diseases, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Jan FehrUniversity Hospital Zürich and University of Zürich, Zürich, Switzerland.
Marisa DolinaServizio di Microbiologia EOLAB, Bellinzona, Switzerland.
Reno FreiDivision of Clinical Microbiology, University Hospital Basel, Basel, Switzerland.
Jacques SchrenzelLaboratory of Bacteriology, University Hospitals of Geneva, Geneva, Switzerland.
Erik C BöttgerInstitute of Medical Microbiology, National Center for Mycobacteria, University of Zürich, Zürich, Switzerland.
Sebastien GagneuxSwiss Tropical and Public Health Institute, Basel, Switzerland.
Lukas FennerSwiss Tropical and Public Health Institute, Basel, Switzerland lukas.fenner@ispm.unibe.ch.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immigrants from regions with a high incidence of tuberculosis (TB) are a risk group for TB in low-incidence countries such as Switzerland. In a previous analysis of a nationwide collection of 520 Mycobacterium tuberculosis isolates from 2000 to 2008, we identified 35 clusters comprising 90 patients based on standard genotyping (24-locus mycobacterial interspersed repetitive-unit-variable-number tandem-repeat [MIRU-VNTR] typing and spoligotyping). Here, we used whole-genome sequencing (WGS) to revisit these transmission clusters. Genome-based transmission clusters were defined as isolate pairs separated by ≤12 single nucleotide polymorphisms (SNPs). WGS confirmed 17/35 (49%) MIRU-VNTR typing clusters; the other 18 clusters contained pairs separated by >12 SNPs. Most transmission clusters (3/4) of Swiss-born patients were confirmed by WGS, as opposed to 25% (4/16) of the clusters involving only foreign-born patients. The overall clustering proportion was 17% (90 patients; 95% confidence interval [CI], 14 to 21%) by standard genotyping but only 8% (43 patients; 95% CI, 6 to 11%) by WGS. The clustering proportion was 17% (67/401; 95% CI, 13 to 21%) by standard genotyping and 7% (26/401; 95% CI, 4 to 9%) by WGS among foreign-born patients and 19% (23/119; 95% CI, 13 to 28%) and 14% (17/119; 95% CI, 9 to 22%), respectively, among Swiss-born patients. Using weighted logistic regression, we found weak evidence of an association between birth origin and transmission (adjusted odds ratio of 2.2 and 95% CI of 0.9 to 5.5 comparing Swiss-born patients to others). In conclusion, standard genotyping overestimated recent TB transmission in Switzerland compared to WGS, particularly among immigrants from regions with a high TB incidence, where genetically closely related strains often predominate. We recommend the use of WGS to identify transmission clusters in settings with a low incidence of TB.

Indexed as

Disease Transmission, InfectiousEmigrants and ImmigrantsMolecular TypingAdolescentAdultCluster AnalysisFemaleFollow-Up StudiesGenome, BacterialHumansIncidenceMaleMiddle AgedMolecular EpidemiologyMycobacterium tuberculosisPolymorphism, Single Nucleotide

Identifiers

PMID27194683
PMCPMC4922098

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Registered trials

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.