Evidence map›Paper›PMID 26230489›Full record

ArticlePLoS genetics2015

A Year of Infection in the Intensive Care Unit: Prospective Whole Genome Sequencing of Bacterial Clinical Isolates Reveals Cryptic Transmissions and Novel Microbiota.

David J Roach, Joshua N Burton, Choli Lee, Bethany Stackhouse, Susan M Butler-Wu, Brad T Cookson, Jay Shendure, Stephen J Salipante

Erratum issued Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT03532438 (Whole Genome Sequencing of Nontuberculous Mycobacterium), which is not on this map. Cited by 116 papers.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed
14.2field-weighted citation impact, top 1% 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.

NCT03532438 unknown statusnot on this mapstarted 2018, after this paper: background citation

Whole Genome Sequencing of Nontuberculous Mycobacterium (NTM) Derived From Sputum Specimen of NTM Lung Disease Patients Living Together and From Their Environmental Samples

Typeobservational_patient_registrySponsorSeoul National University HospitalRan2018 to 2019Enrolled6ConditionsNontuberculous Mycobacterium Infection, Whole Genome Sequencing
3 · Its place in the literature

Who cites it

116 citing papers in PubMed, 189 citations in OpenAlex.

  1. Article
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  5. Description of two novelbioRxiv : the preprint server for biology · 2024
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  9. Tad pili contribute to the virulence and biofilm formation of virulentFrontiers in cellular and infection microbiology · 2024
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  11. Review
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  13. Tetracycline-modifying enzyme SmTetX from Stenotrophomonas maltophilia.Acta crystallographica. Section F, Structural biology communications · 2023
    Article
  14. Article
  15. First Isolation ofPathogens (Basel, Switzerland) · 2022
    Article
  16. Article
  17. The genus Serratia revisited by genomics.Nature communications · 2022
    Article
  18. Article
  19. Evolution of cefiderocol resistance inJAC-antimicrobial resistance · 2022
    Article
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

David J RoachDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Joshua N BurtonDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Choli LeeDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Bethany StackhouseDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Susan M Butler-WuDepartment of Laboratory Medicine, University of Washington, Seattle, Washington, United States of America.
Brad T CooksonDepartment of Laboratory Medicine, University of Washington, Seattle, Washington, United States of America; Department of Microbiology, University of Washington, Seattle, Washington, United States of America.
Jay ShendureDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Stephen J SalipanteDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America; Department of Laboratory Medicine, University of Washington, Seattle, Washington, United States of America.
University of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial whole genome sequencing holds promise as a disruptive technology in clinical microbiology, but it has not yet been applied systematically or comprehensively within a clinical context. Here, over the course of one year, we performed prospective collection and whole genome sequencing of nearly all bacterial isolates obtained from a tertiary care hospital's intensive care units (ICUs). This unbiased collection of 1,229 bacterial genomes from 391 patients enables detailed exploration of several features of clinical pathogens. A sizable fraction of isolates identified as clinically relevant corresponded to previously undescribed species: 12% of isolates assigned a species-level classification by conventional methods actually qualified as distinct, novel genomospecies on the basis of genomic similarity. Pan-genome analysis of the most frequently encountered pathogens in the collection revealed substantial variation in pan-genome size (1,420 to 20,432 genes) and the rate of gene discovery (1 to 152 genes per isolate sequenced). Surprisingly, although potential nosocomial transmission of actively surveilled pathogens was rare, 8.7% of isolates belonged to genomically related clonal lineages that were present among multiple patients, usually with overlapping hospital admissions, and were associated with clinically significant infection in 62% of patients from which they were recovered. Multi-patient clonal lineages were particularly evident in the neonatal care unit, where seven separate Staphylococcus epidermidis clonal lineages were identified, including one lineage associated with bacteremia in 5/9 neonates. Our study highlights key differences in the information made available by conventional microbiological practices versus whole genome sequencing, and motivates the further integration of microbial genome sequencing into routine clinical care.

Indexed as

Intensive Care UnitsAdolescentAdultAgedAged, 80 and overBacteriaBacterial InfectionsBacterial Typing TechniquesBiodiversityCross InfectionDNA, BacterialFemaleGenetic VariationGenome, BacterialHumansInfantDNA, Bacterial

Identifiers

PMID26230489
PMCPMC4521703
OpenAlexW991210025

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.