Evidence map›Paper›PMID 34517886›Full record

ArticleGenome medicine2021

Whole-genome sequence-informed MALDI-TOF MS diagnostics reveal importance of Klebsiella oxytoca group in invasive infections: a retrospective clinical study.

Aline Cuénod, Daniel Wüthrich, Helena M B Seth-Smith, Chantal Ott, Christian Gehringer, Frédéric Foucault, Roxanne Mouchet, Ali Kassim, Gunturu Revathi, Deborah R Vogt and 19 more

Open access · goldAbstract read
In one paragraph

Article in Genome medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 38 citations in OpenAlex.

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  15. Draft genome assemblies of threeMicrobiology resource announcements · 2024
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  17. Antibiotic resistance surveillance ofEuro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2022
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  19. The effect of sequencing and assembly on the inference of horizontal gene transfer on chromosomal and plasmid phylogenies.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
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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

29 authors at 11 institutions in 5 countries.

Aline CuénodApplied Microbiology Research, Department of Biomedicine, University of Basel, Hebelstrasse 20, 4031, Basel, Switzerland. aline.cuenod@stud.unibas.ch.ORCID 0000-0002-8522-6134
Daniel WüthrichApplied Microbiology Research, Department of Biomedicine, University of Basel, Hebelstrasse 20, 4031, Basel, Switzerland.
Helena M B Seth-SmithApplied Microbiology Research, Department of Biomedicine, University of Basel, Hebelstrasse 20, 4031, Basel, Switzerland.
Chantal OttApplied Microbiology Research, Department of Biomedicine, University of Basel, Hebelstrasse 20, 4031, Basel, Switzerland.
Christian GehringerApplied Microbiology Research, Department of Biomedicine, University of Basel, Hebelstrasse 20, 4031, Basel, Switzerland.
Frédéric FoucaultMabritec AG, Riehen, Switzerland.
Roxanne MouchetMabritec AG, Riehen, Switzerland.
Ali KassimAga Khan University Hospital, Nairobi, Kenya.
Gunturu RevathiAga Khan University Hospital, Nairobi, Kenya.
Deborah R VogtDepartment of Clinical Research, University of Basel and University Hospital Basel, Basel, Switzerland.
Stefanie von FeltenDepartment of Clinical Research, University of Basel and University Hospital Basel, Basel, Switzerland.
Stefano BassettiDivision of Internal Medicine, University Hospital Basel, Basel, Switzerland.
Sarah Tschudin-SutterDivision of Infectious Diseases and Hospital Epidemiology, University Hospital Basel, Basel, Switzerland.
Timm HettichDivision of Instrumental Analytics, School of Applied Sciences (FHNW), Muttenz, Switzerland.
Götz SchlotterbeckDivision of Instrumental Analytics, School of Applied Sciences (FHNW), Muttenz, Switzerland.
Christina HombergerApplied Microbiology Research, Department of Biomedicine, University of Basel, Hebelstrasse 20, 4031, Basel, Switzerland.
Carlo CasanovaInstitute for Infectious Diseases, University of Bern, Bern, Switzerland.
Jacob Moran-GiladFaculty of Health Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel.
Orli SagiFaculty of Health Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel.
Belén Rodríguez-SánchezHospital General Universitario Gregorio Marañón, Madrid, Spain.
Franco MüllerLabor Team W AG, Goldach, Switzerland.
Martina AerniLabor Team W AG, Goldach, Switzerland.
Valeria GaiaServizio di microbiologia EOLAB, Ente Ospedaliero Cantonale, Bellinzona, Switzerland.
Helke van DesselDepartment of Medical Microbiology, Maastricht University Medical Center, Maastricht, the Netherlands.
Greetje A KampingaDepartment of Medical Microbiology & Infection prevention, University of Groningen, Groningen, the Netherlands.
Claudia MüllerLaborgemeinschaft 1, Zurich, Switzerland.
Claudia DaubenbergerSwiss Tropical and Public Health Institute, Basel, Switzerland.
Valentin PflügerMabritec AG, Riehen, Switzerland.
Adrian EgliApplied Microbiology Research, Department of Biomedicine, University of Basel, Hebelstrasse 20, 4031, Basel, Switzerland. adrian.egli@usb.ch.
University of Basel · CHAga Khan University Hospital Nairobi · KEBen-Gurion University of the Negev · ILSIB Swiss Institute of Bioinformatics · CHUniversity Hospital of Basel · CHEnte Ospedaliero Cantonale · CHHospital General Universitario Gregorio Marañón · ESMaastricht University · NLSwiss Tropical and Public Health Institute · CHUniversity Medical Center Groningen · NLUniversity of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKlebsiella spp. are opportunistic pathogens which can cause severe infections, are often multi-drug resistant and are a common cause of hospital-acquired infections. Multiple new Klebsiella species have recently been described, yet their clinical impact and antibiotic resistance profiles are largely unknown. We aimed to explore Klebsiella group- and species-specific clinical impact, antimicrobial resistance (AMR) and virulence.

methodsWe analysed whole-genome sequence data of a diverse selection of Klebsiella spp. isolates and identified resistance and virulence factors. Using the genomes of 3594 Klebsiella isolates, we predicted the masses of 56 ribosomal subunit proteins and identified species-specific marker masses. We then re-analysed over 22,000 Matrix-Assisted Laser Desorption Ionization - Time Of Flight (MALDI-TOF) mass spectra routinely acquired at eight healthcare institutions in four countries looking for these species-specific markers. Analyses of clinical and microbiological endpoints from a subset of 957 patients with infections from Klebsiella species were performed using generalized linear mixed-effects models.

resultsOur comparative genomic analysis shows group- and species-specific trends in accessory genome composition. With the identified species-specific marker masses, eight Klebsiella species can be distinguished using MALDI-TOF MS. We identified K. pneumoniae (71.2%; n = 12,523), K. quasipneumoniae (3.3%; n = 575), K. variicola (9.8%; n = 1717), "K. quasivariicola" (0.3%; n = 52), K. oxytoca (8.2%; n = 1445), K. michiganensis (4.8%; n = 836), K. grimontii (2.4%; n = 425) and K. huaxensis (0.1%; n = 12). Isolates belonging to the K. oxytoca group, which includes the species K. oxytoca, K. michiganensis and K. grimontii, were less often resistant to 4th-generation cephalosporins than isolates of the K. pneumoniae group, which includes the species K. pneumoniae, K. quasipneumoniae, K. variicola and "K. quasivariicola" (odds ratio = 0.17, p < 0.001, 95% confidence interval [0.09,0.28]). Within the K. pneumoniae group, isolates identified as K. pneumoniae were more often resistant to 4th-generation cephalosporins than K. variicola isolates (odds ratio = 2.61, p = 0.003, 95% confidence interval [1.38,5.06]). K. oxytoca group isolates were found to be more likely associated with invasive infection to primary sterile sites than K. pneumoniae group isolates (odds ratio = 2.39, p = 0.0044, 95% confidence interval [1.05,5.53]).

conclusionsCurrently misdiagnosed Klebsiella spp. can be distinguished using a ribosomal marker-based approach for MALDI-TOF MS. Klebsiella groups and species differed in AMR profiles, and in their association with invasive infection, highlighting the importance for species identification to enable effective treatment options.

Indexed as

Spectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationWhole Genome SequencingAnti-Bacterial AgentsDrug Resistance, Multiple, BacterialFemaleGenome, BacterialHumansKlebsiella InfectionsKlebsiella oxytocaKlebsiella pneumoniaeMaleRetrospective StudiesSpecies SpecificityVirulenceVirulence FactorsAnti-Bacterial AgentsVirulence FactorsAntimicrobial resistanceInvasive infectionsKlebsiella spp.MALDI-TOF MSSpecies identification

Identifiers

PMID34517886
PMCPMC8438989
OpenAlexW3200626615

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