Evidence map›Paper›PMID 35803292›Full record

ArticleThe Lancet. Microbe2022

Threshold-free genomic cluster detection to track transmission pathways in health-care settings: a genomic epidemiology analysis.

Shawn E Hawken, Rachel D Yelin, Karen Lolans, Ali Pirani, Robert A Weinstein, Michael Y Lin, Mary K Hayden, Evan S Snitkin, CDC Prevention Epicenter Program

Open access · goldAbstract read
In one paragraph

Article in The Lancet. Microbe, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  7. Emergence ofbioRxiv : the preprint server for biology · 2025
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  9. Observational
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  12. Evidence ofMicrobial genomics · 2024
    Article
  13. Article
  14. Transmission of Carbapenem-Resistant Klebsiella pneumoniae in US Hospitals.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
    Article
  15. 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

9 authors at 2 institutions in 1 country.

Shawn E HawkenDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, USA.
Rachel D YelinDepartment of Internal Medicine, Division of Infectious Diseases, Rush University Medical Center, Chicago, IL, USA.
Karen LolansDepartment of Internal Medicine, Division of Infectious Diseases, Rush University Medical Center, Chicago, IL, USA.
Ali PiraniDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, USA.
Robert A WeinsteinDepartment of Internal Medicine, Division of Infectious Diseases, Rush University Medical Center, Chicago, IL, USA.
Michael Y LinDepartment of Internal Medicine, Division of Infectious Diseases, Rush University Medical Center, Chicago, IL, USA.
Mary K HaydenDepartment of Internal Medicine, Division of Infectious Diseases, Rush University Medical Center, Chicago, IL, USA.
Evan S SnitkinDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, USA; Internal Medicine Division of Infectious Diseases, University of Michigan Medical School, Ann Arbor, MI, USA. Electronic address: esnitkin@umich.edu.
CDC Prevention Epicenter Program
Rush University Medical Center · USUniversity of Michigan–Ann Arbor · US

Funding

Training Program in Translational ResearchT32GM113900 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIEBERMAN, ANDREW P, NIKOLOVSKA-COLESKA, ZANETA · 2016 to 2020
$991k
NCEZID CDC HHS U54 CK000481NCEZID CDC HHS U54 CK000607NIGMS NIH HHS T32 GM113900
6 · The paper itself

Abstract

backgroundA crucial barrier to the routine application of whole-genome sequencing (WGS) for infection prevention is the insufficient criteria for determining whether a genomic linkage is consistent with transmission within the facility. We evaluated the use of single-nucleotide variant (SNV) thresholds, as well as a novel threshold-free approach, for inferring transmission linkages in a high-transmission setting.

methodsWe did a retrospective genomic epidemiology analysis of samples previously collected in the context of an intervention study at a long-term acute care hospital in the USA. We performed WGS on 435 isolates of Klebsiella pneumoniae harbouring the bla

findingsOur analysis showed that the standard approach of using an SNV threshold to define transmission would lead to false-positive and false-negative inferences. False-positive inferences were driven by the frequent importation of closely related strains, which were presumably linked via transmission at connected health-care facilities. False-negative inferences stemmed from the diversity of colonising populations that were spread among patients, with multiple examples of hypermutator strain emergence within patients and, as a result, putative transmission links separated by large genetic distances. Motivated by limitations of an SNV threshold, we implemented a novel threshold-free transmission cluster inference approach, in which each of the acquired KPC-Kp isolates were linked back to the imported KPC-Kp isolate with which it shared the most variants. This approach yielded clusters that varied in levels of genetic diversity but where 105 (81%) of 129 unique strain acquisition events were associated with epidemiological links in the hospital. Of 100 patients who acquired KPC-Kp isolates that were included in a cluster, 47 could be linked to a single patient who was positive for KPC-Kp at admission, compared with 31 and 25 using 10 SNV and 20 SNV thresholds, respectively. Holistic examination of clusters highlighted extensive variation in the magnitude of onward transmission stemming from more than 100 importation events and revealed patterns in cluster propagation that could inform improvements to infection prevention strategies.

interpretationOur results show how the integration of culture surveillance data into genomic analyses can overcome limitations of cluster detection based on SNV-thresholds and improve the ability to track pathways of pathogen transmission in health-care settings.

fundingUS Center for Disease Control and Prevention and University of Michigan.

Indexed as

Klebsiella InfectionsDisease OutbreaksGenomicsHumansKlebsiella pneumoniaeRetrospective Studies

Identifiers

PMID35803292
PMCPMC9869340
OpenAlexW4283833852

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.