Evidence map›Paper›PMID 26922068›Full record

ArticleEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2016

Comparison of MALDI-TOF MS and AFLP for strain typing of ESBL-producing Escherichia coli.

J Veenemans, M Welker, A van Belkum, M C Saccomani, V Girard, A Pettersson, C Verhulst, M Kluytmans-Vandenbergh, J Kluytmans

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Article in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Use of MALDI-TOF mass spectrometry to detect nosocomial outbreaks of Serratia marcescens and Citrobacter freundii.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2019
    Article
  7. Article
  8. 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.

J VeenemansLaboratory for Microbiology and Infection Control, Amphia Hospital, Breda, 4800 RK, The Netherlands. Jacobien.veenemans@gmail.com.
M WelkerBioMerieux, Microbiology R&D, La Balme Les Grottes, France.
A van BelkumBioMerieux, Microbiology R&D, La Balme Les Grottes, France.
M C SaccomaniBioMerieux, Microbiology R&D, La Balme Les Grottes, France.
V GirardBioMerieux, Microbiology R&D, La Balme Les Grottes, France.
A PetterssonDepartment for Medical Microbiology and Infection Control, VU University Medical Centre, Amsterdam, The Netherlands.
C VerhulstLaboratory for Microbiology and Infection Control, Amphia Hospital, Breda, 4800 RK, The Netherlands.
M Kluytmans-VandenberghLaboratory for Microbiology and Infection Control, Amphia Hospital, Breda, 4800 RK, The Netherlands.
J KluytmansLaboratory for Microbiology and Infection Control, Amphia Hospital, Breda, 4800 RK, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Typing of bacterial isolates using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) potentially provides an efficient on-site method to monitor the spread of antibiotic-resistant bacteria and rapidly detect outbreaks. We compared MALDI-MS typing results to those of amplified fragment length polymorphism (AFLP) in a collection of 52 ESBL-producing Escherichia coli, isolated in a Dutch nursing home with an on-going outbreak of ST131 E. coli. Specific MALDI types were defined based on spectral data from four replicate colony samples of isolates grown on Columbia agar using multivariate statistical procedures. Type-specific superspectra were computed for four E .coli MALDI-types and tested for the potential of rapid and automated typing. The effect of different incubation conditions on typing performance was tested by analysing five isolates incubated for 24 h and 48 h on five different media. Types defined based on MALDI spectra were largely in agreement with the AFLP results, although some MALDI types comprised of more than one AFLP type. In particular, isolates belonging to ST131 showed distinct mass patterns. The proportion of isolates correctly assigned was substantially lower for isolates incubated on Sabouraud-dextrose and Drigalski agars for 24 h, and for those incubated for 48 h (all media). Our results show that the identification of type-specific peaks potentially allows direct typing of isolates belonging to specific clonal lineages. Both incubation time and media affected type assignment, suggesting that there is a need for a careful standardization of incubation time and culturing conditions when developing MALDI-typing schemes for E. coli.

Indexed as

Amplified Fragment Length Polymorphism AnalysisSpectrometry, Mass, Matrix-Assisted Laser Desorption-Ionizationbeta-LactamasesCluster AnalysisEscherichia coliEscherichia coli InfectionsHumansReproducibility of Resultsbeta-Lactamases

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Registered trials

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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.