Evidence map›Paper›PMID 36002802›Full record

ArticleBMC infectious diseases2022

Epidemiology and genomic analysis of Klebsiella oxytoca from a single hospital network in Australia.

James Stewart, Louise M Judd, Adam Jenney, Kathryn E Holt, Kelly L Wyres, Jane Hawkey

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 33 citations in OpenAlex.

  1. Global genomic landscape of theNew microbes and new infections · 2026
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  8. Detection of ESBL-producingJournal of clinical microbiology · 2025
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  11. Multiple regional outbreaks caused by global and local VIM-producing Klebsiella pneumoniae clones in Poland, 2006-2019.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
    Article
  12. Article
  13. Article
  14. Genome assembly ofFrontiers in microbiology · 2025
    Article
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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 at 2 institutions in 2 countries.

James StewartDepartment of Infectious Diseases, Cairns Hospital, Cairns, QLD, 4870, Australia.
Louise M JuddDepartment of Infectious Diseases, Central Clinical School, Monash University, Melbourne, VIC, 3004, Australia.
Adam JenneyDepartment of Infectious Diseases, Central Clinical School, Monash University, Melbourne, VIC, 3004, Australia. a.jenney@alfred.org.au.
Kathryn E HoltDepartment of Infectious Diseases, Central Clinical School, Monash University, Melbourne, VIC, 3004, Australia.
Kelly L Wyres *Department of Infectious Diseases, Central Clinical School, Monash University, Melbourne, VIC, 3004, Australia.
Jane Hawkey *Department of Infectious Diseases, Central Clinical School, Monash University, Melbourne, VIC, 3004, Australia. jane.hawkey@monash.edu.
Monash University · AUCairns Hospital · AU

Funding

Alfred Hospital Research Trust Small Project Grant T11938Bill and Melinda Gates Foundation OPP1175797National Health and Medical Research Council,Australia APP1176192
6 · The paper itself

Abstract

backgroundInfections caused by Klebsiella oxytoca are the second most common cause of Klebsiella infections in humans. Most studies have focused on K. oxytoca outbreaks and few have examined the broader clinical context of K. oxytoca.

methodsHere, we collected all clinical isolates identified as K. oxytoca in a hospital microbiological diagnostic lab across a 15-month period (n = 239). Whole genome sequencing was performed on a subset of 92 isolates (all invasive, third-generation cephalosporin resistant (3GCR) and non-urinary isolates collected > 48 h after admission), including long-read sequencing on a further six isolates with extended-spectrum beta-lactamase or carbapenemase genes.

resultsThe majority of isolates were sensitive to antimicrobials, however 22 isolates were 3GCR, of which five were also carbapenem resistant. Genomic analyses showed those identified as K. oxytoca by the clinical laboratory actually encompassed four distinct species (K. oxytoca, Klebsiella michiganensis, Klebsiella grimontii and Klebsiella pasteurii), referred to as the K. oxytoca species complex (KoSC). There was significant diversity within the population, with only 10/67 multi-locus sequence types (STs) represented by more than one isolate. Strain transmission was rare, with only one likely event identified. Six isolates had extended spectrum beta-lactamase (bla

conclusionWhilst antimicrobial resistance was rare, the resistance plasmids were similar to those found in other Enterobacterales, demonstrating that KoSC has access to the same plasmid reservoir and thus there is potential for multi-drug resistance. Further genomic studies are required to improve our understanding of the KoSC population and facilitate investigation into the attributes of successful nosocomial isolates.

Indexed as

Klebsiella InfectionsKlebsiella oxytocaAnti-Bacterial Agentsbeta-LactamasesDrug Resistance, Multiple, BacterialGenomicsHospitalsHumansKlebsiella pneumoniaeMicrobial Sensitivity TestsPlasmidsAnti-Bacterial Agentsbeta-LactamasesCarbapenemaseESBLGenomicsKleboxymycinKlebsiella oxytoca

Identifiers

PMID36002802
PMCPMC9400251
OpenAlexW4293105711

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.