Evidence map›Paper›PMID 27005433›Full record

SynthesisBMC medicine2016

Interpreting whole genome sequencing for investigating tuberculosis transmission: a systematic review.

Hollie-Ann Hatherell, Caroline Colijn, Helen R Stagg, Charlotte Jackson, Joanne R Winter, Ibrahim Abubakar

Abstract readSystematic Review
In one paragraph

Synthesis in BMC medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
92citing 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.

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

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

  1. Pooled it
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  3. Effectiveness of interventions for reducing TB incidence in countries with low TB incidence: a systematic review of reviews.European respiratory review : an official journal of the European Respiratory Society · 2019
    Pooled it
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  5. Article
  6. Spatio-temporal patterns of tuberculosis revealed by routineThe Lancet regional health. Western Pacific · 2026
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32 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

6 authors.

Hollie-Ann HatherellCoMPLEX, University College London, London, WC1E 6BT, UK. hollie-ann.hatherell.13@ucl.ac.uk.
Caroline ColijnDepartment of Mathematics, Imperial College London, London, SW7 2AZ, UK.
Helen R StaggCentre for Infectious Disease Epidemiology, Infection and Population Health, University College London, London, WC1E 6JB, UK.
Charlotte JacksonCentre for Infectious Disease Epidemiology, Infection and Population Health, University College London, London, WC1E 6JB, UK.
Joanne R WinterCentre for Infectious Disease Epidemiology, Infection and Population Health, University College London, London, WC1E 6JB, UK.
Ibrahim AbubakarCentre for Infectious Disease Epidemiology, Infection and Population Health, University College London, London, WC1E 6JB, UK.

Funding

Department of Health PDF-2014-07-008Medical Research Council
6 · The paper itself

Abstract

backgroundWhole genome sequencing (WGS) is becoming an important part of epidemiological investigations of infectious diseases due to greater resolution and cost reductions compared to traditional typing approaches. Many public health and clinical teams will increasingly use WGS to investigate clusters of potential pathogen transmission, making it crucial to understand the benefits and assumptions of the analytical methods for investigating the data. We aimed to understand how different approaches affect inferences of transmission dynamics and outline limitations of the methods.

methodsWe comprehensively searched electronic databases for studies that presented methods used to interpret WGS data for investigating tuberculosis (TB) transmission. Two authors independently selected studies for inclusion and extracted data. Due to considerable methodological heterogeneity between studies, we present summary data with accompanying narrative synthesis rather than pooled analyses.

resultsTwenty-five studies met our inclusion criteria. Despite the range of interpretation tools, the usefulness of WGS data in understanding TB transmission often depends on the amount of genetic diversity in the setting. Where diversity is small, distinguishing re-infections from relapses may be impossible; interpretation may be aided by the use of epidemiological data, examining minor variants and deep sequencing. Conversely, when within-host diversity is large, due to genetic hitchhiking or co-infection of two dissimilar strains, it is critical to understand how it arose. Greater understanding of microevolution and mixed infection will enhance interpretation of WGS data.

conclusionsAs sequencing studies have sampled more intensely and integrated multiple sources of information, the understanding of TB transmission and diversity has grown, but there is still much to be learnt about the origins of diversity that will affect inferences from these data. Public health teams and researchers should combine epidemiological, clinical and WGS data to strengthen investigations of transmission.

Indexed as

Genome-Wide Association StudyBacterial Typing TechniquesGenetic VariationGenome, BacterialHumansMycobacterium tuberculosisRecurrenceSequence Analysis, DNATuberculosisSystematic reviewTransmissionTuberculosisWhole genome sequencing

Identifiers

PMID27005433
PMCPMC4804562

What OpenQuestion holds

Textmetadata
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.