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RESEARCH PRODUCT
Comparison of pulsed-field gel electrophoresis and whole-genome-sequencing-based typing confirms the accuracy of pulsed-field gel electrophoresis for the investigation of local Pseudomonas aeruginosa outbreaks
Michelle ThouverezAlexandre MeunierPascal CholleyDidier HocquetMarlène SaugetXavier BertrandBenoît ValotDaniel Martaksubject
Bacterial typingMicrobiology (medical)030501 epidemiologymedicine.disease_causeGenomeDisease Outbreaks03 medical and health sciencesPulsed-field gel electrophoresisHumansMedicinePseudomonas InfectionsTypingPulsed-field gel electrophoresisReference standardsGel electrophoresisWhole genome sequencingGeneticsWhole-genome sequencing0303 health sciencesWhole Genome Sequencing030306 microbiologybusiness.industryPseudomonas aeruginosaOutbreaksReproducibility of ResultsOutbreakGeneral MedicineBacterial Typing TechniquesElectrophoresis Gel Pulsed-FieldEurope[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyInfectious DiseasesPseudomonas aeruginosacgMLST0305 other medical sciencebusinessGenome BacterialMultilocus Sequence Typingdescription
Summary Aim To determine whether pulsed-field gel electrophoresis (PFGE) accurately recognizes isolates belonging to clusters defined by techniques based on whole-genome sequencing (WGS) using Pseudomonas aeruginosa as a model. Methods We selected 65 isolates of ST395 P. aeruginosa isolated in seven European hospitals between 1998 and 2012. Isolates were typed by PFGE and sequenced by WGS. A core genome multi-locus sequence typing (cgMLST) analysis based on 3831 genes was performed with a homemade pipeline. Findings PFGE identified eight pulsotypes and cgMLST differentiated nine clusters and nine singletons. Five cgMLST clusters and pulsotypes (31/65 isolates) coincided perfectly. Isolates without evident epidemiological links grouped by PFGE were separated by cgMLST (16/65 isolates) differentiating cities, suggesting that PFGE should be kept for the investigation of local outbreaks. Importantly, hypermutator isolates still shared the pulsotype with their parents (16/65 isolates), whereas they were not recognized by cgMLST. This shows that PFGE was less affected than WGS-based typing by the accelerated genetic drift that occurs in epidemic P. aeruginosa. Conclusions although WGS-based typing has logically become the new reference standard, we show here that the PFGE can be used with confidence for the investigation of local outbreaks caused by P. aeruginosa.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2020-08-01 | Journal of Hospital Infection |